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二核金(I)二硫代膦酸酯配合物的合成与结构以及二硫代膦酸酯配合物与膦的反应:多样的配位类型

Syntheses and structures of dinuclear gold(I) dithiophosphonate complexes and the reaction of the dithiophosphonate complexes with phosphines: diverse coordination types.

作者信息

Maspero Angelo, Kani Ibrahim, Mohamed Ahmed A, Omary Mohammad A, Staples Richard J, Fackler John P

机构信息

Department of Chemistry and Laboratory for Molecular Structure and Bonding, Texas A&M University, P.O. Box 30012 College Station, Texas 77842-3012, USA.

出版信息

Inorg Chem. 2003 Aug 25;42(17):5311-9. doi: 10.1021/ic034114y.

Abstract

The dinuclear gold(I) dithiophosphonate complex, [Au(2)(dtp)(2)] (1), where dtp = S(2)P(R)(OR') with R = p-C(6)H(4)OCH(3); R'= c-C(5)H(9), has been synthesized and its reaction studied with the phosphine ligands PPh(3) and Ph(2)P(CH(2))(n)PPh(2) (n = 1-4). Compound 1 contains two gold atoms homobridged by the anionic dithiophosphonate ligand, forming an eight-membered ring complex in a chair form. After the reaction of 1 with diphosphine ligands, the dinuclear open-ring complexes Au(2)(dppm)(dtp)(2) (2), Au(2)(dppe)(dtp)(2) (3), Au(2)(dppp)(dtp)(2) (4), Au(2)(dppb)(dtp)(2) (5) were formed (dppm = diphenylphosphinomethane; dppe = diphenylphosphinoethane; dppp = diphenylphosphinopropane; dppb = diphenylphosphinobutane). The reaction with dppm is stoichiometry-dependent. Thus, when 1 reacts with 2 equiv of dppm, the ionic complex [Au(2)(dppm)(2)(dtp)]dtp forms. This dtp counterion was exchanged with tetrafluoroborate to yield [Au(2)(dppm)(2)(dtp)]BF(4), the crystallization of which afforded two interconvertible isomers, 6-yellow and 7-white. Reaction of 1 with PPh(3) affords the tetracoordinate mononuclear complex [Au(dtp)(PPh(3))(2)] (8). The molecular structures of 1-8 were confirmed by X-ray crystallography and show multiple coordination modes and geometries. The crystal structures of 1 and its reaction products with dppm (2, 6, 7) show short intramolecular Au.Au aurophilic bonding interactions of 2.95-3.10 A while no intermolecular interactions were discernible. However, reaction products of 1 with longer-chain Ph(2)P(CH(2))(n)PPh(2) ligands, n = 2-4, exhibit structures that lack both intra- and intermolecular Au.Au interactions.

摘要

二核金(I)二硫代膦酸酯配合物[Au₂(dtp)₂](1),其中dtp = [S₂P(R)(OR')]⁻,R = p-C₆H₄OCH₃;R' = c-C₅H₉,已被合成,并研究了其与膦配体PPh₃和Ph₂P(CH₂)ₙPPh₂(n = 1 - 4)的反应。化合物1包含两个由阴离子二硫代膦酸酯配体同桥连的金原子,形成一个椅式八元环配合物。1与二膦配体反应后,形成了二核开环配合物Au₂(dppm)(dtp)₂(2)、Au₂(dppe)(dtp)₂(3)、Au₂(dppp)(dtp)₂(4)、Au₂(dppb)(dtp)₂(5)(dppm = 二苯基膦基甲烷;dppe = 二苯基膦基乙烷;dppp = 二苯基膦基丙烷;dppb = 二苯基膦基丁烷)。与dppm的反应取决于化学计量比。因此,当1与2当量的dppm反应时,形成离子配合物[Au₂(dppm)₂(dtp)]dtp。该dtp抗衡离子与四氟硼酸根交换,得到[Au₂(dppm)₂(dtp)]BF₄,其结晶得到两种可相互转化的异构体,6 - 黄色和7 -白色。1与PPh₃反应得到四配位单核配合物[Au(dtp)(PPh₃)₂](8)。通过X射线晶体学确定了1 - 8的分子结构,它们显示出多种配位模式和几何构型。1及其与dppm的反应产物(2、6、7)的晶体结构显示出2.95 - 3.10 Å的短分子内金 - 金亲金相互作用,而没有可识别的分子间相互作用。然而,1与长链Ph₂P(CH₂)ₙPPh₂配体(n = 2 - 4)的反应产物显示出既缺乏分子内金 - 金相互作用也缺乏分子间金 - 金相互作用的结构。

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