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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:10.1002/chem.201705509</dc:identifier><dc:language>eng</dc:language><dc:creator>Baya, M.</dc:creator><dc:creator>Pérez-Bitrián, A.</dc:creator><dc:creator>Martínez-Salvador, S.</dc:creator><dc:creator>Martín, A.</dc:creator><dc:creator>Casas, J.M.</dc:creator><dc:creator>Menjón, B.</dc:creator><dc:creator>Orduna, J.</dc:creator><dc:title>Gold(II) Trihalide Complexes from Organogold(III) Precursors</dc:title><dc:identifier>ART-2018-104591</dc:identifier><dc:description>The mononuclear gold(II) halide complexes [AuCl3]- and [AuBr3]- are formed in the gas phase by collision-induced homolytic splitting of the only Au-C bond in the monoalkylgold(III) precursors [CF3AuX3]-. The geometries of the whole series of [AuX3]- complexes (X=F, Cl, Br, I) have been calculated by DFT methods. It has also been found that the neutral AuX2 molecules behave as unsaturated species, showing significant affinity for an additional X- ligand. Moreover, in the open-shell [AuX3]- anions, homolytic splitting of one of the Au-X bonds and formation of the lower-valent [AuX2]- anions is favored over non-reducing halide dissociation. They should therefore be prone to disproportionation.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/78288</dc:source><dc:doi>10.1002/chem.201705509</dc:doi><dc:identifier>http://zaguan.unizar.es/record/78288</dc:identifier><dc:identifier>oai:zaguan.unizar.es:78288</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E21</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MEC/FPU15-03940</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2015-67461-P</dc:relation><dc:identifier.citation>Chemistry - A European Journal 24, 7 (2018), 1514-1517</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/openAccess</dc:rights></dc:dc>

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