Reactivity of organogold compounds with B(C6F5)3: gold-boron transmetalation via [sigma]-B/[pi]-Au species

The reactions of gold-acetylides with B(C6F5)3 afford alkynyl borate species and cationic π-coordinated gold complexes. The analogous reactions with aryl gold species generate gem-diaurated compounds containing a borate counteranion. These new σ-B/π-Au alkynyl borate complexes can be employed as act...

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Hauptverfasser: Hansmann, Max M. (VerfasserIn) , Rominger, Frank (VerfasserIn) , Boone, Michael P. (VerfasserIn) , Stephan, Douglas W. (VerfasserIn) , Hashmi, A. Stephen K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 26, 2014
In: Organometallics
Year: 2014, Jahrgang: 33, Heft: 17, Pages: 4461-4470
ISSN:1520-6041
DOI:10.1021/om5006885
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/om5006885
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Verfasserangaben:Max M. Hansmann, Frank Rominger, Michael P. Boone, Douglas W. Stephan, and A. Stephen K. Hashmi

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520 |a The reactions of gold-acetylides with B(C6F5)3 afford alkynyl borate species and cationic π-coordinated gold complexes. The analogous reactions with aryl gold species generate gem-diaurated compounds containing a borate counteranion. These new σ-B/π-Au alkynyl borate complexes can be employed as active catalysts in homogeneous catalysis and represent a new silver-free activation pathway. The new alkynyl borate species are fully characterized, and the alkyne fragments are shown to be bound in a σ-B/π-Au fashion. Upon prolonged heating, these compounds undergo a slow C6F5 group transfer to gold affording LAuC6F5 species. 
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