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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:language>eng</dc:language><dc:creator>Blanco, M. C</dc:creator><dc:creator>Fernandez, E. J</dc:creator><dc:creator>Lopez De Luzuriaga, J. M</dc:creator><dc:creator>Olmos, M. E</dc:creator><dc:creator>Crespo, O.</dc:creator><dc:creator>Gimeno, M. C</dc:creator><dc:creator>Laguna, A.</dc:creator><dc:creator>Jones, P. G</dc:creator><dc:title>Heteropolynuclear phosphide complexes: phosphorus as unique atom bridging coinage metal centres.</dc:title><dc:identifier>ART-2000-50168</dc:identifier><dc:description>In this paper we describe the synthesis and reactivity of the diphenylphosphine derivatives [Au(C6F5)(PPh2H)] and trans-[Au(C6F5)2(PPh2H)2]ClO4. Reactions of the latter or the neutral [Au(C6F5)3(PPh2H)] with the appropriate Group 11 metal reagents (M=Au, Ag, Cu) in the presence of acetylacetonate afford a series of novel AuIII-M phosphido-bridged complexes, which have been scarcely represented to date. The crystal structure of the tetranuclear [{Au(C6F5)2(μ-PPh2)2Ag}2] and the dinuclear [Au(C6F5)3(μ-PPh2)M(PPh3)] (M=Au, Ag) complexes were established by X-ray diffraction methods. The synthesis and deprotonating activity of the anionic gold(III) complex PPN[Au(C6F5)3(acac)] (PNN=[N(PPh3)2]+) was studied.</dc:description><dc:date>2000</dc:date><dc:source>http://zaguan.unizar.es/record/168602</dc:source><dc:identifier>http://zaguan.unizar.es/record/168602</dc:identifier><dc:identifier>oai:zaguan.unizar.es:168602</dc:identifier><dc:identifier.citation>Chemistry - A European Journal 6, 22 (2000), 4116-23</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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