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Lawrence Berkeley National Laboratory Recent Work

Title REFERENCES TO PHOTOELECTRON SPECTRA OF GASEOUS

Permalink https://escholarship.org/uc/item/3bf9869z

Authors Horne, D.H. Jolly, W.L.

Publication Date 1986-09-01

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This document was prepared as an account of work sponsored by the United States Government. While this document is believed to contain COlTect information, neither the United States Government nor any agency thereof, nor the Regents of the University of California, nor any of their employees, makes any walTanty, express or implied, or assumes any legal responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, proCess, or service by its trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof, or the Regents of the University of California. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof or the Regents of the University of California.

. , References to Ultraviolet Photoelectron Spectra of Gaseous Molecules

By Dorothy H. Horne and William L. Jolly

Materials and Molecular Research Division, Lawrence Berkeley Laboratory,

University of California, Berkeley, California 94720

This report consists of an alphabetical listing of compounds together with Chemical Abstracts references (for the years 1972-1985) to articles describing research in which these compounds are the subject of gas-phase ultraviolet photoelectron spectroscopic studies. The Chemical Abstracts citations are copyrighted by the American Chemical Society and are reproduced here with their permission.

This work was supported by the U.s. Department of Energy under Contract Number DE-AC03-76SF00098. 2

Aceheptlyene and its methyl derivs. 85: 101568b Acenaphthenequinone, naphthalic anhydride, and naphthalimides, MO in relation to 92: 110101r Acenaphthylene photodimers 98: 32119j Acenes 77: 74665g i\ Acenes, substituent effects on 99: 5035u and acetyl halides, MO interpretn. of 80: 76412h Acetaldehyde and 97: 197664b Acetaldehyde and methyl ketones 81 : 2965q Acetaldehyde, , and vapors, spectral dependence of slow-photoelectron generation in 86: 180259y Acetaldehyde, shifts in 84: 179100s Acetals 96: 51524p Acetanilides and oxindole 93: 131966n Acetanilides, steric and inductive effects in 83: 77933c and monomers & dimers 93: 84571t Acetic and 91 : 55907k Acetone 87: 200467r Acetone derivs. 102 : 5518j Acetone and dimethylmercury ions 83: 27113q and related cmpds., ab initio SCF-MO calcns. 77: 158509x Acetophenone derivs. 93: 7141a Acetyl-, chloro-, and vinylpyridines 95: 70612m Acetylacetones & acetoacetic esters, keto-enol tautomerism in relation to 82: 162212r Acetylacetones, keto-enol tautomerism in rel. to 81 : 62869w 89: 120422y Acetylene 88: 37066u Acetylene 97: 91554a Acetylene 98: 9737b Acetylene Me and silyl derivs., n-splittings in, hyperconJugation model for 81 : 8135r Acetylene and related simple mols., calcns. for 103 : 112712k Acetylene derivs. 90: 143940a Acetylene halo and Me derive cations 92: 119218s Acetylene hydroxy derivs. 90: 130186j Acetylene in 100 : 76808y Acetylene or ethylene, effect of transition metals on, MO calcn. of 92: 128187h Acetylene using single radiation source 95: 212565z Acetylene using synChrotron radiation source satellite lines in 102 : 14521g Acetylene using synchrotron radiation source, angle- resolved 97: 171875w Acetylene, angular distribution of 92: 85534z • Acetylene, monoxide, and , threshold 91 : 131730q and methylacetylenes 80: 26425u Acetylenes and vinylacetylenes contg. Group IV elements 97: 92452c Acrole·in 92: 67357q and lanthanide cmpds., satellite phenom. in 86: 24203v Actinide tetrahalides 93: 16413t Acyclic phosphites 88: 81540t 3

Acylaminobutadienes and related cmpds. 89: 107795c Adamantane 82: 162622z Adamantane and adamantanones 89: 120413w Adamantane and bromoadamantane 78: 110005y Adamantane and bromoadamantane 82: 162623a Adamantanes 80: 14133j Adamantanes 87: 21966f Alakli metal chlorides 81 : 8149y Alakli metal halides 86: 36118j Alakli metal vapors, complexities in 85: 12137t Alcs. 77: 133000m Alcs. 84: 16384y Alcs. and hydroperoxides 88: 21512a Aldehyde, linear ketone, and cyclic ketone hydrazones 92: 41083x Aldehydes and aliph. ketones 87: 38356e Aldehydes and ketones 81 : 97496z Aliph. alcs. 99: 104644y Aliph. amines, alcs. and mercaptans, MO in reI. to 80: 8854d Aliph. azines 80: 81803r Aliph. hydrazones 80: 70119w Aliph. 86: 71185a Aliph. hydrocarbons and , -vapor threshold ionizatn. potentials in relation to 99: 130895a Alk. chlorides and at high temp., 88: 143959x Alk. earth 81 : 18823c Alk. earth , uv and x-ray 84: 67555n Alk. earth halides 88: 97129b Alk. earth halides 90: 194806u Alkadiynes, cations in 92: 75507d Alkali halide monomers, dimers and trimers 96: 152060q Alkali iod ides 101 : 200707b Alkali metaborate vapors 93: 84570s & transitn. metal cyano complexes 85: 101846r Alkali metal cyanides in vapor phase 91 : 30142u Alkali metal fluoride vapors, CI in relation to 94: 22572f Alkali metal fluorides 80: 54333f Alkali metal fluorides & alk. earth fluorides 81 : 56355j Alkali metal halide vapors, polemicd 80: 139213s Alkali metal halides 77: 158497s Alkali metal halides 78: 9990r Alkali metal halides 78: 22284h Alkali metal halides 81 : 97501x Alkali metal halides 83: 68731h Alkali metal halides in gaseous state 80: 139211 q Alkali metal halides in gaseous state 81 : 97482s Alkali metal halides in vapor state 81 : 161852s Alkali metal halides, UV 82: 177831r Alkali metal halocobaltates 85: 101657e Alkali metal nitrates in gaseous state 89: 206994y Alkali metal unpolarized atoms 102 : 69715d Alkali metals and their 91 : 201782j Alkali nitrates and metaphosphates and cyanides in vapor states, high-temp. 91 : 166065d Alkali perrhenates in gaseous state 89: 51047r 4

Alkali tetrahaloaluminate vapors 93: 104376p Alkalimetaphosphates in gaseous phase 91 : 81344u Alkanenitriles, & 3-butenenitrile 100: 42314u 89: 89825f Alkanes 77: 26802c n-Alkanes 88: 21853n Alkanes, core-electron relaxation energies and valence-band formation from 86: 63173e Alkanes, electronic absorption spectra of radical cations in relation to 103 : 141374g Alkanes, and methylsilanes, vs. MO calcns. 99: 175862d and 89: 214534p (Alkene) tetracarbonyl cmpds. 91 : 131712k , , and 85: 192073a Alkenes, ionization potentials in relation to 88: 37068w Alkenyl and alkyl free radicals 100 : 200373u Alkenylsilanes 90: 167475d Alkoxyphenalenones, MO in relation to 91 : 38376u Alkyl Ph , sulfoxides and sulfones, conformation in relation to 95: 6339a Alkyl aryl ethers and sulfides, conformation in reI. to 82: 57415m Alkyl aryl 95: 168370f Alkyl fluorides, orbital assignments in 80: 8841x Alkyl halides 96: 180544u Alkyl hypochlorite gas-phase samples 95: 88644h Alkyl iodides 77: 61160p Alkyl isocyanides 86: 180276b Alkyl 81 : 97480q Alkyl radicals and alkyl nitrites 91 : 174602s Alkyl radicals and their precursor alkyl nitrites 101 : 38079z Alkyl styrenes 95: 79973n Alkyl sulfone, vinyl sulfone, aryl suI fones, alkyl sulfoimide, and sulfaryl halides 82: 148105b (Alkylthio)cyclopentanones 100: 34016h Alkyl vinyl ethers, conformation in relation to 87: 183858z Alkyl- and fluoroalkyl-substituted amines 86: 105721q Alkyl-substituted radical cations 92: 137965n Alkylamines and aliph. alcs., sum rule in 80: 47039m Alkylbenzenes 91 : 140000d Alkylcadmiums and cadmiums 88: 67589j Alkylhalobenzenes 103: 104466t Alkylidenenorbornadienes 103: 104408a Alkylmercury chlorides 95: 21946ge Alkylphenylcyclopropenes 101 : 229568t Alkylpiperidines 96: 103485y Alkylsilyl 87: 133520n Alkyltin cmpds. 89: 23320f iron cluster complexes 98: 107487q 89: 59355k Alkynes, uv 83: 105956h Alkynylmercury(II) cmpds. 100: 192009n Alkynyltin cmpds., a-n interactions in 102 : 79011 k Allene 88: 88700d Allene and 100 : 190994f 5

Allene methyl substituted derivs. 80: 42678j Allene, angular distribution of, asymmetry parameters 88: 120158w Allene, deuterioallene, and tetrafluoroallene 81 : 119429j Allenes and acetylenic allenes 83: 178061x Allenes, electronic struct. in reI. to anal of 87: 200620k Allenyl anion 98: 197502t Alloxazine and isoalloxazine 92: 119200e Allyl and benzyl radicals 89: 107100x Allyl 100: 156743p Allyl halides 81 : 8152u Allyl halides and vinyl halides 79: 110101x Allyl iron complexes 96: 218006k Allyl methyl & methyl sulfide, carbon- bonding in relation to 77: 95168n Allyl , hyperconjugation in relation to 78: 110334e Allylic alcs. and ethers of rigid geometry, conformational effect on 89: 214727d Allylic anions & deuterated derivs. 102 : 14491x Allylic ethers and alcs. 91 : 149062h Allylic radicals formed in gas-surface rxns. of alkenes over oxide 99: 121628p Allylmercuric chloride, hyperconjugation in reI. to 79: 59795x Allylmercury cmpds., conjugation in relation to 93: 185272b Allylruthenium complex conformers 96: 34352p Alternating vinylcarbazole 99: 23267a Aluminum 78: 90783v Aluminum monofluoride and aluminum trifluoride 101 : 160614k , 5f electron localization in rel. to 101 : 14431g Americium, nature of shakedown satellite in 101 : 180466s Amides, ureas, and their thio analogs, correlatn. of 82: 15466ge Amidogen radical 93: 57608d Amine- trifluoride complexes 78: 117376d Amines 100: 147981u Amines and amides, protonation in relation to 87: 67721a Amino acids 90: 168954w Amino acids 84: 165176j Amino acids and peptides 81 : 46604a Amino acids and their Me esters, gas phase structure 90: 55262a Amino acids and ureas 80: 132346d Amino- and (dimethylamino)cyclopentanol isomers, bond in relation to 84: 179135g Amino-substituted dioxaphosphorinanes 101 : 151959z Aminobenzoic acids and their metal chelates 86: 71660b Aminocyclopropenones and , MO calcns. 84: 163995b Aminodioxaphosphorinanes, cyclic phosphorodiamidates & phosphorodiamidothionates 100: 22699v Aminonorbornanol 89: 107671j Aminooxadiazoles 94: 207965e Aminophosphines and their complexes 94: 138913x Aminopyridines and cyanopyridines 81 : 161836q Aminothiophenol 98: 4195p Ammine chlorocobalt chloride isomers, shake-up satellites in 89: 171520m Ammine-, aqua-, and carbonylpentacyanoferrates 91 : 133231b 6

Ammonia 94: 216956e 102 : 140263n Ammonia & ammoniumyl 102 : 228895f Ammonia and ammonia-d3 97: 30638j Ammonia and nitric oXlde, 3-photon resonant 4-photon ionization processes in 98: 206985g Ammonia cation, second band in 99: 166030d ". Ammonia, carbon oxides & nitrogen oxides 76: 52655f Ammonia, and , shakeup peak assign. in 92: 223866n Ammonia-synthesis catalysts 94: 72168z tetracyanoquinodimethanide 83: 199818q Amphetamine analogs, psychotomimetic activities 95: 180665p Amphetamines and phenethylamines, psychotomimetic act. 90: 114912n Angle-resolved of gas-phase mols. using synchrotron radiation source 99: 166445t Anilide, benzyl and phenylnitrene anions 101 : 191047g Aniline and its methyl-substituted derivs. 77: 158524y Aniline, autoionizing Rydberg structure in 103 : 203194j Aniline, gas-phase 102 : 175663v Aniline, nitrobenzene, or p-nitroaniline, hyper- polarizability in relation to 92: 197693g Aniline, phenol or 102 : 45183c Anilines and phenol derivs., steric hindrance in rei. to 78: 123810g Anilines and phenylphosphines 87: 84328v Anilines, toluidines, and phenylenediamines 91 : 74051t 118]Annulene, MO calcns. correlation with 96: 19013ge [4n]Annulenes 86: 42603e [ 10] Annulenes 100: 174124s and its dihalo deriv., MO shifts in anal. of 80: 76414k Anthracene , photon coincidence in 99: 130894z Anthracene, intermol. relax. energies in rei. to 88: 73775h Anthracene-pyromellitic dianhydride complex 85: 176437s 87: 4909x Anthracenes 102 : 45298u Anthracenes and arom. polymers 79: 17611 d fluoride, bismuth fluoride, and fluoride, valence band 84: 97560c Antimony tetraat. cmpds., in gas state 101 : 140458j Antimony trihalides 82: 148063m 88: 161314n Argon 76: 92783c Argon and , angular distribution of 89: 14432s Argon, from outer shell, correl. satellites in reI. to 90: 64096b Argon, and xenon,angular distr. from p-levels in 100 : 218424w Argon, satellite spectra of, Ci alcn. of inten. dist. in 96: 152020b Argon, satellite structure in 97: 46813y Argon- van der Waals complex 101 : 100711 e Argon-xenon van der Waals mol., using resonant- ly enhanced multiphoton ionization 103: 61932x Arom. heterocyclic cmpds. 88: 128722w Arom. hydrocarbons, MO assignment of 99: 174927s Arom. ketones, electrochem. activity in relation to 87: 191091j Arom. ketones, x-ray fluorescence in relation to 101 : 90256u 7

Arom. mono- and diketones 91 : 156878g Arom. olefins 95: 42098e Arom. sulfides and sulfones 87: 151205t Arom. sulfinylamines 97: 91542v Aromatic amines, MO calcns. in relation to 103: 87384v Aromatic heterocycles and hydrocarbons 82: 154955v Aromatic hydrocarbons 77: 74646b Aromatic hydrocarbons C18H12 77: 74402u Aromatic hydrocarbons ana their perfluoroanalogs 77: 27168n Arsabenzene and phosphabenzene, angular and energy dependence of band intensities in 86: 54571f Arsabenzene, phosphabenzene and stibabenzene 78: 104216b and its cmpds. 84: 97563f Arsenic cmpds. 76: 79110m Arsenic dimeric and tetrameric mols. 94 : 148039f -doped polyacetylene 93: 104370g Arsenic pentasulfide 92: 87256j Arsenic trihalides in vapor phase 85: 133692d Arsenic ylides 84: 163713h Arsenic, valence band structure from 97: 101206e Aryl- and thienylethylenes 96: 171675k Arylaziridines, substituent effects on 97: 91575h Arylcyclopropanes and related cmpds., study of electronic interactions by 88: 30049g Arylenebicyclobutanes 95: 167963q Arylmercury complexes 102 : 220969n Arylsilane and -disilane 94: 29680y Atoms 97: 136125e Atoms & mols. using synchrotron radiation source 96: 13370c Atoms using synchrotron radiation source 99: 130890v Atoms, correlation effects in 89: 171542v Azaanthracenes and -phenanthrenes 84: 16422j Azabenzenes 91 : 174338k Azabenzenes and azanaphthalenes 76: 92781a Azabenzenes and azanaphthalenes 76: 92795h Azabenzonorbornyl derivs., homoallylic interaction 86: 54812k Azabicyclo[3.3.1]nonane, its oxo derivs. and analogs 93: 113622t Azabicyclooctanes and bicyclooctanones, MO calcns. 95: 114282k Azabicyclotetradecene 98: 71898h Azaboranicyclooctane 84: 179066k Azaboratricycloundecanes 103: 160559n Azacycl[3.3.3]azines 103 : 22063v Azanaphthalene and azaanthracene oxides 83: 192063f Azanaphthalenes 76: 92796j Azanorbornenes 98: 197372a Azapor'phyr ins 81 : 179632e Azetine 100: 50955u Azidohalobenzenes, MO calcn. in relation to 86: 42672b Azidopyridine in relation to 97: 181530u Azines 100 : 191026d Azines 85: 45671r Azino group-contg. mols. 83: 50475t Aziridinenamines 96: 84933z Azo cmpds. 90: 86199q 8

Azo cmpds. 82: 148108e Azo cmpds. 84: 67563p trans-Azobenzene and benzalaniline 82: 138745w trans-Azobenzene, substituent effects on 93: 25648a Azobenzenes and model cmpds. 89: 179333y Azoluracils 95: 19914j Azulene and radical cations, Me sub. effects 87: 38668h Azulenes, Rydberg states in relation to 99: 113211 g Azulenophane isomers 94: 217064z d-Band metals, anomalous thermal effects in 100: 423775 80: 76427s Barium 83: 170615k Barium and 76: 160605y Barium and europium 76: 160605y Barium and 92: 119053j Barium atoms, autoionization in relation to 100: 129251v Barium cmpds., anomalous chern. shifts in 101 : 180513e Barium halides 90: 95008d Barium, europium, , and ytterbium 91 : 219928w Barium, quantum-defect theory in relation to 99: 13442q Barrelenes and benzobarrelenes 98: 71331 t Benzamides 89: 41726x and bromobenzene , MO-band in reI. to 79: 145538x Benzene and hexadiyne isomers 89: 179077t Benzene and hexafluorobenzene, angle-resolved 98: 98328j Benzene and monohalobenzenes, angular dist. in 90: 38203q Benzene chioro derivs. 89: 188637c Benzene derivs. 89: 41727y Benzene derivs. 83: 77891n Benzene derivs., effect of intramol charge transfer on 96: 34373w Benzene fluoro and methyl derivs. 77: 68330c Benzene in gas and solid phase, Penning ionizatn. spectra in relation to 96: 60405c Benzene substituted derivs. 83: 170608k Benzene vapors 78: 50324q Benzene, MO calcn. and assignment in 86: 43046n Benzene, Multiphoton ionization study by 101 : 14436n Benzene, two-photon 88: 88692c Benzenethiol, p-state assignment in relation to 96: 171644z Benzimidazole, benzothiazole, benzoxazole and benzoselenazole 90: 86507p Benzo-substituted bicyclic and tricyclic alkenes 89: 4216ge Benzo-substituted thiocarbonyl heterocycles 83: 146678n Benzo[b]selenophene and benzo[b]tellurophene 84: 179051b Benzobicyclooctadienes 96: 5808m Benzocycioalkanes, MO calcns. in relation to 78: 146977f Benzocyclobutadiene 91 : 219926u Benzohorbornadienecarbonitrile 91 : 192705g Benzoic acid and its derivs. 94: 93173n 86: 88726a Benzonitrile and ethynylbenzene and its derivs., uv 81 : 161838s Benzonitrile and its derivs. 90: 5460t and benzene, screened INDO model for assign. in 85: 114350z 9

Benzonitriles, substituent effects on 103: 141359f Benzonorbornadienes 89: 196863p Benzoquinone and dithiobenzoQuinone 98: 71347c Benzoquinone methide 89: 214533n p-BenzoQuinone and methylated p-benzoQuinone 84: 42687u p-BenzoQuinone, MO parameters in reI. to 94: 111668j Benzoquinone, SCF-Xa-scattered-wave calcns. of 97: 203464e 1,4-BenzoQuinones, carbonyl effects in 86: 197496w Benzosilacycloalkenes 94: 29681z Benzothiazoles, substituent effects on 83: 8915m Benzothiete and benzothiete 93: 46474f Benzothiophenes 91 : 38352h 1-Benzothiopyran and its related cmpds. 85: 114323t Benzotris[c]furazan oxide 77: 12093k Benzoxadiazole 91 : 192304a Benzoyl chloride 90: 167483e Benzoyl halides 102 : 78203n Benzvalene, MO in reI. to 86: 105325p Benzyl halides, carbon- hyperconjugation 79: 31115b Benzylideneaniline 81 : 104507 j Benzylidenetrimethylphosphorane 83: 177577h Benzyl imidazol ines 91 : 168668b Benzylmanganese pentacarbonyl 103: 22727Q Benzylmercuric chloride, vapor phase conformatn. detn. by 83: 163215b 89: 171495g Beryllium cmpds. 89: 171318b Beryllium cmpds. 94: 92983Q Beryllium fluoride 98: 116237k Bery 11 ium ox ide 79: 98692f Beryllocene 91 : 38706b Bicarboxylic acid, MO and conformation in relation to 87: 67479c Bicyclic alkenes, reactivity with nitrenes in relation to 103: 141176u Bicyclic amines and diamines 95: 168268d Bicyclic azo oxides 86: 88551Q Bicyclic diketones 87: 38308r Bicyclic endoperoxides 90: 186430b Bicyclic peroxides 93: 57613b Bicyclic cmpds., ab initio MO calcns. 89: 107584h Bicyclic unsatd. alcs., hydrogen bond in relation to 87: 183828q Bicyclo[2.1.0]pent-2-ene 92: 17209ge Bicyclo[3.2.2]nonane and olefinic derivs. 78: 97011 a Bicyclobutane 98: 215052c Bicyclohexane 100: 164837n Bicyclohexanetriones 96: 180843r Bicyclohexylidene 103: 169219j Bicyclononatrienone 82: 42752v Bicyclooctadiene, bicyclooctene, and bicyclooctane 86: 88634u Bicyclooctane derivs. 88: 135965f Bicyclopentanone 102 : 5363e Bicyclopropenyl 97: 91305v Bicyclopropy 1 85: 12127Q Bicyclopropyls 97: 54914x Biferrocenylene and biferrocene 99: 104640u Binary and ternary chlorides 101 : 81116w 10

Binuclear rhodium complexes with phosphate 95: 107697w BioI. mols. and dicarbonyls 88: 30063g BioI. 89: 5587u Biphenyl 103 : 122853w Biphenyl derivs. and related cations, absorption spectra in" relation to 99: 166202m Biphenyls, MO in relation to 84: 8943ge Bipyridine and its disubstituted derivs. 98: 188486p Bipyridines 103: 214279s Bipyridines and their mono-N-oxides 95: 131834j Bipyrimidines 97: 91534u Bipyrryls, conformational anal. by 90: 151907k Bis(n-allyl), correlation effects in 103: 223779g Bis(n-allyl)nickel, valence ionization energies ab initio Green's function method calcns .... 103: 160679b Bis(1,1-diethyl-3-thiobenzoylthioureato)nickel 96: 27714e Bis(arene)metal complexes 99: 105419r trans-Bis(bindonylene) 76: 51580r Bis(cyclooctatetraene)actinide complexes 86: 120564j Bis(cyclopentadienyldicarbonylchromium, - and -) 101 : 111112m Bis(dialkylamino)acetylenes and of tetrakis(dioalkylamino)allenes 101 : 129986j Bis(dimethylamino)cyclopropenone and related cmpds., MO interpretation of 81 : 19013a Bis(dimethylamino)dibenzoheptafulvene radical cation 101 : 17061ge Bis(dimethylamino)fluorene and related cmpds. 10 1 : 210108w Bis(ethyliminopentanedioneoximato) 87: 93870t Bis(pentadienyl)iron 96: 199850n 1,2-Bis(pentafluorophenylthio)ethane 95: 72354c Bis(pentamethylcyclopentadienyl) dichloride 93: 158595c Bis(tri-tert-butylphenyl)diphosphene 97: 216322g Bis(tri-tert-butylphenyl)diphosphene 99: 202946t Bis(trimethylsilyl)amide of metals 86: 24192r Bis(triphenylphosphine)iminium salts 77: 81524p Bis-(n-allyl)nickel and its methyl-substituted derivs. 86: 4430p Bis[carbonyl(cyclopentadienyl)nickel] 98: 54174b Bisallylic oxygen cmpds. 85: 45689c Biscycloalkenobenzenes and naphthocyclobutenes 89: 107657j Bismethanoparacyclophane and paracyclophane, through-bond interaction in relation to 97: 38352g Bismuth and lead 95: 212355f Bismuth trihalides, relativistic interpretation of 98: 43629c Bismuth triiodide and lead diiodide 87: 209215q Bisstannyl and bissilyl alkanes 83: 77978w Bithienyls and dibromobithienyls 86: 170711a Borane adducts 102 : 140213w and carboranes 88: 97137c Boranes and tetramethylethylene 82: 138775f Boratranes 99: 195043r Borazines 76: 152733y Boron 5-membered heterocycles 84: 37136j Boron 82: 160458b Boron hydride sulfide 80: 8857g 11

Boron 83: 123789k Boron hydrides and carboranes in vapor state 78: 50339y , angular distribution and branching ratio in 101: 180501z Boron trifluoride, mutimode John-Teller and pseudo-Jahn-Teller effect in boron trifluoride monopos. in reI. to 98: 115936a Boron trifluoride, using synchrotron radiation 101: 200784z Boron trifluoride, vibrational fine structure in 96: 77105c Boron trihalides and halo-dimethylamino boranes 80: 42672c Bridged [14]annulenes and dicyclohepta[cd,gh]pentalene 82: 57335k Bromamine 88: 161152h and atoms 89: 188656h Bromine and iodine 76: 66112p Bromine monochloride 88: 14046y Bromine, krypton and bromides 3d orbitals, mol. effects on angular distribution parameter from 96: 225978g Bromine-trialkylamine cmpds. 85: 39092m Bromo- and iodithiophenes 88: 30048f Bromo- and iodomethanes 82: 131750k Bromo- and iodotrifluoromethane 88: 73786n Bromobenzene and dibromobenzenes 88: 128718z Bromoethylenes and bromopropene 77: 146029c Bromonortricyclene 102: 86961y Butadiene cation 101 : 151226h Butadiene derivs. 78: 3391z Butadiene-, cyclobutadiene- and cyclooctatetraeneruthenium tricarbonyl 98: 25104y Butanetetrones 103 : 37051p Butatriene and its derivs., MO calcn. of 88: 61723b Butatrienehexacarbonyldiiron complexes 97: 163202j Butatrienes 81 : 24580n Butene isomers 84: 134783a tert-Butoxynorbornadiene 83: 192424z Butyl- and (naphthylbutyl)naphthalene 79: 125392s tert-Butylacetylene derivs. 95: 15643x tert-Butylallenes 102: 148594s Butylbenzene isomers 91 : 46956y tert-Butylbenzenes 103 : 214610t sec-Butyllithium and isopropyllithium, gas phase 101 : 191991k C and N-methylmethylenimine 90: 103730a C16-Hexaquinacene 90: 54333n C20 and C2HO anions 99: 212031e and dihallde valence bands 98: 152262y Cadmium and zinc halides, ligand fields splittings and intensity variations in 98: 188500p , band structure from 98: 98318f Cadmium halides and zinc halides in gaseous state 80: 42677h Cadmium vapor, initial state config.-interactn. satell. 81 : 161843q Caged phosphorus cmpds. and related acyclic species 86: 148439w 83: 199630x Carbazole N-substituted derivs. 99: 130733w Carbazole and alkylcarbazole radical cations 103: 186288y Carbazole derivs., 100 : 147963h Carbazoles 102 : 5526k 12

Carbodiimines and sulfurdiimines 86: 197487u Carbon chalcogenides 80: 76418q 77: 146053f Carbon dioxide 89: 223375q Carbon dioxide 102: 35942k Carbon dioxide 99: 113361£ Carbon dioxide 98: 80963c Carbon dioxide and , spin polarizatn. in 92: 172103b Carbon dioxide excited with po~arized radiation 100 : 200354p Carbon dioxide monocatio~ in B Eg+state 100 : 218425x Carbon dioxide monopos. ion 87: 175417q Carbon dioxide, angular distributions of 100: 218466m Carbon dioxide, autoionizing resonances in synchrotron radiation-induced 97: 136107a Carbon dioxide, differential and total ionization cross sections for 97: 171867v Carbon dioxide, , and 93: 212836x Carbon dioxide, photoionization branching ratio paradox in relation to 100: 164831f Carbon dioxide, shape resonance in 101 : 160630n Carbon dioxide, vibrational assignment of cation from high-resoln. angle-resolved 101 : 100690x Carbon dioxides 86: 10474x 81 : 70804m 78: 142236r Carbon disulfide 92: 155585t Carbon disulfide and carbonyl sulfide 88: 113051 c Carbon disulfide and carbonyl sulfide, angle-resolved 97: 136133f Carbon disulfide, angle-resolved, excited with polarized resonance radiation 100: 200355q Carbon disulfide, inelastic scattering and satellite fine structure effects in 101 : 200732f 77: 12089p Carbon monosulfide 80: 42670a Carbon monosulfide, satellite lines in 86: 24204w 82: 9756b Carbon monoxide and nitrogen 82: 148075s Carbon monoxide and nitrogen 85: 54304a Carbon monoxide cation 95: 212556x Carbon monoxide cation and nitrogen mol. cation 86: 130684n Carbon monoxide, comparison with auto ionizatn. spectra 99: 221700z Carbon monoxide, inner-valence-shell, electron correlation and shaperesonance in relation to 99: 166371r Carbon monoxide, resonantly enhanced four-photon ionization in relation to 99: 166437s 89: 82641j Carbon sulfide anion and nitrogen sulfide anion 97: 190757a and tetrachloride and tetrachloride, shape resonance-induced features in angular distribution parameter for 101 : 200731e Carbon tetrachloride and sulfur , shape resonances and partial cross sections 103: 19694k Carbon tetrachloride, angular dependence in 97: 226166y 13

Carbon tetrafluoride and , asymmetry parameters for 102 : 212165g and 103 : 223814q Carbon tetrafluoride, cross sections for angle-resolved 102 : 14531k Carbon tetra 101 : 100349t Carbon, aluminum, cobalt, and palladium, elastic photoelectron collision effects in 101 : 14439r and thiocarbonates 84: 73231v Carbonium ions, MO calcns. in relation to 86: 89019J Carbonothioyl(tetracarbonyl) iron 97: 46804w Carbonyl and nitrosyl , in trans. metal complexes 91 : 131714n Carbonyl compds. 101 : 72223b Carbonyl and carbonyl halides 76: 66107r Carbonyl cyclopentadienyl molybdenum and tungsten cmplxs. 87: 76108h Carbonyl & thiocarbonyl selenide & rel. cmpds. 83: 68756v Carbonyl sulfide 94: 39181a Carbonyl sulfide, autoionization in 94: 217066b Carbonyl sulfide, carbon dioxide and carbon disulfide vibronic coupling in relation to 98: 116459J Carbonyl sulfide, in autoionization process study 99: 30301k Carborane(12) isomers 96: 112881 b Carboxylic acids and esters, acidity & basicity 89: 146277e Carboxylic acids and related cmpds. 77: 100528m Carbyne polynuclear cobalt carbonyl clusters 96: 122994e Carcinogens 99: 65439p a-Carotene and chlorophyll a 89: 180200J Cation radicals, UV spectra in relation to 88: 128444g Cations of hexatrienes and heptatrienes 94: 64910v and indium and compds., screening in relation to 103: 61934z Cerium cmpds., model calcn. and limit of large degeneracy in relation to 98: 116453c Cerium cmpds., with synchrotron radiation source 98: 116402k Cerocene 103: 215457k Cesium and cesium chloride 93: 84558u Cesium and 76: 160609c Cesium halides 81 : 84120x Cesium iodide 78: 90780s Cesium iodide 76: 117383d Cesium oxide 79: 36272k Cesium, oxidn. in relation to 96: 225977f Chalcanthrenes, MO calcns. in relation to 100: 5413e Chloramine and dichloramine 88: 200596c Chloramine and 89: 33828s Chloramine and methylchloramine 89: 155208k Chloramine, MO calcn. of 91 : 201343s Chlorine fluoride 76: 92791d Chlorine monoxide radical 91 : 81321J Chlorine using synchrotron radiation, as function of photon energy 98: 80979n Chloro, bromo, methoxy, and Me complexes of triindenylthorium and - 98: 54081u Chloro- and dichlorodiacetylene cation 96: 171461n Chloroacetylene 98: 142822s 14

Chlorobenzene and dichlorobenzenes 94: 217050s Chlorobenzenes & chloropyridines, correlations of 79: 11781n Chloroethanes and -methanes 86: 71659h Chloroethanes, chloroacetaldehydes, and chloroacetyl chlorides 83: 57590k Chloroethylene, MO interpretation of 77: 146039f Chlorofluoro hydrocarbons 99: 61295r Chlorofluorobenzene cations 93: 122812g Chlorofluoroboranes, uv 84: 10729t Chlorofluoromethane 87: 175416p Chloroketenes 100: 33807e Chloromethanes, MO interpretation of 79: 59790s Chloromethanes, SCF Xa calcn. of 97: 82203h Chloromethanes, SCF Xa-scattered wave method in calcn. 96: 225971z Chloromethyl cmpd. 94: 83190b Chloromethyl radical 98: 2247025 Chloromethyl radicals 100: 51018c (Chloromethyl) derivs. 95: 10578e Chlorophenylbenzodiazepinones 84: 104851d Chloropyridines and picolines 90: 38383y Chlorothioborine 89: 1204025 Chromate and permanganate 17: 159502q 98: 80988q Chromium allyl cmpds. 95: 33086x Chromium and molybdenum tetracarboxylates, MO calcns. 91 : 149047g Chromium and tungsten carbonyl complexes substituted with amines 88: 143957v Chromium and tungsten carbonyls 81 : 179629j Chromium atoms 98: 9722t Chromium benzene carbonyl complexes 19: 77625w Chromium carbonyl 91 : 114997q Chromium carbonyl complexes with organophosphine and organosulfide ligands 88: 1287115 Chromium carbonyl deriv. complexes 87: 209198m Chromium cmpds. multiplet structure in 3p-shell 87: 46339s Chromium oxide trichloride 91: 96983a Chromium pentacarbonyl azole complexes 91 : 99332y Chromium pentacarbonyl complexes with dihydro-and tetrahydrothiophenes and their S-oxides 90: 103164u Chromium complex 100 : 210059k Chromium tetranitrosyl 92: 188842 Chromium thionitrosyl and nitrosyl piano-stool complexes 103 : 196196f Chromium trichloride oxide 90: 15588e Chromyl chloride, uv 83: 1395625 Chrysene Me derivs., carcinogenic activity in rei. to 96: 6021t Cinnamic acid and cinnamamide 99: 104652z Cis- and trans-l-phenyl-2-(4-pyridyl)cyclopropanes in gas phase 90: 167924z Cmpds. contg. allylic carbon-oxygen bond 91 : 19246k Cmpds. contg. bent and twisted double bonds, MO calcns 98: 711005 Cmpds. contg. phosphorus, nitrogen, and heteroatoms, lone-pair electron effects and 91: 5481v Cobalt and iron and nickel 98: 116414r 15

Cobalt and iron complexes with methylamino­ bis(difluorophosphine) 94: 129951f Cobalt and iron maleonitriledithiolate Schiff base complexes. 90: 196901v Cobalt and iron phosphine cmplxs. 94: 113163v Cobalt and rhodium cyclopentadienyl carbonyl complexes 101 : 211420d Cobalt and cmplxs. 89: 110995x Cobalt carbonyl complexes contg. ethenyl and methylidyne radicals 95: 10605m Cobalt carbonyl complexes with various ligands 98: 116468m Cobalt carbonyl-methylidyne complex, orientation of methylidyne fragment in relation to 91: 205239j Cobalt carbyne cluster 99: 105415f Cobalt complexes with acetylene derivs. 93: 228110m Cobalt coordination cmpds., internal stds. for detn. of chern. shifts in 88: 200613f Cobalt cyano-complexes 98: 43515g Cobalt molybdate in presence of magnesia 92: 15532h Cobalt monoxide 92: 101991d Cobalt substituted acetylacetonate complexes 90: 130190f Cobaltocene 96: 122989g Complex atoms 101 : 63034p Complexonates 96: 225624p Condensed arom. hydrocarbons, ionization potential from 88: 189396q Condensed ring arom. hydrocarbons 102 : 184606f Conjugated acetylenic aldehydes and ketones 91 : 192623d Conjugated ethylenic aldehydes and ketones 89: 196495v Conjugated phenylalkynes, electronic structure 90: 186111z Conjugatedenynes, substituent effects on 90: 185899z 8-Coordinate sulfur chelate complexes of molybdenum 98: 134415w 95: 123519q Copper 88: 91108u Copper 91 : 184561y Copper 92: 32141h Copper 93: 51635k Copper 18: 90522j Copper and copper contg. oxygen 92: 138262t Copper and nitrates 91 : 184551p Copper aqua dimethyldiimidazolylsulfide complex cation methylsulfate salt 100 : 184183v Copper atoms and clusters in rare gas matrix 95: 228821r Copper atoms, resonant satellite structure in 91: 153434x Copper carboxylates 84: 181256n Copper complexes with pyrazolylgallate & pyrazolylborate 83: 155182y Copper dihalides, satellite structure in 95: 15659g Copper diketone complexes 81 : 91499c Copper halide and chloride gas-trimers 89: 120406w Copper halide and silver halide trimers in vapor phase 92: 138260r Copper iodide 81 : 161846t Copper monochloride 92: 138248t Copper oxides 18: 11848a Copper sulfide 89: 91511k Copper vapor, two-electron satellites in 95: 212560u Copper-tetracyanoquinodimethan complexes 80: 69864d 16

Covalently bonded transient mols., ground-state vibrational levels from 103: 45024x Cross-conjugated polyenes 99: 139174x Crown ether-alkali fluoride cmplxs. 93: 203461u Cuprous bromide, temp. dependence of 86: 36129p Cuprous chloride, secondary electron spectra in reI. to 98: 206961w Cuprous fluoride and cupric fluoride 94: 55448y Cuprous halides and silver iodide 82: 49680d Cuprous oxide 81: 18227m Cuprous oxide 82: 79424r and related isoelectronic cmpds. 81: 70777e Cyanoalkene 84: 104874p Cyanodiacetylene and its alkyl derivs. 93: 149237k p-Cyano-N,N-dialkylaniline 103: 149914d and its cation 92: 49564a 83: 183809b Cyanogen azide and cyanogen isocyanate 87: 46331h Cyanogen cation and hydrocyanic acid cation 78: 22304q 86: 148457a Cyanogen 101: 219044e Cyanogen mol., shape-resonance effects in 99: 184484j Cyanogen mol.,triply differential 99: 149051u Cyanogen-hydrocyanic acid mixt. compn. in reI. to 97: 5542ge a-Cyanoisopropyl and benzyl radicals, ionization potentials by 87: 4843w Cyanomethyl- and cyano(trifluoromethyl) 86: 120191k Cyanoquanidine, core-electron ionizatn. energy in reI. to 96: 207837f Cyanoselenium chloride and bromide & dicyanide 95: 228782d Cyclazines and related cmpds. 88: 120419g Cyclic amines 80: 59107v Cyclic and linear silanes 87: 38352a Cyclic arom. ethers 84: 134744p Cyclic azo cmpds., conrg. cyclopropane rings 80: 81588z Cyclic azo oxides 86: 105209d Cyclic di- polyamines 82: 56986m Cyclic diketones, orbital sequence in relation to 93: 131899t Cyclic dimethylhydrazines, conformation in relation to 80: 145260w Cyclic ethers 78: 64928b Cyclic imide N-Ph derivs. 101: 10073 1m Cyclic oxamides, MO calcns. in relation to 94: 102299n Cyclic peroxylactones 99: 52923s Cyclic phosphites 92: 163429k Cyclic phosphorus esters 95: 24133h Cycloaliph. alcs., hydrogen bonding in relation to 87: 52589q Cycloalkanamines, and dehydroquinuclidine 85: 77410w Cycloalkanediones 80: 14145q 'Cycloalkanone enamines 87: 191766h Cycloalkenes and methylenecycloalkanes 87: 133642d Cycloalkylhydrazines contg. pyrazolidine, hexhydro pyridazine, and tetrahydropyridazine structures, conformational anal. by 82: 9777 j Cycloalkylideneselenoketenes & analogs 102: 166196t Cyclobutadiene and trimethylenemethane tricarbonyliron complexes 90: 203292c 17

Cyclobutadiene dimers 81 : 119689u Cyclobutadieneiron tricarbonyl complex, MO calcns. 99: 105455z Cyclobutane 81 : 104448r Cyclobutane derivs. contg. unsatd. chains 88: 189814z Cyclobutanedione and related systems,MO calcns. 91 : 140154g Cyclobutene-1,2-diones 89: 107602n Cyclobutenedione deriv. pyrolysis in relation to 94: 174024s Cyclobutenediones and benzoquinones 89: 107128n Cyclodecadiyne 103 : 141494w Cyclodecatetraene 90: 5454u Cyclododecatriyne 92: 5899j Cycloheptanaphthalene, cyclobutacenaphthalene, and methenophenalene, MO in relation to 91 : 81325p (Cycloheptatriene)tricarbonyliron complexes 99: 175982t Cyclohexadiene and related cycloalkenes 85: 133698k 1,4-Cyclohexadiene, angular distribution in 89: 214546u . Cyclohexane and halocyclohexanes 79: 145649j Cyclohexane and its halo derivs. 79: 136174y Cyclohexanones, conformation in relation to 86: 120647p Cyclohexenones and acetophenones, substituent effects on 97: 91539z Cyclooctadiene 92: 128172z Cyclooctadienynes 102 : 95156a 1,5-Cyclooctadiyne and 1,6-dithiacyclodeca-3,8-diyne 81 : 168764y Cyclooctatetraene and hydrogenated derivs. 78: 96756k Cyclooctatetraene dianion in THF soln. 97: 63621b Cyclooctatetraene, styrene and related cmpds. 89: 107023z Cyclooctatetraeneiron tricarbonyl 94: 29956t Cyclooctatetraenyl radical anion and perinaphthenyl anion, exptl. vs. theor. 91 : 38717f Cyclooctenyne 89: 196393k Cyclopentacyclazine 88: 120174y Cyclopentadiene and fulvene 77: 120461n Cyclopentadiene fused to bicyclic systems 92: 180579b Cyclopentadienethione and monothiobenzoquinone 95: 96371g Cyclopentadienone 87: 175399k Cyclopentadienone 89: 5580m Cyclopentadienyl complexes 82: 79122r Cyclopentadienyl complexes of titanium, zirconium and 100: 210044b (Cyclopentadienyl) (Cycloheptatrienyl)zirconium, -, and -molybdenum 83: 163204x Cyclopentadienyl lanthanides and 95: 114272g Cyclopentadienyl metal dinitrosyl halides 95: 105957g Cyclopentadienyl(dimethyldiboracyclohexadiene)cobalt 96: 123005v Cyclopentadienyliron carbonyl complex 93: 203493f Cyclopentadienyliron carbonyl complexes 93: 149224d Cyclopentadienylmanganese alkene carbonyl complexes 95: 202777f Cyclopentadienylmanganese carbonyl 86: 29091s Cyclopentadienylmercuric chloride 96: 199826j Cyclopentadienylnitrosylnickel cation 90: 130164a Cyclopentadienylrhodium with bridging carbonyl 98: 89635e Cyclopentadienyluranium and cmpds. 86: 88543p Cyclopentanone and oxacyclopentanone analogs 79: 31058k Cyclopentene and silacyclopentenes 85: 101841k 18

Cyclopentenes 88: 73966w Cyclopentenetrione and tropoquinones 97: 46844j Cyclopentyl and cyclohexyl radicals and pyrolysis prod. 95: 186398a Cyclophanes 93: 84527h Cyclophanes 101: 90263u [2.2]Cyclophanes 92: 206675g [2.2]Cyclophanes 95: 5980r Cyclophanetriene 79: 31055g Cyclopolyphosphines 89: 82630e Cyclopropane and cyclopropene derivs., subst. effects on 97: 215343c Cyclopropane, potential surface in rel. to 96: 216869v Cyclopropane,angle-resolved 103: 203174c Cyclopropanol or allyl alc. 100: 138426h Cyclopropanones 88: 5745y Cyclopropene Ph derivs. 101: 160616n Cyclopropenone 80: 126569n 86: 188717s Cyclopropyl conjugated 1,2-diketones 81: 36885d Cyclopropyl derivs. of norbornane & related cmpds. 84: 89014n Cyclopropylallenes 85: 76958u Cyclopropylbenzenes 96: 198931c Cyclopropylbutadienes & spiroheptadiene 102: 184595b Cytochrome c 89: 210716b Cytosines 89: 23328q Decacarbonyldihydridotriosmium 97: 101175u Decahydrotrimethanoanthracenes, n-orbital interactn. in 99: 175100d Decamethylferrocene, and decamethylferrocene-bis(tetracyano- p-quinodimethan) complex 87: 133353k Dehydroalanine cyclic dipeptide 103: 71696n Dehydrotropylidene, dehydrooxepin and fulvenallene 91: 149082q Deuterated 90: 167454w Di- and tetrahydrothiophene, hyperconjugation in reI. to 79: 65572p Di-Me cadmium and related cmpds in gas phase 88: 179867e Di-Me diselenide 86: 138920g Di-Me ether- heterodimer in gas phase 92: 85536b Di-Me or di-Et ethers, total photoion yield in rel. to 88: 21682f Di-Me sulfide 98: 116410m Di-Ph 97: 126686z Di-tert-adamantyl disulfide 92: 128241w Di-tert-butylcyclopentadienone isomers, inductive effect of carbonyl group on 80: 59104s Di-tert-butylcyclopropenone and trans-2,3-di-tert- butylcyclopropenone 81 : 49087v Di-tert-butylpolyacetylenes 90: 38173e Di-tert-buylthiophene dioxide 80: 59106u Diacetylbis(methylimine) 84: 154685g Diacetylene polymers 103: 196475w Diademane analogs 80: 2910x Dialkoxyazoxybenzenes 96: 19485r 1,4-Dialkyl 1,3-butadiynes 87: 133329g Dialkyl(phenylthio)boranes 87: 167018v Dialkyl-substituted alkenes, MO calcn. of 88: 120429k Dialkylamido complexes 92: 119223q (Dialkylamino)diazaphospholanes and related cmpds. 91 : 210466m 19

Dialkylaminovinylpyridines, dialkylaminostyrenes, vinylpyridines 102: 122468d Dialkylmercury cmpds. 85: 122813t Dialkyltin pentacarbonylchromium and -tetracarbonyiron complexes 19: 151289h Diaminodifluorophosphorane .·85 : 136450j Diarsines and diphosphines, in conformation study 80: 139234z Diaryl dichalcogenides 95: 42163x Diat. halides, charge dist. in relation to 102 : 115645r Diat. mols., nuclear motion effects in 99: 166446u Diazaadamantane derivs. 86: 188601f Diazaadamantanone 82: 91494t Diazabasketene, diazadeltacyclene and related cmpds. 85: 77010r Diazabenzene oxides 83: 192062e Diazaboroline and diazaborolidine derivs., electron delocalization in relation to 81 : 62596e Diazacyclophanes 96: 34361x Diazadioxathiapentalene & selenium and analogs 93: 1121a Diazafluorenone 96: 54319c Diazanaphthalenes 16: 119668h Diazanaphthalenes and their fluoro derivs., uv 83: 105955g Diazanaphthalenes and their polyfluoro derivs. 80: 2911e Diazene 82: 138116n Diazene and dihydrodiazene, vibrational structure in 81: 93208h Diazene and methyldiazene 85: 54311a Diaziridines . 19: 145831u Diazoalkanes, orbital sequence in relation to 80: 26455d Diazocyclopentadiene, electronic structure in relation to 81 : 119341f a-Diazoketones 92: 138259x Dibenz[b,f]azepine analogs 91 : 56188p Dibenzo-p-quinodimethane 86: 29092t Dibenzocycloheptene analogs 85: 93681r Dibenzophosphorin and dibenzarsenin 18: 15138k Dibenzotetrathiafulvalene 84: 82051v Diboron tetrachloride and tetrafluoride, SCF MO calcns. 18: 22283g Dibromoalkanes and bromofluroalkanes, ionizatn. pots. 83: 192434c trans-1,2-Dibromocyclohexane, interaction of bromine lone pair orbitals in relation to 86: 42961v Dibromoethane conformers 89: 23660s trans-Dibromoethylene, uv spectrum relatnshp. with 86: 10481 x Dibromomethanes 82: 85590h Dibromotetracarbonyliron, Green's function in calcn. of 98: 80976j Dicarbaboranes 83: 105920s Dicarbapentaborane and its dimer and trimer 93: 94601y Dicarbonyl(cyclopentadienyl)manganacumulenes 99: 115965q Dicarbonyldicyclopentadienyltitanium 91 : 114353m Dicarboxylic acids and phosphorus cmpds. 92: 191411p Dicarboxylic acids and their derivs. 94: 200352u Dicarboxylic acids, phosphites and phosphates 92: 214431w Dichloroctimethyl , difluorodimethyl germane and di-Me-germane 91 : 1845752 Dichlorodithiabicyclooctane, conformation in reI. to 98: 197264s Dichloroethane 90: 161851y Dichlorofluoromethane in argon matrix 86: 139034h 20

Dichloroketene 93: 113419g Dichloromethyl Me ether 93: 167481q Dichloromethyl and dichloromethyl-d radicals 99: 203013y Dichlorophosphine 99: 53895w Dichloro~ilanediylene 102 : 142249m Dichromium and dimolybdenumcarboxylate complexes, elec- tronic struct. & metal-metal bond lengths in reI. to 99: 184443v Dicoronylene 103: 159852w Dicyanodiacetylene 91 : 201525c Dicyanogen 88: 112816u Dicyclopentadienyl lanthanide chloride bipyridine cmpxs. 101 : 171417z Diethoxybis(trifluoromethyl)allene and related cmpds. 99: 139197g Diethyl 2,3-bis(diethylamino)-1,3- cyclopentadiened icarboxy late 80: 26446b Diethynylnaphthalene and cyclic analogs of diethynylbiphenyl 95: 167930b Difluoramine 93: 84556s Difluoramine 93: 84557t Difluoro(difluorophosphinoamino)borane 85: 13216e Difluoroallene 90: 21791g Difluorobenzene 86: 113402b Difluorobenzene 87: 101534d Difluoroborane 95: 178300x Difluorodisulfane and thiothionyl fluoride 79: 36913v Difluoroethene isomers 93: 302525t Difluoroethylenes 90: 1675211" Difluoroisoselenocyanatophosphine 88: 130127z Difluoromethylene and 82: 111164u Difluorophosphine and its derivs. 77: 41154m (Difluorophosphino)amines 83: 70833m Dihalo cmpds. 77: 146043c Dihalobenzenes, neg.-ion state energies in reI. to 101 : 229826a Dihaloboranes 95: 54012k Dihalodiacetylene 90: 102895w Dihalodiacetylene, halodiacetylenes, and halomethyldiacetylenes 81 : 161859z Dihaloethane 83: 27089m Dihalonorbornanes 103: 122856z 2,5-Dihydrofuran derivs. 90: 186222k Dihydropyridines 80: 81561k Dihydropyrroledione and related cmpds. 100: 120341s Diimines and imines, MO calcns. for 98: 62630n Diiron ferraboranes 95: 141458d Diketonate complexes of and rhodium with carbonyls or ole fins 93: 195009k Diketones 81 : 77051x Dimeric chromium and molybdenum allyl complexes 94: 14686f Dimethanoanthracene and dimethanomaphthacene derivs. 88: 151855a Dimethanonaphthalene 95: 114574g Dimethoxymethane 95: 114588q Dimethoxynaphthalenes laterally fused to bridged bicyclic systems, stereoselectivity of singlet mol. oxygen addns in relation to 94: 3661t 21

Dimethyl and ethylene carbonates, oxalic acid, and dimethyl and diethyl oxalates 84: 120110n (Dimethylaminoalkyl)nitrobenzene, charge-transfer interaction in relation to 88: 50016s Dimethylaniline and dimethylphenylphosphine 11: 163101h Dimethylazabicyclooctyl system 91: 144094j Dimethylcyclopropane and polyalkylcyclopropenes 96: 6011q Dimethyldihydropyrene 16: 152148g Dimethyldimethylenecyclobutene and its dimer 99: 5033s Dimethylenebicycloalkenes 93: 185826k Dimethylenecyclobutanes 90: 54288b Dimethylenecyclobutene and its cyclopropanation prod. 92: 15461j Dimethylgermanone 102 : 185197k Dimethylgermathione and dimethylsilathione 99: 122572c Dimethylhexadiene isomers 101 : 54386c Dimethylhexahydropyridazine, variable temp. 93: 238700y Dimethylhydrazine 78: 51937d Dimethylhydrazine, dimethyl disulfide & dimethyl 83: 170620h Dimethylisoindene radical cation 93: 104379s Dimethylnitramine and dimethylnitrosamine 83: 113172q Dimethylnitrosamine 84: 29974r Dimethyloxabicycloheptatriene 103: 214304w Dimethyloxadiazolinones 90: 5681r Dimethylphenothiasilin, -germin, and -stannin and dimethylthioxanthene 87: 52302r Dimethyl(phenyl)triazolinethione and N-isopropylideneaniline 88: 88859n (Dimethylphosphino)- and (dimethylamino)benzenes 90: 86520n Dimethylquinodimethan, non-Koopmans theorem effecs. in 87: 22118t Dimethylsilacyclobutane pyrolysis products 94: 138807r Dimethylsilaethylene 97: 46798x Dimethylsilane, -, and -germane 101 : 211311a Dimethylsulfide and DMSO 102 : 94945m Dimethyltetracyclooctanedione, through-bond inter- action in relation to 99: 37904t Dimethyltetrahydrotetrazine and teraalkyltetrazenes MO calcn. of 83: 146647b Dimethylzinc 87: 175403g Dimolybdenum and dichromium tetraformates 90: 46348f Dimolybdenum formate 86: 162879w Dimolybdenum tetracarboxylates 86: 36669q Dimolybdenum tetraformates, MO study of 89: 120398v Dinitroanisole 101 : 110175x Dinitrogen difluoride isomers 87: 175411h Dinitrogen tetraoxide 86: 24213y Dinitrogen tetraoxide and nitrosomethane, shake-up satellites in 98: 80g62b 88: 97099s Dinitrogen tetroxide 86: 163310r Dinitrogen tetroxide 91 : 81337u Dioxa- and dioxadithiadecalins 99: 5023p Dioxacycloheptene and related cmpds. 97: 144187s ,Dioxygenyl ion, competition between autoionization and pre-dissocn. in relation to 102 : 228914m 22

Dioxygenyl ion, predissocn. inrelation to 102 : 175176p Dipeptides contg. 102 : 35957u Diphenyl sulfide methyl derivs. 83: 192441c Diphenylbutadiyne and diphenylbutenyne 93: 238023e Diphenylcarbodiimide 103: 36862s Diphenylcyclopropane and diphenyloxirane, oxidn. potentials in relation to 91 : 174655m Diphenylcyclopropene and its derivs., conjugative & inductive interactions in relation to 90: 54088m Diphenyldiphosphenes 101 : 111020e Diphenylpolyenes 84: 128485p Diphosphene 100: 6654w Diphosphenes, phosphorus double bond in relation to 99: 38545p Diphosphenes, phosphorus double bond in relation to 99: 38545p Diphosphine disulfides 94 : 173816q Diphthalocyaninato-actinide and -lanthanide complexes, satellite structures· in 90: 130165b Diphthalocyaninatothorium and -uranium 85: 151535j Dipyridylethylenes 87: 183618w Dirhodium tetracarboxylate complexes and their cations electron configuration in reI. to 98: 206610f Disilaasnthracene deriv. and dimethyldiphenylsilane 92: 110138h Disilane 87: 208743y Disiloxanes 97: 6391c Disilylaminodifluorophosphine and bis(diflu9rOphosphino)­ silylamine 91 : 150498m Dithiin and related cmpds. 92: 67351h DithiocarbazateMe esters and bis(Me dimethyl­ dithiocarbazato)nickel 94: 102571v Dithiolane 94: 46325d Dithiolane and tetrathiaspirononane, sulfur 3p AO interactions in relation to 86: 54835v 1,3-Dithiolethione and its benzo deriv. 84: 89070c Dithiolethione and its selenium analogs 86: 197478s Dithiolethiones, substituent effects on 82: 169588b (Dithiolylidene)carbonyl cmpds. and trithiapentalenes 76: 98615w Dithiooxamides and monothiooxamides 96: 67933g Dithiospirocycloalkanes and their ruthenium complexes 98: 134687m Ditungsten tetrakis(trifluoroacetate) 97: 171849r Dodeca fl uo ro tr icyc loundeca tr iene and tet radecafl uo ro tricyclododecatriene, chg. distn. in reI. to 77: 146025y Duihydrotriquinacene and tetrahydrocyclopentazulene 82: 169632m Duroquinone and isoelectronic boron fluoride analog 94: 46438t Edge-bridge decacarbonyltriosmium cluster in gas phase 100: 14812m Electron rich iron cyclopentadienyl arene complexes 98: 72373v Electron rich pentamethylcyclopentadienylphosphine cobalt complexes 99: 212670n f-Element coordination cmpds. 89: 206988z Enamines 96: 121851u Enolate neg. ions and alkoxides 97: 226464u Enzymes, in vacuum-UV region 97: 2882r Ephedrine, electron config. and sympathomimetic act. 96: 85809a Et radical 100: 208999y Et radical 87: 101533c 23

Ethane 81: 62713r Ethane 82: 138774e Ethane chlorofluoroderivs., uv 82: 148058p Ethane fluoro derivs. 81: 83838a Ethane radical cation 76: 105687b Ethane, MO calcns. in relation to 88: 135997t- Ethanediol and propanediole and in gaseous and liq. phases 102: 69703y Ethanediol in gas and liq. phases 90: 31621r Ethanediol in gas and liquid phases 91: 184581y Ethanediol, comparison of gas- and liq.-phase 92: 49843r Ethers 100: 67711 j Ethers and thio ethers 81: 104085v Ethylene 102: 87000w Ethylene 93: 149574t Ethylene and its deuterated derivs., 91: 156879h Ethylene and silyl derivs. 81: 12913k Ethylene and water isotopic species 94: 74240r Ethylene and propylene carbonate 82: 118025h Ethylene derivs. 79: 145554z Ethylene derivs. 89: 14445y Ethylene deuterated mols., Franck-Condon factor in relation to intensity in 102: 14227r , conformation in relation to 93: 7093m Ethylene halo derivs. 77: 68321a 86: 120314c Ethylene oxide and 83: 27218c Ethylene polymers 76: 127577t Ethylene radical cation and its deuterated derivs., vibrational struct. in excited states from 102: 122478g Ethylene sulfide 79: 85368e Ethylene trithiocarbonate and dithiocarbonate, electron structure in relation to 83: 146684m Ethylene, angle-resolved 97: 71828q Ethylene, angular distn. of photoelectrons in 77: 158515w Ethylene, multimode effects in 97: 153178s Ethylene, vibronic coupling effects in 90: 71318d Ethylenebis(acetylacetonimine) metal complexes 80: 139218x Ethylenebis(benzoylacetoniminato)cobalt and its adducts with nitric oxide and oxygen 78: 22287m Ethylenebisacetylacetoneiminatocobalt 83: 123359v Ethylenecarbonate and related cmpds. 87: 4908w Ethylenediaminetetraacetic acid derivs. 80: 81606d Ethylenic, benzenoid, and styrylpyridine systems, substituent effects on 83: 192314p Ethylidenenorbornene and vinylnorbornene isomers reactivity in relation to 103: 214760s Ethylthionacetate, methyldithioacetate and methyl thiolacetate 83: 50479x Ethyne 103: 36845p Europium, europium monoxide, and 92: 155601v Ferraboranes 88: 97138d Ferracyclopentadienyl derivs. 102: 149464m Ferrocene 88: 189466n 24

Ferrocene cmpds. 76: 52657h Ferrocenophane and its 7-oxa deriv. 103: 95519h Five-membered heterocycles 87: 38311m Fluorene and heterocyclic analogs 89: 196504x Fluorescence in coincidence with, of benzene fluoro deriv. cations 102 : 86918q Fluorides 76: 119659f Fluorides 77: 158518z Fluorides 78: 166748k Fluorinated Ph cmpds., perfluoro effect in 91 : 184574y Fluorinated acetylenes 87: 183648f Fluorinated bromo- and chlorobenzenes 93: 104377q Fluorinated diazabenzenes 81 : 36890b Fluorinated org. cmpds. 103 : 112682a and fluoroderivs. of acetylene and diacetylene 93: 104383p Fluorine., in , and 78: 130357t Fluoro- and tetrafluoromethane, MO calcns. in reI. to 90: 5683t Fluorobenzenes, ethylene and tetrafluoroethylene 86: 139207s Fluorobenzenes, fluoro group effect on 102 : 203537c anesthetics 96: 24731x Fluorocyclotriphosphazenes 93: 57603y Fluoroethers 83: 8637x Fluoroimidogen, ionization potential in relation to 97: 169252x Fluoromethanes and rare gas fluorides 99: 79495r Fluoromethanes, monopole shakeup and satellite structure in 103: 70870c Fluoromethyl cation 100: 191224s Fluoromethylidyne 100: 111611c (Fluoromethylidyne)phosphine and methylidyne phosphine, Green's function study of 99: 221699f Fluorophenols in gas phase 93: 16405s Fluorophosphaethyne 88: 105486h Fluoropyridines, ESR of radical cation analogs in reI. 100: 191009a Fluorothioborane mono-, di-, and trimer 101 : 142845g Fluorothiocyanate 97: 14415d Fluorotrihalomethanes 83: 27088k 76: 52052g Formaldehyde and its perdeuterio deriv. 96: 51644c Formaldehyde and , angle-resolved 101 : 200783y Formaldoxime and nitrosomethane 97: 101173s Formate and acetate esters 87: 200283c Formic acid and formic acid dimer in gas phase 98: 116444a Formic and related aliph. anhydrides 90: 102896x Formic anhydride 91 : 46960v Formyl fluoride 85: 4736x Formyl radical 93: 25437f Free and coordinated aminophosphines and related cmpds. 96: 60376u Fulvenallene, MO calcn. in rela~ion to 88: 169224d Fulveneketene, oxocyclohexadienylketene, fulvene-thio ketene and thiobenzopropiolactone, MO in relation to 90: 203056d Fumaronitrile and maleonitrile 77: 4487b Furan 93: 185535q Furan and butynone 93: 238043m 25

Furan and thiophene derivs. 98: 206965a Furan, pyrrole and thiophene MO calcn. in relation to 97: 38345g Furans, thiophenes, selenophenes, and tellurophenes, sUbstituent effect on 84: 104632h Furylarylethane derivs. 99: 96332c Fused cyclohexanediones, through-bond inter- action in relation to 102 : 184605e Fused ring arom. , MO calcn. of 92: 128192f Gadolinium, energy band structure from 99: 79539h Gadolinium, and their metal-rich chlorides 97: 82242v vapor 87: 60322n Gas anal. 90: 96950s Gas-phase benzene using laser source 99: 166436r Gaseous alkenes, satellite structure in 86: 170244a Gaseous barium halides, ligand-field splitting of Ba in 92: 155595w Gaseous oxyanions salts 86: 130688s Germabenzene and 97: 72462c Germane trifluoromethyl derivs. 96: 207880q Germanium difluoride 97: 153447d Germanium dihalides 97: 153467k 90: 78883t Germanium, selenium and tellurium 87: 159294s Glycidyl and thioglycidyl ethers 103: 70815p Glyoxal, MO calcns. in reI. to conformatn.of 87: 183832m 77: 81900h Gold 77: 54483t Gold 77: 81g00h Gold 85: 185512q Group lIB halides 79: 120297e Group lIB halides 80: 114264w Group lIB metal halides 81 : 84126d Group III oxides 100: 218463h Group IlIA element halides and methyl cmpds. 83: 185985e Group IlIA metal halides and methylmetal halides 84: 142862r Group IlIA pnictides, surface energy levels in reI. to 86: 198793c Group IV and Group V amorphous elements, valence orbitals in relation to 87: 143807a Group IV derivs. of benzene and naphthalene 94: 46565g Group IV dialkylamide 82: 148044f Group IV halides 91 : 166050v Group IV tetrahalides and carbon tetrahalides 99: 45674h Group IV tetrahalides and tetramethyls 93: 138322h Group IVA alkyl hydrides 92: 85509v Group IVA alkyls and amides and halides 85: 101842m Group IVA aryl sulfides 84: 104761f Group IVA cmpds. 78: 64926z Group IVA element cmpds. 78: 142238t Group IVA element tetrafluoro- and tetramethyl cmpds. 77: 107190d Group IVA element-sulfur bonded ring cmpds. 100: 129273d Group IVA hexamethyl derivs. 95: 186461x Group IVA organic cmpds. 87: 21774s Group IVA tetra-Ph derivs. 100: 103525n Group IVA tetrachlorides 91 : 184562t Group IVA tetrafluorides, uv 83: 199988v 26

Group IVA tetrahydrides 76: 39983s Group IVA tetramethyl cmpds. 77: 41157q Group IVa tetrahalides 89: 68166b Group VA alkyl derivs., perfluoroalkyl effects in 96: 112893g Group VA chalcogenides using synchrotron radiation 97: 205301y Group VA cmpds., ionization potential in relation to 100: 68422c Group VA element oxides and sulfides 86: 36114e Group VA element tri-Me cmpds 81 : 62703n Group VA fluorides and Group VA halide oxides 76: 79112p Group VA trihalides 99: 13347n Group VA trihydrides and trihalides 101 : 219066p Group VIA heterocyclic cmpds. orbital mlxlng in reI. to 81 : 119409c Group VIA org. cmpds., conformation in relation to 100 : 67527d Group VIa hexacarbonyls 80: 42688n Group VIa cycloheptatriene and mesitylene complexes 86: 197469q Group. VIa metal trihalo phosphine carbonyls 89: 120412v Hafnium tetrahydroborate and zirconium tetrahydroborate 96: 60377v Halo-substituted benzene ions 92: 5743d Halo-substituted methane and 96: 60404b Haloacetaldehydes 103: 122809m Haloacetones 86: 71146p Halobenzene cations, fluorescence quantum yield and lifetime from 97: 226505h Halobenzenes 94: . 83173y Halobenzenes 96: 68139q Halobenzenes 80: 14403x Halobicycloalkanes 102: 148576n Haloderivs. of germane and silane 76: 8709c Haloethylenes, MO and substituent effects in relation to 80: 107485r Haloferrocenes 102: 24778k Halogen atoms 89: 51059w Halogen and isocyanates 92: 188853g Halogen diat. mol cations 101 : 180485x Halogen monofluorides 90: 78888y Halogen pentafluorides and sulfur chloride fluoride 80: 42681e Halogen thiocy~nates 95: 540 13m Halogen- and Hydrogen-bridged triosmium decacarbonyls 99: 166380t Halogen-contg. mols. in gas phase 94: 217089m Halogen-substituted cmpds. 86: 130668k Halogen-substituted dicarbonhexaborane 91 : 201788r Halogenated benzenes and toluenes 84: 120697p and Me halides, spin polarization effects in, with unpolarized source 100 : 129294m Halomethanes i8: 166463p Halomethanes, MO calcn. in relation to 99: 21808d Halomethanes, MO calcns. in reI. to 96: 141912t Halomethyl cyanides and halopropynes 87: 21820d Halomethyl radicals 100: 174143x Halomethylphosphine chalcogenides 86: 36115f Halopentaborane(9) substituted deriv., subst. effects in 84: 128484n Halophosphine 100 : 68497b Halothiocarbonyl cmpds. assignment of 82: 42472d 2-Halothiophenes 100 : 218516c 27

4-Halotoluenes 100: 218515b 5-Halourac ils 90: 22047f Harmine derivs. 90: 114929y Heavy atoms and mols. 93: 123282w Helicenes 83: 211131v 82: 162598w Helium and hydrogen mols. 82: 162631b Helium and xenon, intercannel coupling effects on resonant 100: 218459m Helium group gases 92: 155591s Helium, final-state symmetry of pos. ion in 96: 152037n Helium, nitrogen, and oxygen, differential and partial cross sections for ionization in relation to 99: 13419n Helium-group gases, outer-subshell 81 : 143959c Heteroatom contg. mols., heteroatom parameters in reI. to 96: 94443d Heteroatom contg. org. cmpds. 100: 156151u Heterobicyclooctadienes 91 : 90925m Heterocmpds. contg. first-row elements 96: 132648j Heterocycles 96: 19557r Heterocycles contg. oxygen and sulfur, lone-pair electron interactions by 99: 79488r Heterocyclic aromatic mols. 93: 158594b Heterocyclic base complexes 94: 148047g Heterocyclic benzo derivs. 100: 102416r Heterocyclic cmpds. 93: 238086c Heterocyclic cmpds. 94: 102312m Heterocyclic cmpds. 88: 104285e Heterocyclic cmpds. 77: 151124J Heterocyclic cmpds. 82: 169631k Heterocyclic compds. 99: 157454t Heterocyclic cyclophanes, MO calcns. and 89: 196775m Heterocyclic indene analogs 86: 71330u . Heterocyclobutanes 87: 21828n Hexachlorobenzene 94: 217052u Hexacyanoferrate 94: 73714m Hexacyanoferrate ion 88: 81171y Hexadiyne, photoionizatn. in relation to 89: 75158d Hexadiynes 89: 41735z Hexafluorobenzene and its isomers 89: 107155u Hexafluorobenzene, Rydberg series converging to estate of hexafluorobenzene cation in relation to 98: 188515x Hexafluorobicyclohexadiene 84: 3961j 80: 69901p Hexahydropyridazine, conformation in relation to 78: 135538n Hexakis(trimethylsilyl)butyne 90: 103038f Hexamethyldistannane, tin 5p photoionization 103: 95527J Hexamethylethane and hexamethyldisilane radical cations 95: 52193w Hexamethylidenebicyclooctane 93: 113401v Hexamethylphosphoric triamide, yield and mean free path 98: 25091s Hexatriacontane, angular- and light-polarization- dependent valence 97: 101203b Hexatriene 89: 107022y Hexatriene isomers and methylpentatrienes 90: 143941b Hexfluoroacetoneimine 86: 54579q Hindered phenols & benzene derivs. 100 : .120434z 28

Histamine, electron structure in relation to 91 : 56117q Homoallylic Me ethers 83: 42481b Homobarrelene derive 98: 125247r Hydantoin, methylhydantoin, and urazole 97: 109432w 78: 166744f Hydrazine and its monoalkyl and dialkyl derivs. 82: 177822p Hydrazine derivs. 84: 89425x Hydrazine methyl derivs. 84: 4304J Hydrazobenzenes, conformation in relation to 87: 52649J Hydrazoic acid 85: 133663v Hydrazoic acid and azide, uv and x-ray 83: 139563t Hydride ion in laser beam, resonances in, elec. field effects on 88: 161148m Hydrides, in electronic structure study 92: 138112u Hydrido alkynyl ruthenium & cluster cmpds. 98: 107519b Hydrocarbons 93: 84576y Hydrocarbons 88: 37039n Hydrocarbons 88: 49789v Hydrocarbons contg. norbornadienylidene or quadricyclanylidene groups 92: 127990c Hydrocarbons contg. norbornadienylidene or quadricyclanylidene groups . 92: 127990c Hydrocarbons, calcn. of ionization in relation to 89: 179381n using synchrotron radiation source, angle-resolved 99: 113375p Hydrogen and deuterium, angular distribution in 96: 207882s Hydrogen and its deuterated isomers, rotationally resolve 97: 82230q Hydrogen atom-silicon system with oxygen contamination 96: 225985g , Cooper min. in cross section 102 : 87002y Hydrogen bromide, branding ratios for 103: 169221d Hydrogen chloride 97: 171879a 96: 207905b Hydrogen cyanide and deuterium cyanide, uv 83: 139553q Hydrogen cyanide and deuterium cyanide, vibronic coupling 90: 194829d Hydrogen cyanide and methiophosphide 80: 89310y Hydrogen cyanide and related cmpds. 85: 39096r Hydrogen cyanide monopos. ion, anomalous effects in 89: 51061r Hydrogen electronically excited states 98: 169962z 76: 29408u Hydrogen fluoride 85: 151523d Hydrogen fluoride and neon, many-electron effects in explanation of satellites in 86: 197493t Hydrogen halides 83: 88279v & Me iodide 100 : 200347p Hydrogen iodide, spin-orbit autoionization 103: 112704J Hydrogen mol. in excited state 100: 129326y Hydrogen mol., angular distribution in 100 : 129325x Hydrogen mol., cross section calcns. for 103: 186299c Hydrogen mol., photoelectron angular dist. in 94: 112135v 80: 139220s Hydrogen peroxide and 82: 24109m and 95: 88647m Hydrogen sulfide, angular dist. in, measured with neon and helium resonance lines 93: 212857e 29

Hydrogen sulfide, branching ratios and asymmetry parameters in relation to 103: 169208e Hydrogen sulfide, following multiphoton ionization 97: 30804k Hydrogen, nitrogen, and carbon monoxide, angular dist. 92: 49831k Hydrogen, rotationally resolved photoelectron angular distributions for hydrogen cation from 97: 63598z Hydrogen-bonded complexes between acids and amines 92: 146102f Hydrogen-bonded complexes of azaindole or phenol 101 : 100726p radical, vibrational struct. of cation from 96: 171629y Hydroquinone Me alkyl ethers 83: 27091f Hydrotris(pyrazolyl)borates 94: 183028y Hydroxy azo cmpds., tautomerism in relation to 93: 25763j Hydroxy- and mercaptopyridine, tautomerization study of 92: 146058w Hydroxy- and mercaptopyridines, tautomerism in reI. to 88: 104458p Hydroxy- and methoxycyclohexanone 86: 88593e (Hydroxyalkyl)isoalloxazines, intramol. hydrogen bond. 96: 180570z Hydroxyazobenzenes 95: 5996a S-Hydroxyethyldimethylamine N-oxide 82: 169599f Hydroxyl & deuteriohydroxyl radicals 100: 218417w Hydroxylamine and methylhydroxylamine 87: 183857y Hydroxylamine, MO study of first two bands in 97: 226460q Hydroxymethyl radical 102 : 35927j 78: 166743e Hypoxanthine, guanine, and their Me derivs. 92: 197419x Imidazole and methylimidazoles 90: 185867n Imidazoles, ionization energies in relation to, sUbstituent effects on 91 : 56026j anion 103 : 202997m Imino phosphoranes 92: 13335n Iminophenalenamine, calcn. of 90: 167825t Indandione and heterocyclic analogs 87: 21768t Indium and thallium cyclopentadienides 90: 102920a lH-Indole-3-alkanoic acids 90: 102932f Indoles 88: 104523f Inorg. and organometallic mols. 87: 21824h Inorg. cmpds. 91 : 166066e Inorg. cmpds., bonding in relation to 91 : 131738y Intramol. hydroge-bonded systems of 2-bromoethanol and 2-chloroethanol 101 : 100750z Iodine and mercuric iodide, relativistic calcn of 92: 203836z Iodine atoms from mol. iodine photodissocn. 93: 84580v Iodine-doped polyacetylene 93: 140529z Iodobenzene cation, coincidence of photoion with 98: 152332w Iodobenzenes 87: 133298w 83: 18563j Iodomethane, electron photodetachment from transient neg. ions in relation to 103: 14034w Ionic cmpds., valence-shell satellites in, photo-induced ~ovalency in relation to 100: 218499z 3d Ions 94: 129959q Iron 90: 131559v Iron and cobalt cluster cmpds. 97: 56003y Iron and ruthenium carbonyl cycloalkene complexes 86: 36120d 30

Iron and ruthenium tetramethylidene bicyclooctene complexes 102 : 185251y Iron carbido carbonyl clusters 96: 43507v Iron carbonyl trifluorophosphine complexes 88: 81529w Iron cyanide complexes 86: 163308w Iron diboryl complex 98: 89595a Iron complexes 94: 64934f Iron hydride anion and hydride anion 99: 30261x Iron methylene-bridged dinuclear carbonyl complex 95: 212555w Iron monoxide, laser-excited 87: 31618h Iron nitrosyl complexes 87: 93195b Iron nitrosyls 87: 191792p Iron pentacarbonyl 99: 166438t Iron pentacarbonyl, axial and equatorial carbonyl groups 88: 81523q Iron tetracarbonyl isocyanide complexes 102 : 69689y Iron tetracarbonyl trimethylamine complex, photochem. 93: 159080t Iron tetrakis(methylene)oxabicycloheptane complexes 96: 122968z Iron tricarbonyl 1,4-dimethyltetraazadiene and related complexes 94: 164960e Iron tricarbonyl trimethylenemethane 84 : 142860p Iron tricaronyl cyclobutadiene 83: 211114s Iron-thionine complex 89: 170879y Ironcyclopentadienyyl complexes with phosphines 89: 206997b Isocyanates, , and 92: 119215p 78: 90777w Isocyanides, conjugation in relation to 86: 88524h Isoindole and its benzo derivs. 85: 32178k Isomerization of dimethylpyrazolinethione and dimethyltriazolinethione in relation to 99: 121577w Isonitriles and nitriles 93: 212848c Isoperthiocyanic acid 87: 110669d Isopropylidenebenzonorbornenes 96: 141915w Isoquinolinium ylide 85: 45724k Isospectral mols. 89: 214744g Isoxazole and dimethylisoxazole, ang. dist. in 98: 62684h Isoxazole, oxazole, and oxadiazole, through-bond inter- action in 87: 167369k Jet-cooled naphthalene, intramol. relaxation processes in 102 : 175665x K-shell, of boron fluoride 100: 27786f Ketene 89: 75061s Ketene derivs. 95: 114303t Ketene mercaptals 89: 107651c Ketenimines, MO calcns in relation to 93: 185234r Ketoprofen 84: 43549n Krypton and xenon in autoionization region, angular distribution in 102 : 86979k , and 99: 96283n Lactams 103: 195736v Lanthanide chlorides in gas phase 96: 226001v Lanthanide complexes with octaethylporphyrin and tetraphenylporphine 92: 101986f Lanthanide trifluorides, satellite excitations in 86: 98626g Lanthanide trihalides 98: 206984f 31

Lanthanides 83: 88275r 86: 10222p Lead-phthalocyanine complex with synchrotron rad. source 99: 79559q Limonene 102 : 102591k Lithium and vapors, inner-shell 98: 116391f , core exciton in relation to 101 : 119861a Lithium fluoride, exoelectron energy distribution 97: 15607e Lithium halide monomers and dimers 91 : 184557v Lithium halide vapors, monomer and dimer electronic structures in relation to 91 : 166073e Lithium halides in vapor state 92: 119207n 89: 188525q Lithium vapor, resonances in 90: 177748j bromide 95: 70291f Magnesium chloride 93: 227859f 84: 157751c Maleimide and succinimide and N-Me derivs., fine struct. 97: 171853n Malonaldehyde and acetylacetone fluoro derivs. 82: 148054j Manganese and manganese difluoride 78: 153539t Manganese and molybdenum complexes with carbonyl and other ligands 93: 101674y Manganese and carbonyls and pentacarbonyl halides 84: 24192z Manganese chloride oxide and manganese fluoride oxide 88: 30060d Manganese halides, shake-up transitions in relation to satellite in 86: 130689t Manganese pentacarbonyl cmpds. 77: 132990x Manganese pentacarbonyl halides, core binding energy in assignments in 98: 25110x Manganese, resonant 98: 80986n Me Ph telluride 86: 155012e Me allenyl ether and sulfide 93: 219987f Me amines 83: 27132v 4-Me and 4-phenyl-1,2,4-triazolinedione 103: 169183t Me cyanide and Me isocyanide 76: 146874d Me dimethylphosphinothioite, dimethylphosphinoselenite and their arsenic analogs 95: 79499n Me esters 103: 95526h Me ether-boron trifluoride donor-acceptor complex 96: 94433a Me halides 86: 105243k Me iodide, inner-shell 101 : 81130w Me isocyanide and its borane complex 96: 26596f Me methylcyclopropyl ketones MO in reI. to 86: 138951t Me propionate and its isomeric esters 94: 64710e Me radical 86: 88619t Me radical and ions 102 : 112536k Me styryl sulfones, substituent effect on 101 : 22837j Me sulfide-hydrofluoric acid trimer complex 99: 194275f Me tri-tert-butylcyclobutadienecarboxylate, uv 83: 35380q 3-Membered heterocycles 93: 113699y 5-Membered heterocyclic compds. 102 : 78216u Mercapto radicals, third ionization peak in 96: 60383u 102 : 194520n Mercury 76: 19892h Mercury and rare gases, anisotropy in relation to 77: 41148n 32

Mercury in autoionization region, spin polarization 96: 60500e Mercury in solid and gaseous state 85: 114332v Mercury using unpolarized light, electron polarization effects in, as new aspect of Fano effect 96: 152038p Mercury, 4f, 5p and 5d subshell 99: 30217g Mercury, collective effects in photoionization of outer shells in relation to 103: 29645v Mercury, in study of d. of energy levels 79: 149519j Mercury, relativistic interactions in, theory of 91: 226465v Mesitylene and related cmpds. 81 : 2983u [2.2]Metacyclo-2,6-pyridinophane, MO calcns. and 84: 43118w Metal a-diketonates and a-diketones in vapor phase 86: 163306u Metal carbonyls 80: 139232x Metal halides, for ionization from 5d subshells 101 : 180411q Metal halides, uv 82: 162830r Metal hexacarbonyls, shake-up satellite structures in 88: 128112t Metal methylaminobis(difluorophosphine) complexes in gaseous phase 90: 159149f Metal sulfide nonacarbonyl clusters 99: 149019q Metal trifluorophosphine and hydrido(trifluorophosphine) complexes 83: 211112q Metal vapors at high temp. 86: 98629k Metal vapors at high temp. 86: 98629k Metalated dihydropyrazines 95: 114210e Metallocenes 78: 3412g Metallooctaethylporphyrins 90: 195246y Metallothioneins 84: 21141z Methane 80: 14412z Methane & ammonia & water, satellite structures in ls-spectra of, MO calcn. of 100 : 42350c Methane and dimethylmercury 89: 97194k Methane and fluoromethanes 83: 105952d Methane chlorofluoro derivs 84: 134163u Methane chlorofluoro derivs. 88: 119869g Methane chlorofluoro derivs., ion coincidence spectra of electrons in 102 : 212131t Methane halo derivs. 19: 36906v Methane halo derivs., asymmetry parameters for 103: 169185v Methane mixed halo derivs., uv 82: 148059q Methanesulfenyl halides 92: 110118b Methanocyclodecapentaene, aromaticity in relation to 78: 22308u Methanol and deuterated derivs. 81: 111210f Methanol cation, dissocn. path in reI. to 98: 25092t Methanol hydrogen bonded vapor dimer 98: 116445b Methanol, first band of 94: 129952g Methide 89: 23652r Methinyltricobalt nonacarbonyl clusters in gaseous phase 96: 112821p Methoxide and thiomethoxide ions 90: 21161x Methoxy- and (methylthio)boranes, charge d. and MO 81 : 3015s Methoxybenzene and its derivs. 91 : 19657v Methyl 79: 36910s Methyl & silyl halides, electronic struct. in reI. to 71: 61919q Methyl dithiocarbazates and nickel dithiocarbazates 80: 21196k Methyl iodide and hydrogen iodide 81 : 8285q 33

Methyl nitrate 85: 133677c Methyl substituted hexatrienes 84: 82254g Methyl(tertiary phosphine) and -gold complexes, chern. reactivity in relation to 89: 19643ge Methyl (trimethylphosphine)gold 97: 55944u Methyl- & dirnethylketene, calcn. of 100: 156112g Methyl- and phenylhydrazones 83: 163178s Methyl- and silyl-substituted benzenes 87: 151569q Methyl-substituted 1,3-dioxane 100: 59101v Methyl-substituted [2.2]paracyclophanes . 96: 84915v Methyl-substituted biphenyl 100: 120189y Methylallylradicals 101 : 229825z fluoroderivs. 96: 132651e Methylamines and methylpiperidines 87: 38363e Methylanthracene 80: 144943j Methylated and perfluoromethylated 99: 195133v Methylated anilines 96: 84923w Methylated butadienes and hexatrienes 79 :. 77590f Methylated digermyl and disilyl chalcogenides 88: 21852m Methylbenz[a]anthracenes 95: 168270y 2-Methylbenzotriazole 94: 29707n Methylborinato transition metal complexes, electronic structure in relation to 102 : 204093s Methylbromogermanes 94: 74251v Methylchloramine and methyldichloramine 90: 86200h Methylcycloalkanediones 98: 88492u Methylcyclopentindene 103 : 214734m Methyldioxaphosphorinane diastereoisomers 76: 139630t Methylene anion 100: 148161" Methylene anion 95 : 15653a Methylene anion, calcn. of 103: 223813p Methylene dihalides 101 : 54134u Methylene(1-), 85: 77408b Methylene-bis[dicarbonyl(cyclopentadienyl)manganese] 95: 202776e Methylenebicyclononatriene 78: 123496j Methylenebis[dicarbonyl(cyclopentadienyl)manganese] 94: 208004c Methylenecyclobutanes, conjugation and 94: 102576a Methylenecyclohexadiene and its radical cation and their precursors 103: 141357d Methylenecyclohexane, -thiacyclohexane, -methyl- piperidine, and - thiaperhydronaphthalene derivs. 94: 173794f Methylenedioxy- and methylthiodimethyltryptamines 97: 155950m Methylenenorbornadiene 77: 743921" Methylenenortriquinacenes 88: 151826s Methyleneoxetane, oxetanone and propiolactone 92: 1804831" Methylenepentacyclononane 87: 200611h Methylenesulfur tetrafluoride 92: 5809ge Methylenimine 83: 205412w Methylhaloboranes 85: 93312w Methylhydroxypyridine-dichromium & dimolybdenum cmplxs. 93: 212829x Methylidenecyclopropanes 89: 23300z Methylidynephosphines 98: 54047n Methylphenoxasilin and ethylmethylphenazasiline MO calcns. in relation to 98: 179456b 34

Methylphenyl(thiobenzoylmethylene)thiapyran 97: 181610v Methylphosphaanthracene 84: 105688t Methylpyrrylcyclophosphazenes 96: 217936b Methylstyrene derivs. 93: 220307r Methyltetrahydropyridine 92: 163819n Methylthiazolidine derivs. 88: 136022h Methylthio arom. cmpds. 79: 31317u Methyltin chloride 87: 38380h Methyltin chlorides 92: 128002u Mixed-metal carbonyl sulfide clusters 99: 45657e Mol. nitrogen, angular dist. in 90: 38605p Molybdenum & molybdenum oxides, electronic structure 100 : 94003m Molybdenum & ruthenium, electronic struct. in reI. to 76: 39587r Molybdenum acetate and formate complex, carbon 1s satellite peaks in 96: 26621k Molybdenum acetate contg. metal-metal-quadruple bonds in detn. of bonding contribution of a-orbital electron 98: 188490k Molybdenum and tungsten alkoxy complexes with double bonds 103: 203167c Molybdenum and tungsten cmpds. 96: 60074u Molybdenum cmpds. 83: 88238f Molybdenum complexes with carboxylic acids, uv 82: 177845y Molybdenum nitrosyl complexes 81 : 19017e Molybdenum sulfido cluster cmpds. 96: 173297n Molybdenum-Bu sulfide complex, MO interpretation of 98: 62683g Mono-, di- and trisulfides of dimethylnaphthalene 94: 83388x Mono-, di-, and triallylamine 85: 20257x Monosubstituted benzene, asym. parameter and ionization potential from 90: 86204n Morphlnans 83: 179339f Morphine and nalorphine 84: 13589ge N-Arylazacycloalkanes 97: 38339h N-Arylsulfilimines and N-aryliminophospharane 88: 189449j N-Benzylideneanilines 88: 49849q N-Bromo methanamines 89: 207013q N-Halosuccinimides 88: 151644f N-Phenylpyrroles 100: 14757x N-Vinylphthalimide, in study of conjugation effects 98: 62653x Nanocyclic arom. hydrocarbons, polarizat. energy in reI. 98: 53003h Naphthalene and quinonoid heterocycles 84: 104828b Naphthalene derivs. 83: 130689f Naphthalene peridisulfide 88: 151827t Naphthobisthiadiazine 100 : 5380s Naphthobisthiadiazine 102 : 5513d Naphthoquinone intramol. charge-transfer complexes 96: 84935b Naphthoquinones 94: 3343r Neon 85: 12131m Neon, satellite lines in 102 : 194492e Neopentane and tetramethylsilane and -germane 101 : 23626b Nickel pentadienyl complex, electronic struct. in reI. to 96: 207830y Nickel tetracarbonyl 87: 143790q Nickel thiocarbonato complex 80: 33376g Nickel, correlation effects in relation to 96: 43492m Nicotinic acid analogs 98: 125003h Nitric oxide 103 : 61976q 35

Nitric oxide 92: 31605e Nitric oxide 76: 8697x Nitric oxide 79: 120288c Nitric oxide and zenon, multiphoton ionization effects in 98: 43627a Nitric oxide following 4-photon ionization 95: 70585e Nitric oxide valence orbitals, asymmetry parameters for 96: 77103a Nitric oxide, complete sepn. of rotational levels of cation produced in 102: 53412s Nitric oxide, multiphoton ionization study by 101: 14438q Nitric oxide, resonance-enhanced multiphoton ionization 99: 203234w Nitric oxide, rotationally resolved 100: 94004n Nitric oxide, shape resonance effects in 96: 112848w Nitriles 100: 50960s Nitro olefins 93: 167093q Nitroalkanes, dimethylnitramine, and dimethylnitrosamine 85: 108027h Nitroaniline and aminobenzonitrile, charge-transfer rxns. 98: 142618e Nitroaniline, ab initio CI calcn. for core-hole states 97: 226508m Nitroaniline, core ionization in relation to 91: 74078g Nitroaniline, satellite structure of, theory of 100: 111622g Ni troanilines 79: 110094x Nitroanilines 79: 120284y Nitroanilines, MO calcns. in relation to 103: 37048t Nitrobenzene, , and nitromethane, angular distribution in 97: 136145m Nitrobenzenes 91: 169053y Nitrogen 78: 130130p Nitrogen 84: 187264p Nitrogen & oxygen mols., MC electron propagator in calcn 100: 74136d Nitrogen ls, of homologous series of sym. cyanine dyes 100: 122747c Nitrog~n heteroaroms. 99: 21800v Nitrogen mol. produced by microwave discharge or reaction between nitrogen atoms and nitric oxide, non-Boltzmann vibrational excitation in relation to 101: 45839a Nitrogen mol., rotational intensity distribution for 102: 212091e Nitrogen mol., shaped resonance-enhanced nuclear motion effects in 91: 184576a Nitrogen monoxide 100: 94037a Nitrogen monoxide 101: 219068r Nitrogen oxide sulfide 95: 49807u Nitrogen oxides 91: 65845c , inversion barrier of monopos. cation in relation to 101: 237739q Nitrogen trifluoride, inversion vibrational states of nitrogen trifluoride cation in relation to 103: 45331 v Nitrogen using synchrotron radiation source 97: 82250w Ni trogen y lides 91: 90947v Nitrogen, angular distribution for major bands in 99: 202948v Nitrogen, multiphoton ionization in 101: 237740h Nitrogen, nitric oxide and oxygen 97: 153438b Nitrogen, using synchrotron source in Hopfield-band region 86: 24198x Nitrogen-oxygen mixts. in elec. discharges 97: 117742n Nitroimidazoles, bioI. activity in relation to 91: 38395z Nitroindazole derivs., MO caicn. in 100: 174207w 36

Nitromethane and Me nitrite ions 100: 120207c Nitromethane or Me nitrite 98: 142799q Nitronaphthylamines 89: 107016z Nitrones and nitrile oxides 87: 38357f Nitrophenols and nitroanisoles, uv 83: 68747t Nitrosamine 83: 146961z Nitrosated benzene and protonated nitrosobenzene 92: 128061n Nitroso and thionitroso chromium complexes 92: 197438c Nitroso cmpds. 85: 77002q Nitroso cmpds., form & ionicity in relation to 100: 182587k Nitroso derivs., in electronic structure study 87: 31602y Nitrosobenzene and nitric oxide, in vapor and condensed phases 103 : 104386s Nitrosomethane, tert-nitrosobutane, and trihalonitrosomethanes 93: 185292h Nitrosyl chloride 84: 171883d Nitrosyl cyanide 95: 33095z Nitrosyl cyanide and it cation & radical anion 102 : 157395e Nitrosyl halides 86: 180254t Nitrous oxide cation 99: 96329g Nitrous oxide cation, asymmetry parameters and partial cross sections for 99: 13426n Nitrous oxide in autoionization study, angle­ 103: 169247s Nitrous oxide, kinetic energy distribution of dissociative products in 102 : 14520f Nitrous oxide, predissocn. in relation to 98: 152206h Nitrous oxide, using synchrotron radiation source, angle-resolved 99: 30308t Nitrous oxide, vibronic struct. of 3rd band in 97: 117767z anion in its deuterated in log 99: 13401a Nitryl halides and nitrosyl halides, uv 83: 199989w Noble metals and molybdenum disulfide, uv 82: 177857d Noble metals, energy band structure in relation to 101 : 30639m Noble metals, uv 82: 177859f Nonacarbonylmethylidynetricarbonyl derivs., electron configuration in relation to 97: 6481g Nonarom. Schiff bases 96: 6016p Nonarom. azomethine cmpds. 87: 21783u Nonchlorotrirhenium 91 : 184569a Nonconjugated alkadiynes 92: 180562r Nonconjugated aryl ole fins 90: 54197w Nonconjugated , coupled chromophore model for 98: 4192k Nonconjugated dienes, substituent effects on 87: 167009t Nonhydrogen-like atoms and ions 99: 149025p Norbornadiene 77: 120100u Norbornadienes 99: 69875a Norbornadienes, cycloaddn. rxn in relation to 93: 203548c Norbornane, its derivs. and thioanalogs 93: 212841v Norbornenedicarboxylic anhydrides, Diels-Alder reactivity 97: 181439w Norbornenols 86: 88594f Norbornyl iodide isomers 102 : 95113a Norbornyl- and norbornenyl-fused fulvene systems 98: 159926b Norcaradiene analogs, peroxidn. and stereochem. 86: 16227r Nortricyclane phosphorus and silicon cages 99: 175923z 37

Nortricyclane triantimony, triarsenic and triphosphorus cage compds. 103: 203160v Nortricyclene and triasterane 76: 92782b Nucleic acids and their parent cmpds. 86: 73049h Octachlorofulvalene, MO ordering in 87: 133650e Octafluoronaphthalene, shake-up sattelites in 101 : 237742k Octahydrodimethanonaphthalenes, orbital interactions 97: 23132m Octamethylcyclododeca-l,3,7,9-tetrayne, antiaromaticity 88: 97141z Octatetraene 92: 21886h Org. aerosols 91 : 146013m Org. and inorg. cmpds. 97: 101174t Org. and misc. cmpds. 97: 190738v Org. anions and hydroperoxyl anion 102 : 102897q Org. cmpds. 87: 21801y Org. disulfides 80: 114635t Org. dye vapor mol. beam 102 : 14497d Org. fluorocmpds. 95: 88648n Org. halides 101 : 54384a Org. halo cmpds. 96: 225986h Org. liqs., ionization energy detn. from 103: 112735v Org. mols. 102 : 140281s Org. mols. 100 : 218423v Org. mols. 100: 218423v Org. mols., MO calcns. for 90: 130188m Org. mols., MO calcns. in relation to 100 : 33806d Org. oxo cmpds., hole mixing effects on, calcn. of 96: 171643y Org. oxo-cmpds. 93: 241812h Org. photoconductors 98: 9121y Organomercury cmpds. 100 : 103533p Organomercury cmpds. 94: 217062x Organomercury cmpds., sp2-hybridized carbon-mercury bond in relation to 96: 122934k Organometallic carbonyl osmium clusters 97: 39117w Organometallic cmpds. 98: 126331a Organophosphorus compds. 101 : 171381h Organosilicon cmpds. 100 : 103429j Organosilicon cmpds., MO calcns. in relation to 98: 72222v Orthothiocarbonates, study of spiroconjugation by 87: 67461r Osmium carbonyl cluster complexes 97: 153421 r and , uv 81 : 129530z Oxabicyclononanes, mass spectra in relation to 99: 104609r 9-0xabicyclo[4.2.1]nonenes, hyperconjugation study by 86: 121140e Oxalic acid 86: 110738q Oxalic acid and its derivs and urea 83: 11986x trans-Oxalyl fluoride 89: 188641f Oxalyl halides 89: 5582p Oxalyl halides 86: 163309x Oxathiolane and related cmpds. 99: 81536v Oxazolones 88: 169207a Oxiranes and thiiranes, substituent effects on 87: 166991v Oxygen 91 : 166046y Oxygen 87: 93213f Oxygen 91: 149075q Oxygen 76: 119806b 38

Oxygen 83: 68722f Oxygen and sulfur heterocycles 77: 100523f Oxygen atoms 81 : 43770r and sulfur fluoride 91 : 149074p Oxygen in chromium hexacarbonyl, CI calcns. of 100: 41968y Oxygen mol. using synchrotron radiation source 97: 226498h Oxygen-free and oxygen-doped terphenyl 98: 80974g Oxyligated cmpds., useful in catalysis 99: 221666t Oxypentamethylpiperidinol 98: 53002g Ozone 101 : 100749y Ozone 81: 31595z Ozone, complete active space SCF calcn. of potential surface in relation to 99: 79546h ion 90: 212807b Palladium hydride 89: 50702p Pallad ium ox ide 92: 138241k Pentaborane 79: 120291y Pentacarbonyl(selenocarbonyl)chromium 90: 95013b Pentacarbonyl(trifluorosilyl)manganese 83: 27220x Pentacarbonylmanganese halides 78: 104218d Pentacarbonylmethylmanganese and pentacarbonyl(trifluoro- methyl)manganese, three sep. ionizatns. in reI. to line shapes in 80: 76421k Pentacarbonyls of chromium, molybdenum and tungsten 89: 82629m Pentacene 81 : 161087w Pentachlorobenzene, tetrachloro-, and trichlorbenzenes 94: 217051t Pentacyclododecadiene 90: 71520p Pentacyclononane derivs. 89: 23540c Pentacycloundecane 101 : 190975w Pentacycloundecane derivs. 79: 91665r Pentafluorobenzonitrile 93: 238101d Pentahaptocycloalkenylmanganese tricarbonyls, correlation with MO calcns. 82: 78669n (Pentamethylcyclopentadienyl)uranium cmpds., vs. calculated values 99: 158572s Pentamethyldisilane 76: 85118m Pentamethyltantalum and hexamethyltungsten 83: 105938d Pentaprismane vs. cubane 98: 71120y Pentatetraene 86: 170259j Perchlorate ion 78: 166745g Perchloryl fluoride and sulfuryl fluoride 77: 27185r Perfluorinated arenes 90: 167496m Perfluorocyclobutanone and -cyclobutanedione 103 : 104479z Perfluorocyclobutene trimer 82: 169609j Perfluoroderivs. of trisannelated benzenes and tetrakisannelated cyclooctatetraenes 101 : 6446a Perfluoroethane 93: 94370r Perfluoromethylated germanium halides 96: 52422r Perhalogenated methanes 94: 112137x Perhydrotetraazadiborine derivs. 81 : 168713a Peri-aminonaphthalenes 81 : 62708t Pericyclynes 103: 177919c Permethyl polygermanes 96: 187604x Permethylcyclopolysilanes 92: 21776x 39

Peroxides 84: 179055f Peroxides and oxonides, gas conformations and 92: 41205p Perxenates 84: 51923v Ph and pentafluorophenyl derivs. of sulfur 95: 167938k Ph azide 96: 198726q Ph azide, phenyldiazomethane,- benzonitrile oxides and Ph nitrones 86: 105198z Ph selenocyanate and 95: 167972s Phenalenone 101 : 151555q Phenalenone derivs. 102 : 53360y Phenazine oxide and monosubstituted derivs. 84: 120668e Phenol, alkoxy- and acyl benzenes 87: 200333u Phenol pyridine hydrogen-bonded complex 90: 103144n Phenols and benzenediols 91 : 39694w Phenoxachalcogenins 88: 189768n Phenoxazines and phenothiazines 84: 16352m Phenoxy radical 93: 212842w Phenyl and methyl substituted allenes 83: 192029z Phenyl and toly isocyanate and phenyl isothiocyanate 84: 42723c Phenyl-substituted Groups IVB catenates 102: 62348c Phenyl-substituted cyclotriphosphazenes 92: 188834b Phenylacetylene, sub$tituent effect on 96: 5778b Phenylalkynes in argon matrix, vibronic absorption spectra of radical cations in relation to 97: 190633g Phenylboranes 88: 61712x Phenylcyclopropane derivs., substituent effects on 87: 38696r o-Phenylenediamines and related cmpds. 94: 64702d Phenylhalosilanes 101 : 55168v Phenylhydrazones 85: 32177 j (Phenylimino)imidazolidines 93: 113399a (Phenylimino)thiazxolidines, -thiazines or -oxaxolidines 97: 91286q Phenyloxiranes 102 : 166204v Phenylphosphaphenanthrene and related cmpds. 80: 119794d Phenylpolysilanes & benzylsilanes, conjugatn. detn. from 83: 35089b Phenylpyridines and bipyridines, conformation and electronic structure in relation to 99: 194278j Phenylpyrimidine, structure and electron con- figuration in relation to 102 : 112522c Phenylsilaisocyanide 102 : 113581h Phenylsilanes 96: 69096k Phenylthiatriazole and its 3-oxide 83: 147434s Phisocyanide derivs. and tert-Bu isocyanide 96: 60410a Phosgene and thiophosgene 76: 119670c Phosphaalkynes, electronic struct. in relation to 99: 53850c Phosphabenzene, calcd. vs. exptl. 92: 214375z Phosphacymantrenes 92: 180506a 2-Phosphanaphthalenes 83: 8612k Phosphapropyne and other pyrolysis products of dichloroethylphosphine 91 : 211490b Phosphates and phosphites 95: 141489q Phosphenous and thiophosphenous chloride 101 : 160615m Phosphine and 76: 147086k Phosphine cyclic derivs. 102 : 212069d Phosphine oxide derivs. 101 : 211264f 40

Phosphine trifluoromethyl-substituted derivs. and chlorophosphines 83: 88268r Phosphine, exptl. & theory study of 100: 59143k Phosphine, helium-excited 99: 79493p Phosphine, phosphorus fluoride and related ions 78: 151781s Phosphine-borane complexes 96: 34347r Phosphine-substituted molybdenum carbonyls, ligand additivity in 102: 14490w Phosphines and amines, conformation effect on 103: 105069c Phosphines, gas-phase coincidence, in predissocn. study of dioxygenyl 97: 153437a Phosphinidine and phosphirene complexes 103: 201049s Phosphites, thiophites and arsenites 101: 151960t Phosphites, thiophosphites and arsenites 101: 151960t Phospholes 84: 89058e Phosphorins, measured vs. calcd. 85: 123159w Phosphorus and 86: 180286e Phosphorus cmpds. contg. 94: 207995q Phosphorus diat. and tetraat. mols. 86: 98609d Phosphorus esters, conformation and 95: 168384p Phosphorus gaseous cmpds. 100: 59147q Phosphorus heterocycles, conformation in reI. to 99: 5697m monocation 98: 134684h Phosphorus nitride 87: 46334m Phosphorus nitride 87: 143783q Phosphorus sulfide 98: 116436z Phosphorus tetraat. mol. 89: 95187r Phosphorus ylides 86: 15943j Phosphoryl chloride 87: 76104d Phosphoryl cmpds. 91: 131722p Phosphoryl halides and thiophosphoryl halides 79: 11179t Phthalazinophthalazinedione and its mono- and substituted derivs. 94: 207966f Phthalic and seleno-, telluro- and thiophthalic anhydrides 97: 23160u Phthalocyanine and metal phthalocyanine vapors 91: 19620c Phthalocyanine cmpds. 85: 101872w Phthalocyanine vapors in presence and absence of metals 92: 138239r Phthalocyanine, autoionization processes and shake-up satellites in 102: 14496c Piperazinediones 90: 103197g Piperidine and N-halopiperidines 91: 19663u Piperidine derivs. 82: 56929v Plastocyanin 83: 92622u Platinum 91: 131726t Platinum and palladium acetylene complexes. 101: 7404x Platinum complexes 77: 12098r Platinum group metal complexes with l-phenyl-3-methyl-4-phenylazopyrazole-5-thione 97: 32619c Platinum(III) acetate 93: 113902j Poly(benzimidazoles) and their salts 91: 5631 v Poly(dimethylpyrrole) 100: 94800u Poly(methyl methacrylate) and polystyrene 83: 11062m Poly(p-xylylene) 95: 228797n 41

Poly(trimethylsiloxy)benzenes 103: 105037r Poly(vinyldiene fluoride), poly(trifluoroethylene) and poly(tetrafluoroethylene) 100: 157300d Poly-2,4-hexadiyne-1,6-diol bis(p-tolenesulfonate) crystals 96: 190115u Poly[hexadiynediol bis(toluenesulfonate)] and monomer thereof, ionization threshold detn. from 98: 35110m Polyacenaphthalene, in n-electron ionization region, free rotation of arom. ring in relation to 102: 185755r Polyacetylene doped with arsenic pentafluoride 91: 166055a Polyacetylene model oligomers, MO calcn. of 96: 181882q Polyaminoboranes 103: 54127k Polyat. mols., isotope effects in 91: 184561 s Polycyclic arom. hydrocarbons and bioi. purines 93: 94377y Polycyclic azoalkanes 85: 191644a Polycyclic benzenoid hydrocarbons, electron configura­ tion in relation to 84: 3951f Polycyclic bis(exomethylene) cmpds. 100: 102615e Polycyclic hydrocarbons, correlation of phosphorescence spectra with 86: 170146v Polycycloalkanes 102: 220201f Polycycloalkyl halides 101: 229828c Polyene radical cations 101: 30489n Polyethylene and poly(fluoroethylenes) 82: 98562a Polyfluoroarom. phosphines 99: 38540h Polyhalomethanes 96: 34351n Polymethano arom.cmpds., long-range benzene-benzene interactions in relation to 101: 130063n Polynuclear arom. hydrocarbons, struct. in rei. to 94: 155890e Polynuclear arom. hydrocarbons, uv spectra correlation 86: 154170p Polypeptides, in vacuum-UV region 99: 35553d Polypeptides, in vacuum-UV region 99: 35553d Polyphenyls, intramol. band mapping of polyphenylene in relation to 102: 79502w Polyphosphines 81: 31592w Polypyridines 88: 169222b Polysilacyclalkyapolyynes 102: 220937a Polysilanes 83: 35373q Polysylylene, electronic structure in relation to 97: 56504n Polyxylylenes 88: 121800m Porphins 87: 143789w Porphyrins 91: 55684k and sodium, electron polarization in 96: 94451e 82: 24098g and 83: 68736p Potassium halides 79: 131259v Praseodymium 4d electrons 89: 171510h Propadienone and vinylketene 103: 22048u Propane 89: 97412j Propane and neopentane 86: 43037k Propargyl chlorides 89: 59354j Propel lane 103: 214621x Propellanes 79: 31106z Propellanetrione 88: 6385t 42

Propene imine 97: 226342c Propyl- and allyl-substituted amines 88: 73765e Propyl-"and isopropylbenzene 88: 15185ge Propyne and fragment ions 91 : 90746d Proteins 93: 181392t Psychotropic agents 98: 206967c Psycho tropics 87: 62381e Purine derivs. 85: 155251m Purine, adenine, and their Me derivs. 93: 70712c Purines and pyrimidines 91 : 15391f Push-pull ethylenes 86: 17062ge Pyran and p-dioxin and their dihydro analogs 89: 89963z Pyrazine 76: 160611x Pyrazinopyrazines 102: 23988s Pyrazinotricyclononane derive 97: 144170f Pyrazolinethiones, triazolinethiones and triazolium sulfides, effect of C-methylation on 88: 151632a Pyrazolones 102: 203499s 83: 8654a Pyridazine 76: 92793f Pyridine 92: 197548p Pyridine 90: 71402b Pyridine and pyridine-d5 97: 117745r Pyridine and pyridine-d5 96: 171677n Pyridine based cycloimmonium ylides 103: 177690w Pyridine derivs., quantum chern. calcn. of 97: 181338n Pyridine fluoroderivs. 76: 92798m Pyridine oxide 95: 132127t Pyridine oxide 93: 84555r Pyridine oxide and its derivs. 82: 49679k Pyridine oxides 95: 202828y Pyridine-boranes, pyridine substituents in relation to 83: 155331w 89: 196408u . Pyridinium and isoquinolinium indandione betaines 95: 167988b Pyridinium difluorotetrathiodiphosphate 78: 118606r Pyridinium ylide 100 : 138462s Pyridinoparacyclophanes 91 : 20280y 76: 92794g Pyrimidine and triazine meso ionic cmpds. 94: 191090c -type cmpds. 101 : 45718k Pyrochlore-type ruthenates 98: 209098f Pyromellitic dianhydride, dithioanhydride and and of trimellitic anhydride 91 : 149073n Pyrrole and isomers 93: 238044n Pyrrole and pyrazole, MO talcns. in rel. to 80: 95033b Pyrrole and pyrrolidine 97: 71813f Pyruvic acid and its derivs. 83: 57589s Quadricyclanes 81 : 12644y Quinodimethan and its di-Me derivs. 96: 103492y Quinodimethane, uv 83: 50492w Quinolinic anhydride and thioanhydride and methylquinolinimide 90: 71309b Quinolinimide, phthalimide, and their N-Me derivs. 89: 107518q Quinoxaline ortho-substituted derivs. 100: 76815y 43

Quiolone and 0- and N-Me deriv. 95: 23940g Radialene 90: 54071a Radioactive materials 101 : 14423f Rare gas dimers 89: 120421 x Rare gases 77: 171013a Rare gases, incident photon energy effect on satellites in spectra of 101 : 30651j Rare gases, satellite structure in, calcn. of 96: 207834c Redn. products of paracyclophane 101 : 22864r Resorcinol and dithioresorcinol derivs. 102 : 5512c Rhenium fluoride gaseous phases 91 : 184560r Rhenium fluorides and rhenium fluoride oxides 90: 65838g Rhenium pentacarbonyl halides 81 : 161853t Rhenium volatile cmpds. 89: 223640x Rhodium aminophosphine complexes, bonding in relation to 96: 6051w Rhodium carbonyl chI oro complex 91 : 201779p Rhodium pyridinedicarboxylate complexes 79: 13020n Rhodium sulfito complexes 96: 173320q Rhodium thiobenzoate complexes 87: 33035q Ring-substituted uranocenes 97: 72489s Rubidium chloride 79: 98792p Rubidium halides 86: 163302q Rubrene 90: 167493h Rubrene and tetraselenotetracene, electronic struct. 97: 169142m Ruthenium alkyne cluster 98: 215780p Ruthenium phenylpyridine bipyridine complex, compared to tris(bipyridine) analog 103: 215519g S-Tetrathianes 85: 142467m Satd. cyclic hydrocarbons 85: 84672m Satd. hydrocarbons 103: 53371y Satd. hydrocarbons 89: 23600x and , high-temp., gas-phase 102 : 175806u Selenanthrene and dibenzoselenophene, ionization pot. for 98: 43556b Selenium and tellurium 98: 116420q Seleniumdicyanide, broken symmetry effects in, calcn. of 97: 136119f Selenoformaldehyde and related cmpds. 100: 85131z Selenokene 94: 46528x Selenophene and tellurophene and thiophene 94: 74269g Selenophenes 100: 120362z Sesquinorbornene isomers, norbornene and related cmpds. 99: 157669s Sila- and germacyclopentenes 77: 163719v Silacyclanones 87: 52335d Silacyclopentene derivs. 89: 107009z Silane alkylfluoro derivs. 90: 78880q Silane derivs. 92: 5736d Silane halo derivs. 76: 85026e Silanes 84: 113979d Silanes 85: 191704v Silatranes 99: 5091j Silicon difluoride calcd. vs. exptl. 81 : 19007b Silicon difluroide 80: 89305a Silicon tetraiodide 96: 112880a Silicon- and sulfur-contg. analogs of dihydroanthracene 96: 5999z Silicon-phthalocyanine monomer and dimer 87: 38343y 44

Silver halides 85: 114335y Silver halides, uv 83: 170622k Silver halides, uv and x-ray 82: 66285w Silver porphyrins 80: 16409n Silver terpyridyl complexes 79: 73079y Silver thionamide 85: 169397a Silyl alkenes 93: 185617t Silyl radical 99: 221723j Silyl- and germylacetylenes 89: 197635c Silyl- and methylcyclopentadienes 82: 57276s Silyl-substituted phosphorus ylides 80: 81603a Silyl-substituted sulfur 91: 91632z Sily lamines 98: 126204m Silylated nitrogen heterocycles with cyclic 8n- electron conjugation 98: 89453u Silyldiazaoctenes 98: 107384d Silylhydrazines 93: 185616s Silylmethyl and neopentyl derivs. of Group IV elements 81 : 77068h Silylmethyl-substituted amines 90: 86393y Simple org. mols. 99: 30291g Simple oximes 87: 191791n . Small mols. 102 : 157412h Sodium atoms after nonresonant multiphoton ionization, angular distribution of 91: 46814z Sodium vapor excited by laser beam, hot-electron effects 96: 132691 t Spirobifluorene and of tetrabenzotricyclododecatetraene 99: 175106k Spirocyclic diene dlrivs. 98: 197315j Spirocyclopropa[1,1 ] [2,5]norbornadiene, correlation diagram in relation to 18: 70915m Spiroheptatrienes 85: 4738z Spirononatetraene 81 : 97502y Spirononatetraene and related cmpds. 82: 15764u Spirooctenes and spirononenes 81: 168947k Spirooxathiolefuranone deriv. constitution in reI. to 81 : 168769d Square-planar trans-bis(triethylphosphine)nickel-org. complexes 92: 110095s Stacked-ring silicon phthalocyanine 102: 69442n Stannaindene 98: 53980z Stiboranes, electronic structure in relation to 96: 132646g Stilbenes 98: 160070z Stilbenes 97: 91551x Styrene methyl derivs. 80: 42676g Substituted camphene derivs. 94: 175279r 2-Substituted cyclopentyl and cyclohexyl bromides 80: 2973v .> Substituted dithienyl sulfides 88: 104539r Substituted tetramethylcyclobutanones and reI. cmpds. 90: 22363f Sulfenamides 91: 197660x .. Sulfides 82: 56957c Sulfides and phosphides 84: 186872y Sulfilimine-TCNQ complex 100 : 208961e Sulfinylamines 83: 90155v Sulfonyl imide 85: 39087p Sulfoxides 71: 47545m Sulfur cmpds. 90: 46360d 45

Sulfur dibromide 91 : 149046f 81 : 31594y Sulfur difluoride 90: 46351b and thiazyl fluoride 77: 41149p Sulfur fluoro cmpds. 91 : 81334r Sulfur heterocyclic cmpds. 80: 32308z Sulfur hexafluoride 98: 43562a Sulfur hexafluoride 84: 113975z Sulfur mol. 78: 117078h Sulfur mol. in gas phase 79: 36918a Sulfur mol., uv x-ray 82: 148076t 82: 131734h Sulfur nitride, MO calcns. of 86: 22097q Sulfur nitrides 92: 206670b Sulfur tetrafluoride and related fluorosulfuranes 91 : 115005b 84: 128467 j Sulfur trioxide 85: 133668a Sulfur vapor 86: 24212x Supersonic molecular beams 98: 25106a Supersonic molecular beams 98: 152232p Sym. dihalocubanes 103: 36846q TCNQ and TTF in gas and solid phases 97: 91255d TCNQ cmpds. 90: 76765g TCNQ, electron-mol. vibration coupling in 86: 63165d -99 101 : 30643h Tellurium oxide 85: 184536p Terphenyl and its aza derivs. 92: 21648g p-Terphenyl in gaseous and solid states 84: 37120z Terphenyls 100: 67712k Tertiary phosphines 99: 212602s Tetra-tert-butyltetrahedrane 101 : 210094p Tetra-tert-butyltetrahedrane and tetra-tert- butylcyclobutadiene and related cmpds. 92: 101985e Tetraalkylhydrazines 85: 159207z Tetraalkylhydrazines and tetraalkyltetrazenes 90: 54372z Tetraalkylstannanes 91 : 192598z Tetraazacyclazine 101 : 71843a Tetraazatetracyclotetradecane and its N-oxides 97: 109303e Tetraazatricyclododecane 81 : 151145z Tetracarbonyl(ethylene) iron 99: 45656d Tetracarbonyl(ethylene) iron 91 : 219947b Tetracarbonyliron carbene complexes 94: 64933e Tetracyanoethylene and tetracyanoquinodimethane 81 : 70788j Tetracyanomethane 85: 20277d Tetracyanonaphthoquinodimethane 90: 143946g Tetracyanoquinodimethan cmpds., uv 81 : 84137h Tetrafluorobutatriene and butatriene 89: 23524a Tetrafluorodiazine isomers 80: 76411 g Tetrafluoroethylene polymers 76: 25727z Tetrafluorotetracyanoquinodimethan and its salts, shake-up satellites in 86: 63177j Tetrahaloethylenes 98: 188531z Tetrahedrane and cyclobutadiene, ESCA differentiation of isomeric hydrocarbons in relation to 96: 84925y 46

Tetrahydropyran and dioxanes, MO in relation to 19: 31102v Tetraiodoethylene, effect of relativity on 91: 126566k Tetraiodomethane, effect of relativity on 91: 126565j Tetrakis(dimethylamino)ethylene 16: 52656g Tetrakis(methylcyclopentadienyl)thorium and -uranium, electronic structure in relation to 103: 31565j Tetrakis(methylidene)cyclobutane 88: 113032x Tetrakis(methyloxopyridinato)dirhodium 93: 195810q Tetrakis(trifluorophosphine)nickel, -palladium, and -platinum complexes 82: 131133g Tetramethyl-, methyl(trifluoromethyl- and tetrakis(trifluoromethyl)germane 96: 162810t Tetramethylcyclobutanedithione and -thioxocyclobutanone 95: 96811v Tetramethylcyclobutanedithione and analogs 88: 5104j Tetramethyldiazetine 81: 111206j Tetramethylenenorbornanes and tetramethylenebicyclooctanes 91 : 101323p Tetramethylpyrazine, MO in relation to 82: 138681x

Tetramethylsilane p silicon 2p photoionizatn. in 103: 29611a Tetramethyltetramethylenetricyclooctanes 90: 120532e Tetramethylthiourea and its complexes 89: 196431c Tetranitrosylchromium 93: 16443c Tetraoxadecalins and bis(dioxolane) 96: 161138u Tetraphenylthienothiophene 89: 119010k Tetrasilabicyclo(3.3.0]octenes 89: 42109k Tetrasubstituted diphosphine disulfides 94: 183039c Tetrasulfur dinitride 91: 226462s Tetrathiabutadienes 96: 6662w Tetrathiafulvalene and bi(dithiafulvenyl) 101 : 210425x Tetrathiafulvalene and derivs. 84: 42165t Tetrathiafulvalene, diselenadithiasulvalene and tetraselenafulvalene 88: 36184q Tetrathiafulvalenes 103: 214464y Tetrathiafulvalenes and tetraselenafulvalenes 99: 31896s Tetrathiatetralin 103 : 159988v Tetrathiatetralin 103: 159988v Tetrathiofulvalene 19: 125405y Tetrathiofulvalene and tetrahydrotetrathiofulvalene 82: 30531r Tetrathiotetracene and its triiodide complex 98: 169986k Tetravinylcyclobutane, tetravinylmethane and trivinylmethane 100: 50155d Tetravinylcyclobutanes 99: 194460n Tetravinylmethane and -cyclobutane 99: 81334c Tetravinylstannane 95: 219411f /. 83: 18513n Tetrazine 11: 113264x Thalidomide and constituent parts 94: 201985m Thallium 88: 91100k Thallium 86: 195415q Thallium and dialkylthallium complexes with sulfur-contg. ligands, in sulfur-thallium bond study 96: 43416j Thallium and indium monohalides 89: 206989a Thallium and thallium iodide 92: 155589x Thallium chloride and zinc chloride in gaseous phase 95: 118304b 47

Thallium halides 99: 184475g in gaseous state 76: 106139m Thallium monochloride, band structure in reI. to 86: 36130g Thallous fluoride and its dimer 79: 47616b Thiabicycloheptane 80: 8855e Thiabicyclononane and -nonenes 82: 154634q Thiaboranes 92: 49824k Thianthrene 95: 149424k Thiathiophthene analogs 83: 192061d Thiathiophthene and derivs. 82: 154954u Thiathiophthenes 76: 92777d and its monosubstituted halo derivs. 85: 133697j Thiazole and thiadiazoles 87: 117428h and isothiazoles 89: 128681c Thiazoles, isothiazoles, and benzothiazoles, substituent effects on 87: 183798e Thiazyl chloride 84: 171882c Thiazyl halides 78: 9986u Thieno[2,3-b)thiophene and halo and methyl derivs. 85: 62337d Thioacetamides 88: 21917m Thioacetic acid and its ethyl ester 83: 185842f Thioacetone and thioacetaldehyde 82: 177817r Thioacetylaceton and related S-thioxo ketones 97: 181558j Thioacrolein and 96: 198930b Thiobenzophenones and S-oxides 89: 59362k Thioborine 80: 32321y Thiocarbonyl cmpds. 81 : 113377u Thiocarbonyl cmpds., thermal generation and 96: 141868h Thiocarbonyl fluoride and tetrafluorodithietane 78: 50331q Thiocarbonyl halides 78: 142239u 92: 87257k Thioether diamine ligands and their transition metal complexes 97: 136106z 86: 4741r Thioformaldehyde oxide 85: 39086n Thioformamide and thioformamide-d2, vibrational structure of electronic bands in 86: 29097y Thioisocoumarin and isoquinoline derivs. 78: 135136e Thioketene 86: 155069d Thioketene 87: 133631z Thioparabanic acid Me deriv. 102: 220339g . Thiophene 93: 238042k Thiophenes, assignment of 99: 212569m Thiophenes, correlations with charge-transfer band energ. 101 : 54356t Thiophosphines 100: 34623d Thiophosphoryl chloride and its dimethylamino derivs. 79: 41554h Thiophosphoryl chloride and related cmpds. 79: 11774n Thiophosphoryl chloride derivs. 80: 102084z Thiospirane complexes 98: 169925q Thiothiophthene analogs, MO and 87: 5202y Thiourea derivs. and related heterocycles, charge distribution in relation to 91 : 73995s Thioxoketones, tautomerism in relation to 94: 156052v ethyl 78: 130011a 48

Thymine and related molecules 77: 68335h Tin 88: 128710r Tin diselenides, synchrotron radiation-excited, electronic structure in relation to 101: 219033a Tin monoxide in high temp. gas phase 97: 30800f 87: 94330d Tin tetrachloride, titanium tetrachloride and tetramethyltin 97: 63588w Titanium and titanium monoxide 101: 219064m Titanium and vanadium tetrachlorides 84: 113598d Titanium chloride and vanadium chloride 86: 197480m Titanium organometallic cmpds. 87: 167019w Titanium tetrachloride 91: 166054z Titanium tetrahalide vapors 90: 78882s 80: 87718p Toluene 77: 132734s Toluene 99: 21785u Toluene and xylene derivs. contg. trimethylsilyl grps. 90: 54084g Toluene cation, vibrational distribution in 97: 46809b Toluene, norbornadiene, cycloheptatriene, and reI. cmpds. 89: 146122a Transient and unstable species 99: 45662c Transient benzodithiete 96: 181175m Transition metal ~-methylene complexes 97: 110168w Transition metal benzenediazo complexes 86: 105650r Transition metal carbonyl cluster complexes 100: 42365m Transition metal carbonyl complexes 97: 63614b Transition metal carbonyl hydrido clusters 97: 226504g Transition metal carbonyl nitrosyls 95: 88638j Transition metal complexes with dibenzoylthioacetamide and benzoylmorpholinothiocinnamide 98: 45761p Transition metal complexes, heavy atom effect on 98: 206956y Transition metal complexes, orbital relaxation in reI. to 101: 180442f Transition metal cyclopentadienylcarbonyls 84: 67562n Transition metal cyclopentadienylcycloheptatrienyl cmpds. and related cmpds. 81: 113390t Transition metal diethylphosphorodithioato complexes 86: 81362v Transition metal difluorides 87: 46335n Transition metal dihydrides 91: 149065m Transition metal heteroligand pentacarbonyl complexes 98: 224379s Transition metal hexacarbonyls, vibrational fine struct. 96: 152029m Transition metal nitrates 93: 57640h Transition metal octahedral tris(pyrazol-l-yl)borate complexes 101: 14422e

Transition metal salt gases, SCF-Xa MO study of core .\., satellites in 97: 117699d Transition metal silicides 87: 126102z Transition metal sufamidate complexes, linkage isomerism in relation to 102: 140219c Transition metal tetracarboxylate complexes, bonding in relation to 103: 59620a Transition metal tetrafluoride oxides 94: 200362x Transition metal vapors 92: 85503p Transition metal-acetylacetone complexes 98: 169926r Transition metals 96: 152018g 49

Transition metals carbonyls, Green's function approach to 98: 24763a Transition metals chromium cyclopentadiene complexes 101 : 200122c Tri-Me and triallyl orthoformate 88: 61109b Tri-s-triazine 100: 191218t Tri-tert-butyl cyclobutadiene 82: 169626n Tri-tert-butyldimethoxyphosphorin 77: 125718m Tri-tert-butylpentalene 88: 143950n Tri-tert-butylphosphorin 76: 13353m [(Trialkylsilyl)methyl]benzenes 96: 35448m Triazine 76: 92381v sym-Triazine 103: 150101t Triazine and its Me derivs. 86: 148469f Triazines 99: 31905u Triazoles and tetrazoles, tautomerism in relation to 96: 68072n Triazoline- and thiadiazolinethiones and triazolinones 84: 42151k Tricarbonyl(cyclopentadienyl)manganese & -rhenium cmplxs. 95: 202778g Tricarbonyl(norbornadiene) iron, MO calcn. of 98: 54124k Tricarbonylmanganese complexes, electronic structure in relation to 98: 62616n (Tricyanovinyl)arylamines 84: 119840h Tricyclic 92: 21967k Tricyclic siloxane derivs. 95: 60806p Tricyclic siloxa~e derivs. 95: 60806p Tricyclo[4.2.0.0 ,5]octadienes, through-bond interactions in solvolysis in r~l~tion to 88: 151890h syn-Tricyclo[4.2.1.1 ' ]deca-3,7-dienes 89: 5988a Tricyclodecadiene deriv. 100: 156030d Tricyclododecadiene deriv. 99: 139186c Tricyclododecatetraene and bicyclooctadiene 94: 156111p Tricyclododecatetraene-contg. compd., through- bond interaction in relation to 103: 195148a Tricyclohexene, -hexane, and -heptane 86: 170184f Tricyclooctadiene 90: 86541b Tricyclooctene and tricylooctane, MO interpretation of 81 : 161128f Tricyclopentanes 100: 50110k Tricycloquinazoline 92: 93549y Tricycloundecatriene 97: 22997k Tricycloundecene and tricycloundecane alcs. and amines 98: 215061e Triethylamine, location of vibrationless second singlet state in reI. to 102 : 175124r Trifluorobenzene and trifluorobenzene-d3 18: 64651f Trifluoroethane 102 : 23965g Trifluoromethyl halo germane derivs. 96: 201819w Trifluoromethyl iodide, using synchrotron radiation 102: 102865c Trifluoromethyl isocyanide and trifluoroacetonitrile 100: 191115g Trifluoromethyl oxides and sulfide 94: 83418g Trifluorosilane derivs. 80: 65349s Trihalosilylphosphines and -arsines 88: 67586f 3,7,9-Triheterobicyclo[3.3.1]nonanes 87: 133742m Triisopropylidenecyclopropane 82: 111175y Triketones 77: 4149p Trimethyl gold phosphines 99: 38579c Trimethyl silane 98: 179615c Trimethylacetylsilane and -germane 81 : 104081x 50

Trimethylamine derivs. 81 : 151175j Trimethylamine derivs. 83: 113260s Trimethylammonium octachlorooctaoxotetraaquo- te tratungs tate 88: 82099t Trimethylene sulfite 102 : 194464x Trimethylenemethaneiron tricarbonyl and butadieneiron tricarbonyl 87: 159672p • Trimethylgermane, chlorotrimethylgermane and fluorotrimethylgermane 91: 30122n Trimethylphenyl-substituted Group IV metals 82: 85725f Trimethylsilane derivs. 76: 125955r Trimethylsilyl or tert-butyl ketones 84: 42731d {Trimethylsilyl)amidometal complexes 97: 46799y Trimethylsilylcyclohexadiene iron complexes, electronic structure in relation to 100: 156768a Trimethylsilylhaloacetylenes 77: 133005s (Trimethylsilyl)methyl and neopentyl metal complexes 78: 1100Hz (Trimethylsilyl)methyl benzene derivs. 90: 86178g Trioxonin and cyclononatriene 94: 64999f Triphenylamine cation radicals in condensed vs. vapor phases 90: 177758n Triphenylphosphine metal complexes, triphenylphosphine as internal std. for 86: 88525j Triphenylphosphines 89: 107015y Triptycene 98: 160079j Triptycenes, transannular interaction in reI. to 99: 121679f Triruthenium cmpds. with bridging hydrides 97: 182649b Tris(butadiene)molybdenum and -tungsten 97: 23952d Tris(dialkylamino)phosphines 87: 46316g Tris(dialkylamino)phosphines and diazaphospholanes 95: 33085w Tris(phenylchalcogenide)arsines and phenyldimethylarsine chalcogenides 95: 79925y Tris(trimethylindolinyl) [3.3.3]decamethinium tetrafluoroborate 99: 23997p Tris(trimethylsilyl)heptaphospanortricyclene 92: 197738a Tris(triphenylphosphine)platinum titanium tetrachloride complex 86: 170198p Tris-o-homobenzenes 92: 75602f Tris[bis{methoxyphenylimino)ethane]ruthenium 102 : 119874c Trithiapentalene, dithiaselenapentalene, and triselenapentalene 94: 83165x Tropolone and methoxytropolone and thallium tropolonate 99: 202947u Tropoquinone isomers 96: 84921u Tropyl radical 89: 23311d Tryptophan in gas phase 91: 175700j l~ Tungsten 76: 160618e Tungsten carbonyl phosphine complexes 101 : 63035q Tungsten phosphine complexes 102: 157401d ,) a,B-Unsatd. carbonyl cmpds. 94: 200379h Unsatd. 76: 7894ge Unsatd. hydrocarbons 93: 104363g Unstable dibromamine 90: 167482d Uracil 93: 104361e Uracil 82: 30547u 51

Uracil and related cmpds. 94: 14967y Uracil methyl derivs. 85: 88741f Uranium as function of wavelength, optogalvanic effect in wavelength calibration of pulsed lasers in rel. to 96: 208012v 91 : 165689y Uranium, angular distributions of electrons ejected from K-shell in 96: 60431h Uranyl salt hydrolyzates 100: 164798a Valence electrons from rare gases, angular dist. paramo 96: 226009d Vanadium cmpds. 96: 92163p Vanadocene halides, alkyls, and aryls 98: 72325f Vicinal cycloalkanetrione derivs. 84: 16424m Vinyl alc. 101 : 6418t Vinyl polymers 102: 167506f Vinyl- and alkylideneketenes 95: 114519t Vinyl- and alkylsilanes and disilanes 96: 20159u Vinylamine 101 : 6419u Vinylcyclohexene radical cation 101 : 110031 x Vinylic sulfides 84: 43088m Vinylidene anion 99: 149091g Vinylphosphonic dichloride and related cmpds. 92: 5726a Water dimer 96: 190111q Water, partial cross section and asymmetry parameters for 96: 94461h Xanthine methylated derivs. 88: 46561d Xenon 101 : 180476v Xenon 87: 143799z Xenon 84: 187250f & xenon tetrafluoride in gaseous states 88: 200597d Xenon with synChrotron radiation source, angular symmetry parameter for 98: 170007y Xenon, gngular distribution and ionization cross-section of 5p subshell in 86: 48965w Xenon, angular distribution in 86: 24199y Xenon, correlation satellites in, in region of strong interchannel interactions 101 : 100743s Xenon, elect. energy in multiphoton ionizatn. in reI. to 99: 7952ge ,Xenon, interpretation of satellites in 101 : 140456g Xenon, linewidth & branching ratio in 102 : 122504n Xenon, strong channels in satellite spectrum near Cooper min. in relation to 101 : 100683x Xenon, with synchrotron radiation source 99: 79531z Xylenes and metacyclophanes 82: 56948a o-Xylylene, low energy non-Koopmans ionization in rel. to 101 : 100753v Ytterbium, autoionization decay in relation to 101 : 14455t

') This report was done with support from the Department of Energy. Any conclusions or opinions expressed in this report represent solely those of the author(s) and not necessarily those of The Regents of the University of California, the Lawrence Berkeley Laboratory or the Department of Energy. Reference to a company or product name does not imply approval or recommendation of the product by the University of California or the U.S. Department of Energy to the exclusion of others that may be suitable. -\, _;a _,. ...."'...... --t~.

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