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Lawrence Berkeley National Laboratory Recent Work Title REFERENCES TO ULTRAVIOLET PHOTOELECTRON SPECTRA OF GASEOUS MOLECULES Permalink https://escholarship.org/uc/item/3bf9869z Authors Horne, D.H. Jolly, W.L. Publication Date 1986-09-01 eScholarship.org Powered by the California Digital Library University of California DISCLAIMER 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 Acetaldehyde and acetyl halides, MO interpretn. of 80: 76412h Acetaldehyde and ethylene oxide 97: 197664b Acetaldehyde and methyl ketones 81 : 2965q Acetaldehyde, acetone, and iodine vapors, spectral dependence of slow-photoelectron generation in 86: 180259y Acetaldehyde, deuterium shifts in 84: 179100s Acetals 96: 51524p Acetanilides and oxindole 93: 131966n Acetanilides, steric and inductive effects in 83: 77933c Acetic acid and trifluoroacetic acid monomers & dimers 93: 84571t Acetic and formic acid 91 : 55907k Acetone 87: 200467r Acetone derivs. 102 : 5518j Acetone ions and dimethylmercury ions 83: 27113q Acetonitrile 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 Acetylene 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 nitrogen 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, carbon monoxide, and xenon, threshold 91 : 131730q Acetylenes and methylacetylenes 80: 26425u Acetylenes and vinylacetylenes contg. Group IV elements 97: 92452c Acrole·in 92: 67357q Actinide 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. hydrocarbons 86: 71185a Aliph. hydrocarbons and tetramethylsilane, solid-vapor threshold ionizatn. potentials in relation to 99: 130895a Alk. chlorides and iodides at high temp., 88: 143959x Alk. earth fluoride 81 : 18823c Alk. earth fluorides, uv and x-ray 84: 67555n Alk. earth halides 88: 97129b Alk. earth halides 90: 194806u Alkadiynes, radical cations in 92: 75507d Alkali halide monomers, dimers and trimers 96: 152060q Alkali iod ides 101 : 200707b Alkali metaborate vapors 93: 84570s Alkali metal cyanides & 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 oxides 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, acrylonitrile & 3-butenenitrile 100: 42314u Alkanes 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 alkane radical cations in relation to 103 : 141374g Alkanes, silanes and methylsilanes, vs. MO calcns. 99: 175862d Alkene and cycloalkene ozonides 89: 214534p (Alkene)iron tetracarbonyl cmpds. 91 : 131712k Alkenes, cycloalkenes, and methylene cycloalkanes 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 sulfides, sulfoxides and sulfones, conformation in relation to 95: 6339a Alkyl aryl ethers and sulfides, conformation in reI. to 82: 57415m Alkyl aryl selenides 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 peroxides 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 diacetylene 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 benzenes 87: 133520n Alkyltin cmpds. 89: 23320f Alkyne iron cluster complexes 98: 107487q Alkynes 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 propyne 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 azide 100: 156743p Allyl halides 81 : 8152u Allyl halides and vinyl halides 79: 110101x Allyl iron cobalt complexes 96: 218006k Allyl methyl sulfide & methyl sulfide, carbon-sulfur bonding in relation to 77: 95168n Allyl thiol, 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 bismuth
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  • Standard Thermodynamic Properties of Chemical

    Standard Thermodynamic Properties of Chemical

    STANDARD THERMODYNAMIC PROPERTIES OF CHEMICAL SUBSTANCES ∆ ° –1 ∆ ° –1 ° –1 –1 –1 –1 Molecular fH /kJ mol fG /kJ mol S /J mol K Cp/J mol K formula Name Crys. Liq. Gas Crys. Liq. Gas Crys. Liq. Gas Crys. Liq. Gas Ac Actinium 0.0 406.0 366.0 56.5 188.1 27.2 20.8 Ag Silver 0.0 284.9 246.0 42.6 173.0 25.4 20.8 AgBr Silver(I) bromide -100.4 -96.9 107.1 52.4 AgBrO3 Silver(I) bromate -10.5 71.3 151.9 AgCl Silver(I) chloride -127.0 -109.8 96.3 50.8 AgClO3 Silver(I) chlorate -30.3 64.5 142.0 AgClO4 Silver(I) perchlorate -31.1 AgF Silver(I) fluoride -204.6 AgF2 Silver(II) fluoride -360.0 AgI Silver(I) iodide -61.8 -66.2 115.5 56.8 AgIO3 Silver(I) iodate -171.1 -93.7 149.4 102.9 AgNO3 Silver(I) nitrate -124.4 -33.4 140.9 93.1 Ag2 Disilver 410.0 358.8 257.1 37.0 Ag2CrO4 Silver(I) chromate -731.7 -641.8 217.6 142.3 Ag2O Silver(I) oxide -31.1 -11.2 121.3 65.9 Ag2O2 Silver(II) oxide -24.3 27.6 117.0 88.0 Ag2O3 Silver(III) oxide 33.9 121.4 100.0 Ag2O4S Silver(I) sulfate -715.9 -618.4 200.4 131.4 Ag2S Silver(I) sulfide (argentite) -32.6 -40.7 144.0 76.5 Al Aluminum 0.0 330.0 289.4 28.3 164.6 24.4 21.4 AlB3H12 Aluminum borohydride -16.3 13.0 145.0 147.0 289.1 379.2 194.6 AlBr Aluminum monobromide -4.0 -42.0 239.5 35.6 AlBr3 Aluminum tribromide -527.2 -425.1 180.2 100.6 AlCl Aluminum monochloride -47.7 -74.1 228.1 35.0 AlCl2 Aluminum dichloride -331.0 AlCl3 Aluminum trichloride -704.2 -583.2 -628.8 109.3 91.1 AlF Aluminum monofluoride -258.2 -283.7 215.0 31.9 AlF3 Aluminum trifluoride -1510.4 -1204.6 -1431.1 -1188.2 66.5 277.1 75.1 62.6 AlF4Na Sodium tetrafluoroaluminate
  • Durham E-Theses

    Durham E-Theses

    Durham E-Theses Methtleneamino-derivatives of some transition metal carbonyls Midcalf, Christopher How to cite: Midcalf, Christopher (1971) Methtleneamino-derivatives of some transition metal carbonyls, Durham theses, Durham University. Available at Durham E-Theses Online: http://etheses.dur.ac.uk/8649/ Use policy The full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-prot purposes provided that: • a full bibliographic reference is made to the original source • a link is made to the metadata record in Durham E-Theses • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders. Please consult the full Durham E-Theses policy for further details. Academic Support Oce, Durham University, University Oce, Old Elvet, Durham DH1 3HP e-mail: [email protected] Tel: +44 0191 334 6107 http://etheses.dur.ac.uk METHYLENEAMINO- DERTVATIVE S OF SOME TRANSITION METAL CARBONYLS by Christopher Midcalf, B.Sc. A thesis submitted to the University of Durham for the degree of Doctor of Philosophy July 1971 MEMORANDUM The work described in this thesis was carried out in the University of Durham between October 1968 and July 1971. It has not been submitted for any other degree and is the original work of the author except when acknowledged by reference. Part of the work in this thesis has formed the subject matter of the following publications: (i) Unsaturated Organonitrogen Groups in Carbonyl Complexes of Molybdenum, Tungsten and Manganese.