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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/inorganics2030424</dc:identifier><dc:language>eng</dc:language><dc:creator>Caddeo, Francesco</dc:creator><dc:creator>Fernández-Moreira, Vanesa</dc:creator><dc:creator>Arca, Massimiliano</dc:creator><dc:creator>Laguna, Antonio</dc:creator><dc:creator>Lippolis, Vito</dc:creator><dc:creator>Gimeno, M.C.</dc:creator><dc:title>Gold Thione Complexes</dc:title><dc:identifier>ART-2014-98043</dc:identifier><dc:description>The reaction of the ligand Et4todit (4,5,6,7-Tetrathiocino-[1,2-b:3,4-b']-diimidazolyl-1,3,8,10-tetraethyl-2,9-dithione) with gold complexes leads to the dinuclear gold(I) complexes [{Au(C6F5)}2(Et4todit)] and [Au(Et4todit)]2(OTf)2, which do not contain any gold-gold interactions, or to the gold(III) derivative [{Au(C6F5)3}2(Et4todit)]. The cristal structures have been established by X-ray diffraction studies and show that the gold centers coordinate to the sulfur atoms of the imidazoline-2-thione groups.</dc:description><dc:date>2014</dc:date><dc:source>http://zaguan.unizar.es/record/60655</dc:source><dc:doi>10.3390/inorganics2030424</dc:doi><dc:identifier>http://zaguan.unizar.es/record/60655</dc:identifier><dc:identifier>oai:zaguan.unizar.es:60655</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2013-48635-C2-1-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FSE/E77</dc:relation><dc:identifier.citation>Inorganics 2, 3 (2014), 424-432</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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