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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:10.1039/c5sc01578b</dc:identifier><dc:language>eng</dc:language><dc:creator>Martínez-Salvador, S.</dc:creator><dc:creator>Falvello, L.R.</dc:creator><dc:creator>Martín, A.</dc:creator><dc:creator>Menjón, B.</dc:creator><dc:title>A hexanuclear gold carbonyl cluster</dc:title><dc:identifier>ART-2015-92037</dc:identifier><dc:description>The hexanuclear gold carbonyl cluster [PPh4]2[Au6(CF3)6Br2(CO)2] (4) has been obtained by spontaneous self-assembly of the following independent units: CF3AuCO (1) and [PPh4][Br(AuCF3)2] (3). The cyclo-Au6 aggregate 4, in which the components are held together by unassisted, fairly strong aurophilic interactions (Au¿Au ~310 pm), exhibits a cyclohexane-like arrangement with chair conformation. These aurophilic interactions also result in significant ¿(CO) lowering: from 2194 cm-1 in the separate component 1 to 2171 cm-1 in the mixed aggregate 4. Procedures to prepare the single-bridged dinuclear component 3 as well as the mononuclear derivative [PPh4][CF3AuBr] (2) are also reported.</dc:description><dc:date>2015</dc:date><dc:source>http://zaguan.unizar.es/record/58366</dc:source><dc:doi>10.1039/c5sc01578b</dc:doi><dc:identifier>http://zaguan.unizar.es/record/58366</dc:identifier><dc:identifier>oai:zaguan.unizar.es:58366</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E21</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2012-35251</dc:relation><dc:identifier.citation>Chemical Science 6, 10 (2015), 5506-5510</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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