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  <doc>
    <id>56998</id>
    <completedYear/>
    <publishedYear>1995</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>768</pageFirst>
    <pageLast>770</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>51</volume>
    <type>article</type>
    <publisherName>Wiley-Blackwell</publisherName>
    <publisherPlace>Oxford</publisherPlace>
    <creatingCorporation>International Union of Crystallography</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">(Carboxymethyl)dimethylundecylammonium bromide</title>
    <abstract language="eng">The title compound, C₁₅H₃₂NO₂⁺.Br⁻, crystallizes to form layers with interdigitating hydrocarbon chains stabilized by Br⁻۰۰۰H—O hydrogen bonds and Br⁻۰۰۰N⁺ contacts.</abstract>
    <parentTitle language="eng">Acta crystallographica - Section C</parentTitle>
    <identifier type="issn">0108-2701</identifier>
    <identifier type="doi">10.1107/s0108270194011443</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="date_peer_review">31.12.2015</enrichment>
    <author>R. Rudert</author>
    <author>Burkhard Schulz</author>
    <author>Günter Reck</author>
    <author>D. Vollhardt</author>
    <author>J. Kriwanek</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>(Carboxymethyl)dimethylundecylammonium bromide</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Crystal structure</value>
    </subject>
    <collection role="ddc" number="543">Analytische Chemie</collection>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
  <doc>
    <id>61831</id>
    <completedYear/>
    <publishedYear>1999</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1179</pageFirst>
    <pageLast>1193</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>130</volume>
    <type>article</type>
    <publisherName>Springer</publisherName>
    <publisherPlace>Wien</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Thermal behaviour and crystal structure of sodium-containing hemihydrates of calcium sulfate</title>
    <abstract language="eng">A metastable sodium-containing hemihydrate ((6-x)CaSO₄∙xNa₂SO₄∙3H₂O, 0≤x≤1) limited by the pentasalt composition Na₂SO₄∙5CaSO₄∙3H₂O occurs as an intermediate solid phase in the systems Na₂SO₄-CaSO₄-H₂O, NaCl-Na₂SO₄-CaSO₄-H₂O, and NaCl-CaSO₄-H₂O. X-Ray structure determination of a crystal with pentasalt composition results in a super-structure of the pure hemihydrate (CaSO₄∙0.5H₂O), in which one Ca²⁺ion is statistically replaced by two Na⁺ ions. One Na⁺ cation is situated in a Ca²⁺ position in only one of the three chains of CaSO₄ forming an axis of nearly three fold symmetry along the c-axis. The second Na⁺ is located in the water channel neighbouring to the first Na⁺. The hydrate crystallized in a monoclinic space group C121 (No. 5) with a=24.1781(11), b=13.805(2), c=12.7074(12) Å, β=90.089(12)°. The dehydration temperature of the hydrates depends on their Na⁺ ion content. A high Na⁺ content (in water channels) blocks the water escape strongly, and the dehydration temperature increases. Thermal behaviour is also effected by the crystal sizes. The thermograms of small crystals as opposed to large ones show a exothermic effect adjoining the endothermic dehydration. This may be indicative for a change in the dehydration mechanism upon crystal size.</abstract>
    <parentTitle language="eng">Monatshefte für Chemie = Chemical Monthly</parentTitle>
    <identifier type="issn">1434-4475</identifier>
    <identifier type="doi">10.1007/pl00010180</identifier>
    <identifier type="issn">0026-9247</identifier>
    <enrichment key="opus_doi_flag">true</enrichment>
    <enrichment key="opus_import_data">{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,2]],"date-time":"2022-04-02T13:34:29Z","timestamp":1648906469773},"reference-count":0,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[1999,10,1]],"date-time":"1999-10-01T00:00:00Z","timestamp":938736000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Monatshefte fuer Chemie"],"published-print":{"date-parts":[[1999,10]]},"DOI":"10.1007\/pl00010180","type":"journal-article","created":{"date-parts":[[2006,2,17]],"date-time":"2006-02-17T12:03:04Z","timestamp":1140177784000},"page":"1179-1193","source":"Crossref","is-referenced-by-count":0,"title":["Thermal Behaviour and Crystal Structure of Sodium-Containing Hemihydrates of Calcium Sulfate"],"prefix":"10.1007","volume":"130","author":[{"given":"Daniela","family":"Freyer","sequence":"first","affiliation":[]},{"given":"G\u00fcnter","family":"Reck","sequence":"additional","affiliation":[]},{"given":"Martina","family":"Bremer","sequence":"additional","affiliation":[]},{"given":"Wolfgang","family":"Voigt","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[1999,10,1]]},"container-title":["Monatshefte f\u00fcr Chemie \/ Chemical Monthly"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/PL00010180.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/PL00010180\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/PL00010180","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,22]],"date-time":"2019-05-22T22:01:24Z","timestamp":1558562484000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/PL00010180"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1999,10]]},"references-count":0,"journal-issue":{"issue":"10","published-print":{"date-parts":[[1999,10]]}},"alternative-id":["91301179"],"URL":"http:\/\/dx.doi.org\/10.1007\/pl00010180","relation":{},"ISSN":["0026-9247","1434-4475"],"issn-type":[{"value":"0026-9247","type":"print"},{"value":"1434-4475","type":"electronic"}],"subject":[],"published":{"date-parts":[[1999,10]]}}}</enrichment>
    <enrichment key="local_crossrefDocumentType">journal-article</enrichment>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="date_peer_review">09.03.2012</enrichment>
    <enrichment key="opus.doi.autoCreate">false</enrichment>
    <enrichment key="opus.urn.autoCreate">true</enrichment>
    <author>D. Freyer</author>
    <author>Günter Reck</author>
    <author>M. Bremer</author>
    <author>W. Voigt</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Bassanite</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Crystal structure</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Sodium pentasalt</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Calcium sulfate hemihydrate</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Thermal analysis</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
  <doc>
    <id>44409</id>
    <completedYear/>
    <publishedYear>1995</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1476</pageFirst>
    <pageLast>1479</pageLast>
    <pageNumber/>
    <edition/>
    <issue>5203</issue>
    <volume>267</volume>
    <type>article</type>
    <publisherName>AAAS, American Association for the Advancement of Science</publisherName>
    <publisherPlace>Washington, DC</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">A "double-diamond superlattice" built up of Cd17S4(SCH2CH20H)26 clusters</title>
    <abstract language="eng">A simple preparation of Cd17S4(SCH2CH2OH)26 clusters in aqueous solution leads to the formation of colorless blocky crystals. X-ray structure determinations revealed a superlattice framework built up of covalently linked clusters. This superlattice is best described as two enlarged and interlaced diamond or zinc blende lattices. Because both the superlattice and the clusters display the same structural features, the crystal structure resembles the self-similarities known from fractal geometry. The optical spectrum of the cluster solution displays a sharp transition around 290 nanometers with a large Absorption coefficient (~84,000 per molar per centimeter).</abstract>
    <parentTitle language="eng">Science</parentTitle>
    <identifier type="doi">10.1126/science.267.5203.1476</identifier>
    <identifier type="issn">0036-8075</identifier>
    <identifier type="issn">1095-9203</identifier>
    <enrichment key="date_peer_review">08.03.2018</enrichment>
    <author>T. Vossmeyer</author>
    <author>Günter Reck</author>
    <author>L. Katsikas</author>
    <author>E. T. K. Haupt</author>
    <author>Burkhard Schulz</author>
    <author>H. Weller</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>superlattice</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>cluster</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>X-ray structure determination</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
  <doc>
    <id>2694</id>
    <completedYear/>
    <publishedYear>2003</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>o634</pageFirst>
    <pageLast>o635</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>59</volume>
    <type>article</type>
    <publisherName>Blackwell Publ.</publisherName>
    <publisherPlace>Oxford</publisherPlace>
    <creatingCorporation>International Union of Crystallography</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Two polymorphic forms of 2,5-bis(4-methoxycarbonylphenyl)-1,3,4-oxadiazole</title>
    <abstract language="eng">In the title compound, C13H14BN3O, the aziridine ring is an almost equilateral triangle, the CC distance being slightly shorter than the CN distances, probably because of the dative BN bond. The five-membered ring, composed of two C atoms and N, B and O atoms, is fused with the aziridine ring to form a six-membered ring with a chair conformation.</abstract>
    <parentTitle language="eng">Acta crystallographica C</parentTitle>
    <identifier type="old">2673</identifier>
    <identifier type="doi">10.1107/S0108270103022698</identifier>
    <identifier type="issn">0108-2701</identifier>
    <identifier type="issn">1600-5759</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">30.10.2003</enrichment>
    <author>Günter Reck</author>
    <author>I. Orgzall</author>
    <author>B. Schulz</author>
    <author>B. Dietzel</author>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>3110</id>
    <completedYear/>
    <publishedYear>2004</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>m134</pageFirst>
    <pageLast>m136</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>60</volume>
    <type>article</type>
    <publisherName>Blackwell Publ.</publisherName>
    <publisherPlace>Oxford</publisherPlace>
    <creatingCorporation>International Union of Crystallography</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Phenanthroline complexes of zinc and calcium carbamates</title>
    <abstract language="eng">Bis(N,N-di-n-butyl­di­thio­carbamato-?2S,S')(1,10-phenanthroline-?2N,N')­zinc(II) ethanol hemisolvate, [Zn(C9H18NS2)2(C12H8N2)]·0.5C2H6O, (I), and bis(N,N-di-n-hexyldithiocarbamato-?2S,S')­bis(1,10-phenanthroline-?2N,N')calcium(II), [Ca(C13H26NS2)2(C12H8N2)2], (II), are mixed-ligand com­plexes. In the first compound, the Zn atom has a distorted octahedral coordination, while in the second compound, the Ca atom is eight-coordinate, with four S and four N atoms forming a highly distorted cube.</abstract>
    <parentTitle language="eng">Acta crystallographica C</parentTitle>
    <identifier type="old">3183</identifier>
    <identifier type="doi">10.1107/S0108270104001441</identifier>
    <identifier type="issn">0108-2701</identifier>
    <identifier type="issn">1600-5759</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">23.02.2004</enrichment>
    <author>Günter Reck</author>
    <author>Roland Becker</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>X-ray structure analyses</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Metal-organic complexes</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Antioxidant properties</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>7043</id>
    <completedYear/>
    <publishedYear>2005</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>i35</pageFirst>
    <pageLast>i37</pageLast>
    <pageNumber/>
    <edition/>
    <issue>3</issue>
    <volume>61</volume>
    <type>article</type>
    <publisherName>Munksgaard</publisherName>
    <publisherPlace>Copenhagen</publisherPlace>
    <creatingCorporation>International Union of Crystallography</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">K6H2[TiW11CoO40].13H2O, with a monotitanoundecatungstocobaltate(II) anion</title>
    <abstract language="eng">Hexapotassium dihydrogen monotitanoundeca­tungsto­cobalt­ate(II) trideca­hydrate, K6H2[TiW11CoO40]·13H2O, crystallizes from aqueous solution in the cubic space group P 3m. The structure was refined as an inversion twin. The [TiW11CoO40]8- anion has a Keggin structure with one W-atom site occupied by titanium and a central tetra­hedral CoO4 group.</abstract>
    <parentTitle language="eng">Acta crystallographica E</parentTitle>
    <identifier type="old">7472</identifier>
    <identifier type="doi">10.1107/S1600536805005180</identifier>
    <identifier type="issn">1600-5368</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="zsBemerkung">Bis zum JCR 2011 war die Acta Crystallographica E noch enthalten. Im JCR 2012 ist die Zeitschrift nicht mehr. In Publica sollte sie vorläufig noch als JCR-Zeitschrift gelistet bleiben.  Jan Harloff-Puhr 10.7.2014</enrichment>
    <enrichment key="date_peer_review">28.02.2005</enrichment>
    <author>Werner Kraus</author>
    <author>H. Stephan</author>
    <author>A. Röllich</author>
    <author>Z. Matejka</author>
    <author>Günter Reck</author>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>7378</id>
    <completedYear/>
    <publishedYear>2005</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>352</pageFirst>
    <pageLast>355</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>T115</volume>
    <type>article</type>
    <publisherName>IoP Publ.</publisherName>
    <publisherPlace>Bristol</publisherPlace>
    <creatingCorporation>Kungliga Svenska Vetenskapsakademien</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Combining EXAFS and X-ray powder diffraction to solve structures containing heavy atoms</title>
    <abstract language="eng">Determination of structures using x-ray powder diffraction is complicated if the reflection intensities are mainly influenced by the scattering from heavy atoms and the atomic coordinates of light atoms remain uncertain. A method like EXAFS, which is sensitive to short range order, gives reliable atomic distances in the surroundings of heavy atoms with a precision of ±0.02 Å. The probability for obtaining the complete structure from x-ray powder diffraction increases if one includes parameters derived from EXAFS measurements as restraints during the procedure of structure solving. We demonstrate the potential of combining EXAFS and x-ray powder diffraction by solving the structure UO2[H2AsO4]2H2O. The procedure starts with the determination of space group and cell parameters from XRD powder data. In a second step the absolute values of the structure factor |F| are separated by iterating a decomposition formula. The heavy atom positions are determined by direct methods. In the third step atomic distances of coordination polyhedra are estimated using EXAFS. Subsequently, the complete coordination geometries around the heavy atoms including reliable distances are used as restraints in the structure solving and refinement procedure.</abstract>
    <parentTitle language="eng">Physica scripta</parentTitle>
    <identifier type="old">7823</identifier>
    <identifier type="doi">10.1238/Physica.Topical.115a00352</identifier>
    <identifier type="issn">0031-8949</identifier>
    <identifier type="issn">1402-4896</identifier>
    <identifier type="issn">0281-1847</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">09.05.2005</enrichment>
    <author>C. Hennig</author>
    <author>T. Reich</author>
    <author>Werner Kraus</author>
    <author>Günter Reck</author>
    <author>F. Prokert</author>
    <author>N. Schell</author>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>7473</id>
    <completedYear/>
    <publishedYear>2005</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume/>
    <type>poster</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Uric Acid Monohydrate a Nev Urinary Calculus Phase</title>
    <parentTitle language="eng">Tag der Chemie, Freie Universität Berlin</parentTitle>
    <identifier type="old">7924</identifier>
    <enrichment key="eventName">Tag der Chemie, Freie Universität Berlin</enrichment>
    <enrichment key="eventPlace">Berlin, Germany</enrichment>
    <enrichment key="eventStart">2005-06-08</enrichment>
    <author>Günter Reck</author>
    <collection role="fulltextaccess" number="">Weder Datei noch physisches Exemplar vorhanden ("No Access")</collection>
    <collection role="literaturgattung" number="">Präsentation</collection>
  </doc>
  <doc>
    <id>7474</id>
    <completedYear/>
    <publishedYear>2005</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume/>
    <type>poster</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">X-ray Structure Determination from Powder Diffraction Data by PowderCell</title>
    <parentTitle language="eng">Tag der Chemie, Freie Universität Berlin</parentTitle>
    <identifier type="old">7925</identifier>
    <enrichment key="eventName">Tag der Chemie, Freie Universität Berlin</enrichment>
    <enrichment key="eventPlace">Berlin, Germany</enrichment>
    <enrichment key="eventStart">2005-06-08</enrichment>
    <author>Günter Reck</author>
    <collection role="fulltextaccess" number="">Weder Datei noch physisches Exemplar vorhanden ("No Access")</collection>
    <collection role="literaturgattung" number="">Präsentation</collection>
  </doc>
  <doc>
    <id>7613</id>
    <completedYear/>
    <publishedYear>2005</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>m1373</pageFirst>
    <pageLast>m1375</pageLast>
    <pageNumber/>
    <edition/>
    <issue>7</issue>
    <volume>61</volume>
    <type>article</type>
    <publisherName>Munksgaard</publisherName>
    <publisherPlace>Copenhagen</publisherPlace>
    <creatingCorporation>International Union of Crystallography</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">[2-Carboxy-2,2',2''-nitrilotris(ethanethiolato)-kappa4N,S,S',S''](triphenyl-phosphine-kappaP)rhenium(III) acetone solvate</title>
    <abstract language="eng">The title compound, [Re(C7H12NO2S3)(C18H15P)]·C3H6O, crystallizes from a solution in chloro­formacetonecyclo­­hexane with enantiomers disordered equally over each mol­ecular site. Hydrogen bonds between the carbox­yl groups form dimers in the crystal structure.</abstract>
    <parentTitle language="eng">Acta crystallographica E</parentTitle>
    <identifier type="old">8072</identifier>
    <identifier type="doi">10.1107/S1600536805018660</identifier>
    <identifier type="issn">1600-5368</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="zsBemerkung">Bis zum JCR 2011 war die Acta Crystallographica E noch enthalten. Im JCR 2012 ist die Zeitschrift nicht mehr. In Publica sollte sie vorläufig noch als JCR-Zeitschrift gelistet bleiben.  Jan Harloff-Puhr 10.7.2014</enrichment>
    <enrichment key="date_peer_review">27.06.2005</enrichment>
    <author>E. Schiller</author>
    <author>Werner Kraus</author>
    <author>Günter Reck</author>
    <author>H. Spies</author>
    <author>H.-J. Pietzsch</author>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
</export-example>
