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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/c7cc03713a</dc:identifier><dc:language>eng</dc:language><dc:creator>Cámara, J.</dc:creator><dc:creator>Blanco, M.C.</dc:creator><dc:creator>Laguna, A.</dc:creator><dc:creator>Naumov, P.</dc:creator><dc:creator>Gimeno, M.C.</dc:creator><dc:title>A stable gold(i)-enyne species obtained by alkyne carboauration in a complex rearrangement</dc:title><dc:identifier>ART-2017-104765</dc:identifier><dc:description>An unprecedented tetranuclear gold derivative with unusual gold-enyne moieties is prepared by a mild and neat rearrangement of a dinuclear gold complex with a bridging bis(diphenylphosphino)alkyne and terminal alkynyl ligands. The complex originates as a consequence of an intramolecular addition of the AuCCTol fragment to the internal diphosphine triple bond Ph2PCCPPh2. The crystal structure of the tetranuclear complex shows a dinuclear metallacycle with a very short Au¿Au bond interaction and bridging phosphino-enyne ligands. This disposition clearly stabilises the elusive vinyl gold species omnipresent as intermediates in gold-catalysed reactions.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/169333</dc:source><dc:doi>10.1039/c7cc03713a</dc:doi><dc:identifier>http://zaguan.unizar.es/record/169333</dc:identifier><dc:identifier>oai:zaguan.unizar.es:169333</dc:identifier><dc:identifier.citation>Chemical Communications 53, 66 (2017), 9202-9205</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights></dc:dc>

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