Reactivity of an acetylenephosphino gold(III) precursor:: Addition to the triple bond or formation of alkynyl derivatives

被引:31
作者
Bardají, M
Laguna, A [1 ]
Jones, PG
机构
[1] Univ Zaragoza, Dept Quim Inorgan, Inst Ciencia Mat Aragon, CSIC, E-50009 Zaragoza, Spain
[2] Tech Univ Braunschweig, Inst Anorgan & Analyt Chem, D-38023 Braunschweig, Germany
关键词
D O I
10.1021/om010385+
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We have synthesized the gold(III) complex Au(C6F5)(3)(PPh2CCH) (1), containing an acetylene moiety. Reactions with sodium alkoxides lead chemoselectively and regioselectively to gold(III) complexes containing the new ligand (2-alkoxyethenyl)diphenylphosphine or (2,2-dialkoxyethyl)diphenylphosphine, via a single or double alcohol addition to the acetylenephosphine fragment. Reaction of complex I with gold(I) or silver(I) acetylacetonato derivatives affords di-, tri-, or tetranuclear alkynyl-phosphino complexes, namely Au-III(C6F5)(3)(PPh2CC)-M-I(PPh3) (M = Au, Ag), {Au-III(C6F5)(3)(PPh2CC)}(2)Au-I, and {Au-III(C6F5)(3)(PPh2CC)Au-I}(2)(mu -PPh2CH2CH2PPh2). The crystal structures of Au(C6F5)(3)(PPh2CH2CH(OMe)(2)) and Au-III(C6F5)(3)(PPh2CC)Au-I(PPh3) have been determined by X-ray diffraction studies. Luminescence studies in the solid state show that only the tetranuclear derivative is luminescent at room temperature.
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页码:3906 / 3912
页数:7
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