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Use of Bismuth Compounds for the Manufacture of Medicaments for The
Europäisches Patentamt *EP000805815B1* (19) European Patent Office Office européen des brevets (11) EP 0 805 815 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.7: A61K 33/24, C07F 9/94, of the grant of the patent: A61K 49/04 10.04.2002 Bulletin 2002/15 (86) International application number: (21) Application number: 96901066.9 PCT/GB96/00183 (22) Date of filing: 26.01.1996 (87) International publication number: WO 96/22994 (01.08.1996 Gazette 1996/35) (54) Use of bismuth compounds for the manufacture of medicaments for the treatment of gastric disorders caused by Helicobacter pylori Verwendung von WISMUTVERBINDUNGEN zur Herstellung eines Arzneimittels zur Behandlung von Magenverstimmungen, die durch Helicobacter pylori verursacht werden Utilisation de COMPOSES DE BISMUTH pour la fabrication de médicaments pour le traitement de troubles gastriques associées avec Helicobacter pylori (84) Designated Contracting States: EP-A- 0 480 691 EP-A- 0 716 091 DE DK ES FR GB IE IT SE WO-A-91/03241 WO-A-93/02713 WO-A-95/06053 WO-A-96/16677 (30) Priority: 26.01.1995 GB 9501560 WO-A-96/16678 BE-A- 782 105 07.06.1995 US 486225 DE-A- 2 216 725 (43) Date of publication of application: • TETRAHEDRON LETT. (TELEAY,00404039);94; 12.11.1997 Bulletin 1997/46 VOL.35 (44); PP.8197-200, KYOTO UNIV.;FAC. SCI.; KYOTO; 606-01; JAPAN (JP), SUZUKI H ET (73) Proprietor: NYCOMED IMAGING A/S AL ’Ultrasonic reaction of triarylbismuthines 0401 Oslo (NO) and triarylstibines with iodosylbenzene. Mild oxidizing ability of the organobismuth oxide (72) Inventors: function for organic substrates’ • KLAVENESS, Jo • DATABASE CHEMABS CHEMICAL ABSTRACTS N-1166 Oslo (NO) SERVICE, COLUMBUS, OHIO, US ASTHANA A • BERG, Arne ’Reactions of triphenyl antimony, bismuth and N-1300 Sandvika (NO) their dibromides with pentachlorophenol and • ALMEN, Torsten pentachlorothiophenol’ & INDIAN J. -
United States Patent (19) ’11) 4,095,037 Stapp 45) June 13, 1978
United States Patent (19) ’11) 4,095,037 Stapp 45) June 13, 1978 54 METHOD FOR THE oxIDATION OF A 56) References Cited CONJUGATED DOLEFN U.S. PATENT DOCUMENTS 3,238,225 3/1966 Brill................................ 260/346.1 (75) Inventor: Paul R. Stapp, Bartlesville, Okla. 3,432,558 3/1969 Ryland ................................. 260/604 3,670,014 6/1972 Fernholz .......................... 260/497 A 73 Assignee: Phillips Petroleum Company, 3,755,423 8/1973 Onoda .............................. 260/497 A. Bartlesville, Okla. 3,922,300 11/1975 Onoda .............................. 260/497. A Primary Examiner-James O. Thomas, Jr. 21 Appl. No.: 721,645 Assistant Examiner-Michael Shippen 22 Filed: Sep. 8, 1976 57 ABSTRACT A conjugated diolefin is reacted with a carboxylic acid, (51) Int, C.’......................... CO7C 67/05; B01J 23/16 a carboxylic acid anhydride, or a mixture thereof, in the (52) U.S.C. .................................... 560/246; 260/410; presence of oxygen and a catalyst comprising a com 260/410.6; 260/465.4; 560/1; 560/106; pound of bismuth, an alkali metal compound and a 560/112; 560/122; 560/228; 560/230; 252/438 source of nitrate ion. 58 Field of Search ........... 260/497 R, 497 A, 476 R, 260/410, 40.6, 465.4, 468 R, 487 11 Claims, No Drawings 4,095,037 1. METHOD FOR THE OXDATION OF A . R. R. R. 1) CONJUGATED DOLEFN C-CEC as R. BACKGROUND OF THE INVENTION The invention relates to a method suitable for the In said formula (1), R- is selected from the group oxidation of a conjugated diolefin. In another aspect, consisting of H-, F-, CL-, Br-, -, -CsN, the invention relates to a composition useful as a cata lyst. -
United States Patent (19) 11 Patent Number: 6,117,412 Klaveness Et Al
USOO6117412A United States Patent (19) 11 Patent Number: 6,117,412 Klaveness et al. (45) Date of Patent: *Sep. 12, 2000 54) NON-CLUSTER TYPE BISMUTH 5,417,958 5/1995 Deutsch et al. ........................ 424/9.42 COMPOUNDS 5,482,669 1/1996 Shah. 5,482,700 1/1996 Deutsch et al.. 75 Inventors: Jo Klaveness, Oslo; Ame Berg, 5,730,953 3/1998 Suzuki et al. .......................... 424/9.42 Sandvika, both of Norway; Torsten 5,817,289 10/1998 Klaveness et al. .................... 424/1.11 Almen, Falstorbo, Sweden; Klaes FOREIGN PATENT DOCUMENTS Golman, Rungsted Kyst, Denmark; 809388 5/1974 Belgium. Michael Droege, Livermore; Shi-bao O O217 577 Yu, Campbell, both of Calif. A2 9/1986 European Pat. Off.. O 230 893 A2 1/1987 European Pat. Off.. 73 Assignee: Nycomed Imaging AS, Norway O 445 743 A2 9/1991 European Pat. Off.. 0 480 691 A2 4/1992 European Pat. Off.. * Notice: This patent is Subject to a terminal dis O OS33 281 claimer. A1 9/1992 European Pat. Off.. 0 716 091 A1 8/1994 European Pat. Off.. 21 Appl. No.: 08/875,305 2216725 10/1973 Germany. 63-225381 9/1988 Japan. 22 PCT Filed: Jan. 26, 1996 81/7456 4/1983 South Africa. 86 PCT No.: PCT/GB9600183 1003685 9/1965 United Kingdom. 1341331 12/1973 United Kingdom. S371 Date: Oct. 22, 1997 2 248 185 1/1992 United Kingdom. 2 262 036 6/1993 United Kingdom. S 102(e) Date: Oct. 22, 1997 WO 89/00557 1/1989 WIPO. WO 89/03219 4/1989 WIPO. -
5.157 TABLE 5.29 Van Der Waals' Constants for Gases the Van Der
DEAN #37261 (McGHP) RIGHT INTERACTIVE top of rh PHYSICAL PROPERTIES 5.157 base of rh cap height TABLE 5.29 Van der Waals’ Constants for Gases base of text The van der Waals’ equation of state for a real gas is: na2 ͩͪP ϩ (V Ϫ nb) ϭ nRT for n moles V2 where P is the pressure, V the volume (in liters per mole ϭ 0.001 m3 per mole in the SI system), T the temperature (in degrees Kelvin), n the amount of substance (in moles), and R the gas constant. To use the values of a and b in the table, P must be expressed in the same units as in the gas constant. Thus, the pressure of a standard atmosphere may be expressed in the SI system as follows: 1 atm ϭ 101,325 N · mϪ2 ϭ 101,325 Pa ϭ 1.01325 bar The appropriate value for the gas constant is: 0.083 144 1 L · bar · KϪ1 · molϪ1 or 0.082 056 L · atm · KϪ1 · molϪ1 The van der Waals’ constants are related to the critical temperature and pressure, tc and Pc, in Table 6.5 by: 27 RT22 RT a ϭ ccand b ϭ 64 Pcc8 P Substance a,L2 · bar · molϪ2 b,L·molϪ1 Acetaldehyde 11.37 0.08695 Acetic acid 17.71 0.1065 Acetic anhydride 26.8 0.157 Acetone 16.02 0.1124 Acetonitrile 17.89 0.1169 Acetyl chloride 12.80 0.08979 Acetylene 4.516 0.05218 Acrylic acid 19.45 0.1127 Acrylonitrile 18.37 0.1222 Allene 8.235 0.07467 Allyl alcohol 15.17 0.1036 Aluminum trichloride 42.63 0.2450 2-Aminoethanol 7.616 0.0431 Ammonia 4.225 0.03713 Ammonium chloride 2.380 0.00734 Aniline 29.14 0.1486 Antimony tribromide 42.08 0.1658 Argon 1.355 0.03201 Arsenic trichloride 17.23 0.1039 Arsine 6.327 0.06048 Benzaldehyde 30.30 0.1553 Benzene 18.82 -
(12) United States Patent (10) Patent No.: US 6,596,206 B2 Lee (45) Date of Patent: *Jul
USOO6596206B2 (12) United States Patent (10) Patent No.: US 6,596,206 B2 Lee (45) Date of Patent: *Jul. 22, 2003 (54) GENERATION OF PHARMACEUTICAL FOREIGN PATENT DOCUMENTS AENESSING FOCUSED WO WO OO/37169O542314 6/20007/1998 (75) Inventor: partson-Hui Lee, Mountain View, W W s: 2: OTHER PUBLICATIONS (73) Assignee: Picoliter Inc., Sunnyvale, CA (US) Debenedetti et al. (1993), “Application of Supercritical Fluids for the Production of Sustained Delivery Devices.” (*) Notice: Subject to any disclaimer, the term of this Journal of Controlled Release 24:27–44. patent is extended or adjusted under 35 Tom et al. (1991), “Formation of Bioerodible Polymeric U.S.C. 154(b) by 14 days. Microspheres and Microparticles by Rapid Expansion of Supercritical Solutions,” Biotechnol. Prog. 7(5):403-411. This patent is Subject to a terminal dis- Chattopadhyay et al. (2001), “Production of Griseofulvin claimer. Nanoparticles Using Supercritical CO2 Antisolvent with Enhanced Mass Transfer.” International Journal of Phar (21) Appl. No.: 09/823,899 maceutics 228:19-31. (22) Filed: Mar 30, 2001 Jung et al. (2001), “Particle Design Using Supercritical e a Vs Fluids: Literature and Patent Survey,” Journal of Supercriti (65) Prior Publication Data cal Fluids 20:179-219. Primary Examiner Mary Lynn Theisen US 2002/0142049 A1 Oct. 3, 2002 (74) Attorney, Agent, or Firm-Dianne E. Reed; Reed & (51) Int. Cl." .................................................. B29C 9/00 Eberle LLP (52) U.S. Cl. ....................... 264/9; 264/5; 2647. (57) ABSTRACT (58) Field of Search ......................... 264/9, 7, 5; 425/6, A method and device for generating pharmaceutical agent 425/10 particles using focused acoustic energy are provided. -
The Radiochemistry of Bismuth
NAS-NS-3061 RA OFBISMUTH NUCLEAR SCIENCE SERIES National Academy of Sciences - National Research Council Published by Technical Information Center ENERGY RESEARCH AND DEVELOPMENT ADMINISTRATION COMMITTEE ON NUCLEAR SCIENCE John Huizenga, Chairman, Nuclear WrUcture Re=arch Laboratory Thomas A. Tombrello, Vice Chairman, California institute of T=hnology C. K. Reed, Executive Secretary,Netional Academy of Sciences Lowell M. Bollinger, Argonne Nationel Laboratow Peggy Dyer, UnivarsiW of Washington Rusaall Heath, Aerojet Nuclear Co., Inc. Roy K. Middlaton, University of Pennsylvania 1: Lon Morgan, Columbie Scientific Industries G. Davis O’Kelley, Oek Ridge National Laboratow G. C. Phillips, Rice University Henry N. Wagner, Jr., The Johns Hopkins Medial Institutions Joseph Wen~, Brookhaven National Laboratory Sheldon’ Wolff, University of California Chien-Shiung Wu, Columbia Univar?@ Alexander Zuckar, Oak Ridga National Laborato~ Liaison Members William S. Rodney, National science Foundation George L. ROWS, Energy Research and Development Admini-ration SUBCOMMITTEE ON RAD1OCHEMISTRY G. Davis O’Kelley, Chairmsrr, Oak Ridge National Laboratory Glen E. Gordon, UnivwsiW of Maryler& ‘“- ,-. Rolfa H. Hw*r, Rutgers Univemity John A. Miskel, Lawrence Livermore LaboratoW Harold A. O’Brien, Jr., Los Alamos Scientific Laboratory Richard W. Perkins. Bettafle Pacific Northwest Laboratories Andrew F. Stehney, Argonne National Laboratory Kurt Wotfsbarg, Los Alanros Scientific Laboratow LiaisonMembers ~ John L. Burnatte, Energy Research and Davelopmant Administration FTed Findeis, National Scienca Foundation i.,.~.. Radiochemistry of Bismuth Kashinath S. Bhatki Tata Instituteof Fundamental Research Homi Bhabha Road, Bombay 400005 and Bhabha Atomic ResearchC-entre Trornbay,Bombay 400085 (India) Prepared for Subcommittee on Radiochemistry National Academy of Sciences - Natiorial Research Council IssuanceDate:September 1977 Published by Technical 1nform,ation center ENERGY RESEARCH AND DEVELOPMENT ADMINISTRATION Price$4.75.Availablefrom: NationalTechnicalInformationservice U. -
Semiconductive Coordination Networks from Bismuth(III) Bromide and 1,2-Bis(Methylthio)Phenylacetylene-Based Ligands
Inorg. Chem. XXXX, XX, Semiconductive Coordination Networks from Bismuth(III) Bromide and 1,2-Bis(methylthio)phenylacetylene-Based Ligands Kunhao Li,† Hanhui Xu,† Zhengtao Xu,*,†,‡ Matthias Zeller,§ and Allen D. Hunter§ Department of Chemistry, the George Washington UniVersity, 725 21st Street NW, Washington, D.C. 20052, Department of Biology and Chemistry, City UniVersity of Hong Kong, 83 Tat Chee AVenue, Kowloon, Hong Kong, P. R. China, and Department of Chemistry, Youngstown State UniVersity, 1 UniVersity Plaza, Youngstown, Ohio 44555 Received July 28, 2005 This paper reports our initial efforts to integrate phenylacetylene-based conjugate π-electron systems into hybrid semiconductive coordination networks, as part of the larger scheme to fully synergize organic functionalities and electronic properties in crystalline solid-state materials. On the basis of a well-established Pd-catalyzed procedure, ligands of 3,3′,4,4′-tetrakis(methylthio)tolan (L1) and 1,3,5-tris{[3,4-bis(methylthio)phenyl]ethynyl}benzene (L2) were efficiently synthesized in relatively simple procedures. Molecule L1 reacts with BiBr3 to form a 2D semiconductive coordination network (L1‚2BiBr3), which consists of infinite chains of the BiBr3 component cross-linked by L1 through the chelation between the 1,2-bis(methylthio) groups and the Bi(III) centers. Molecule L2 reacts with BiBr3 to from a 1D semiconductive coordination network (L2‚2BiBr3), which features discrete tetrameric Bi4Br12 units linked by the thioether groups from L2 [only two of the three 1,2-bis(methylthio) groups from each L2 molecule are bonded to the Bi(III) centers]. Diffuse reflectance spectra of both L1‚2BiBr3 and L2‚2BiBr3 feature strong optical absorptions at energy levels significantly lower than those of the corresponding molecular solids (L1 and L2) and BiBr3, indicating significant electronic interaction between the organic π-electron systems and the BiBr3 components. -
Convenient, Bismuth Mediated, One-Pot, Two Component Synthesis of 2,6-Disubstituted-3,4-Dihydropyrans
W&M ScholarWorks Undergraduate Honors Theses Theses, Dissertations, & Master Projects 5-2011 Convenient, Bismuth Mediated, One-pot, Two Component Synthesis of 2,6-Disubstituted-3,4-Dihydropyrans Robert Frederick Lambert College of William and Mary Follow this and additional works at: https://scholarworks.wm.edu/honorstheses Part of the Chemistry Commons Recommended Citation Lambert, Robert Frederick, "Convenient, Bismuth Mediated, One-pot, Two Component Synthesis of 2,6-Disubstituted-3,4-Dihydropyrans" (2011). Undergraduate Honors Theses. Paper 371. https://scholarworks.wm.edu/honorstheses/371 This Honors Thesis is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Undergraduate Honors Theses by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. Convenient, Bismuth Mediated, One-pot, Two Component Synthesis of 2,6- Disubstituted-3,4-Dihydropyrans A thesis submitted in partial fulfillment of the requirement for the degree of Bachelor of Science with Honors in Chemistry from the College of William and Mary in Virginia, by Robert Frederick Lambert May, 2011 Accepted for_____________________ _________________________________ Robert J. Hinkle, Director, Chemistry _________________________________ Lisa M. Landino, Chemistry _________________________________ Julie G. Galambush, Religious Studies Williamsburg, VA May 3, 2011 Table of Contents Abstract……………………………………………………………………………1 List of Figures……………………………………………………………………..2 -
The Bismuth Bromido Clusters In
Main Group Met. Chem. 2014; 37(5-6): 119–124 Katarzyna Wójcik, Ana Maria Preda, Tobias Rüffer, Heinrich Lang and Michael Mehring* Two in one: the bismuth bromido clusters * in [Bi6Cp 6Br9][Bi7Br24] * 4- Abstract: The reaction of [FeCp (CO)2]2 in CH2Cl2 with BiBr3 [Bi4Br16] (Norman, 1998). Diverse cations were used to + in a 1:1 molar ratio gave the novel bismuth compound stabilize such bromido bismuthates, e.g., [Ph4P] (Ahmed * + + [Bi6Cp 6Br9][Bi7Br24] (1), which is composed of a cationic et al., 2001a,b), [Me3HP] (Clegg et al., 1991), [Me2NH2] , + 5 + and an anionic bismuth bromido cluster: the cation is [Et2NH2] , and even [Fe(η -C5H5)2] (Norman, 1998). based on a hexanuclear bismuth {Bi6}-octahedron and the We report on the synthesis and structure of * 3- anion showing the first heptanuclear bismuth-bromido [Bi6Cp 6Br9][Bi7Br24] (1), containing heptanuclear [Bi7Br24] , cluster within the class of bromido bismuthates. which is not reported for bismuth bromido complexes. The iodide analog was only recently described by Monakhov Keywords: crystal structure; bismuth bromide; penta- et al. as anionic part of the crystal structure of [Bi(OAc)2 methylcyclopentadienyl; polynuclear clusters. (thf)4]3[Bi7I24], which was obtained by the reaction of BiI3 with [Pd(OAc)2] (Monakhov et al., 2012). However, the first report on [Bi I ]3- dates back to 1996, but details on syn- DOI 10.1515/mgmc-2014-0036 7 24 Received September 29, 2014; accepted October 22, 2014 thesis and structure were not given (Carmalt et al., 1996). In addition to the anionic cluster in 1, a cationic bismuth complex with Cp*Bi moieties is observed in the solid state. -
Structrural Peculiarities and Some Electrical-And-Physical Properties of Bismuth Oxide and Antimony Trichloride and Tribromide
240 Nanomaterials: Applications and Properties (NAP-2011). Vol. 1, Part I STRUCTRURAL PECULIARITIES AND SOME ELECTRICAL-AND-PHYSICAL PROPERTIES OF BISMUTH OXIDE AND ANTIMONY TRICHLORIDE AND TRIBROMIDE Kurban R. Kurbanov, Natalya N. Kurbanova KNUAP, Lenina 59a, 100012, Karaganda, Kazakhstan ABSTRACT The systems of antimony oxide (III) – antimony chloride (III), antimony oxide (III) – antimony bromide ɛɪɨɦɢɞ (III), bismuth oxide (III) – bismuth chloride (III) and bismuth oxide (III) – bismuth bromide (III) are the sections of the triple systems metal - oxygen - halogen. In the present report there is considered the information found in literature of the phase diagrams of binary systems components: metal – oxygen, metal – halogen – and literature data of methods of obtaining, structures and properties of the compounds in the systems. The analysis of the elementary cells parameters permitted to suppose their laminated structure and to build these compounds structures models. By the NQR method there was established the absence of the inversion center in some bismuth oxo-halogenides (by the presence of piezoelectric resonance lines) and revealed a significant dependence of NQR spectra transitions intensity on weak magnetic fields. From the practical point of view the interest presents further studying of crystal structures and physical properties of some bismuth oxo-halogenides, as due to the defect oxygen sublattice they can appear to be efficient solid electrolytes. INTRODUCTION For the first time crystal structure of Į – Bi2O3 modification was defined by Sillen [1, 2] according to Weisenberg’s X-ray photographs. Bismuth atoms position were defined from the analysis of interatom function of Paterson and of oxygen atoms – from space considerations. Repeated studies confirmed the positions of the two oxygen atoms and verified the position of the third oxygen atom [3, 4]. -
Flame Retardant Concentrates and Process for Their Preparation
Europaisches Patentamt European Patent Office © Publication number: 0 482 600 A2 Office europeen des brevets EUROPEAN PATENT APPLICATION © Application number: 91118055.2 int. Ci.5; C08K 5/16, C08L 23/02 @ Date of filing: 23.10.91 ® Priority: 23.10.90 IT 2183790 © Applicant: Himont Incorporated 2801 Centerville Road @ Date of publication of application: New Castle County Delaware(US) 29.04.92 Bulletin 92/18 @ Inventor: Bertelli, Guido © Designated Contracting States: 56, Via R. Angelini AT BE CH DE DK FR GB IT LI NL SE 1-44100 Ferrara(IT) Inventor: Goberti, Paolo 53, Via Fondo Reno I-44049 Vigarano Mainarda, Ferrara(IT) © Representative: Zumstein, Fritz, Dr. et al Dr. F. Zumstein Dipl.-lng. F. Klingseisen Brauhausstrasse 4 W-8000 Munchen 2(DE) © Flame retardant concentrates and process for their preparation. © Concentrate of a flame retardant additive, in the form of nonextruded particles, each one comprising: A) a matrix of a nonextruded, as polymerized particle, preferably spheroidal, of a polymer or copolymer of olefins having porosity greater than or equal to 15%, expressed as a percent of the void volume on the total volume of the particle, B) the product of reaction between bismuth or antimony trichloride or tribromide, or their mixtures, and one or more amines; wherein said product (B) is made "in situ" and deposited on the surface of the matrix and inside the pores thereof. CM CO CM 00 Rank Xerox (UK) Business Services [-12. 17/2.0) EP 0 482 600 A2 The present invention relates to nonextruded concentrates of a flame retardant additive, which can be used in the manufacture of polymers, and in particular of polyolefins, and the process for their preparation. -
Molecular Structures of Gas-Phase Polyatomic Molecules Determined by Spectroscopic Methods
Molecular Structures of Gas-Phase Polyatomic Molecules Determined by Spectroscopic Methods Marlin D. Harmony Department of Cherni..str)', The University of Kansas, Lawrence, KS 66045 Victor W. Laurie Department of Chemistry, Princeton Unit'er.it)", Princeton, NJ 08540 Robert L. Kuczkowski Department of Chemistry, University of Michigan, Ann Arbor, Ml48109 R. H. Schwendeman Department of Chemistry, Michigan State University, East Lansing, MI 48824 D. A. Ramsay Her::;berg institute of Astrophysics, National Research COl/neil of Canada, OIlf1l<'U, KIA ORG, Canada Frank J. Lovas, Walter J. Lafferty, and Arthur G. Maki National Bureau of Standards, Washing/Oil, DC 20334 Spectroscopic data related to the structures of polyatomic molecules in the gas phase have been reviewed, critically evaluated, and compiled. All reported bond distances and angles have been classified as equilibrium (r 0)' average (r,), substitution (r.), or effective (ro) parameters, and have been given a quality rating which is a measure of the parameter uncertainty. The surveyed literature includes work from all of the areas of gas-phase spectroscopy from which precise quantitative struc· tural information can be derived. Introductory material includes definitions of the various types of parameters and a description of the evaluation procedure. Key words: Bond angles; bond distances; gas·phase polyatomic molecules; gas·phase spectroscopy; microwave spectroscopy; molecular conformation; molecular spectroscopy; molecular structure; molecules; SLrUClure. Contents Page Page 1. Introduction.... .. ............. 619 Inorganic Molecules ....................... 628 2. Definitions of Structural Parameters ......... 620 C1 Molecules ............................. 650 3. Uncertainties ............................ 623 C~ Molecules ............................. 668 4,. Evaluation Procedure ..................... 625 C3 Molecules ............................. 688 5. Description of Tables ..................... 625 c.! Molecules ............................. 702 Appendix: Selected Diatomic Molecule Distances .