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具有稠合二硫醇盐配体的双核铜(I)和铜(I)/银(I)配合物。

Dinuclear copper(I) and copper(I)/silver(I) complexes with condensed dithiolato ligands.

作者信息

Vicente José, González-Herrero Pablo, García-Sánchez Yolanda, Bautista Delia

机构信息

Grupo de Química Organometálica, Departamento de Química Inorgánica, Facultad de Química, Universidad de Murcia, Apdo. 4021, 30071 Murcia, Spain.

出版信息

Inorg Chem. 2008 Nov 17;47(22):10662-73. doi: 10.1021/ic8014139. Epub 2008 Oct 15.

Abstract

The Cu(III) complex Pr 4N[Cu{S 2C=( t-Bu-fy)} 2] ( 1) ( t-Bu-fy = 2,7-di- tert-butylfluoren-9-ylidene) reacts with [Cu(PR 3) 4]ClO 4 in 1:1 molar ratio in MeCN to give the dinuclear complexes [Cu 2{[SC=( t-Bu-fy)] 2S}(PR 3) n ] [ n = 2, R = Ph ( 2a); n = 3, R = To ( 3b); To = p-tolyl]. The analogue of 2a with R = To ( 2b) can be obtained from the reaction of 3b with 1/8 equiv of S 8. Compound 2b establishes a thioketene-exchange equilibrium in solution leading to the formation of [Cu 4{S 2C=( t-Bu-fy)} 2(PTo 3) 4] ( 4b) and [Cu 2{[SC=( t-Bu-fy)] 3S}(PTo 3) 2] ( 5b). Solid mixtures of 4b and 5b in varying proportions can be obtained when the precipitation of 2b is attempted using MeCN. The reactions of 1 with AgClO 4 and PPh 3, PTo 3 or PCy 3 in 1:1:4 molar ratio in MeCN afford the heterodinuclear complexes [AgCu{[SC=( t-Bu-fy)] 2S}(PR 3) 3] [R = Ph ( 6a), To ( 6b), Cy ( 6c)]. Complex 6c dissociates PCy 3 in solution to give the bis(phosphine) derivative [AgCu{[SC=( t-Bu-fy)] 2S}(PCy 3) 2] ( 7c), which undergoes the exchange of [M(PCy 3)] (+) units in CD 2Cl 2 solution to give small amounts of [Cu 2{[SC=( t-Bu-fy)] 2S}(PCy 3) 2] ( 2c) and [Ag 2{[SC=( t-Bu-fy)] 2S}(PCy 3) 2] ( 8c). Complexes 6a and b participate in a series of successive equilibria in solution, involving the dissociation of phosphine ligands and the exchange of [M(PCy 3)] (+) units to give 2a or 3b and the corresponding disilver derivatives [Ag 2{[SC=( t-Bu-fy)] 2S}(PR 3) 2] [R = Ph ( 8a), To ( 8b)], followed by thioketene-exchange reactions to give [AgCu{[SC=( t-Bu-fy)] 3S}(PR 3) 2] [R = Ph ( 9a), To ( 9b)]. Complexes 9a and b can be directly prepared from the reactions of 1 with AgClO 4 and PPh 3 or PTo 3 in 1:1:3 molar ratio in THF. The crystal structures of 3b, 6b, 6c, 7c, and 9a have been solved by single-crystal X-ray diffraction studies and, in the cases of 7c and 9a, reveal the formation of short Ag...Cu metallophilic contacts of 2.8157(4) and 2.9606(6) A, respectively.

摘要

铜(III)配合物Pr₄N[Cu{S₂C=(t-Bu-fy)}₂](1)(t-Bu-fy = 2,7-二叔丁基芴-9-亚基)在乙腈中与[Cu(PR₃)₄]ClO₄以1:1的摩尔比反应,生成双核配合物[Cu₂{[SC=(t-Bu-fy)]₂S}(PR₃)ₙ] [n = 2,R = Ph(2a);n = 3,R = To(3b);To = 对甲苯基]。R = To(2b)的2a类似物可通过3b与1/8当量的S₈反应得到。化合物2b在溶液中建立硫酮交换平衡,导致形成[Cu₄{S₂C=(t-Bu-fy)}₂(PTo₃)₄](4b)和[Cu₂{[SC=(t-Bu-fy)]₃S}(PTo₃)₂](5b)。当尝试使用乙腈沉淀2b时,可以得到不同比例的4b和5b的固体混合物。1与AgClO₄以及PPh₃、PTo₃或PCy₃在乙腈中以1:1:4的摩尔比反应,得到异双核配合物[AgCu{[SC=(t-Bu-fy)]₂S}(PR₃)₃] [R = Ph(6a),To(6b),Cy(6c)]。配合物6c在溶液中解离PCy₃,生成双(膦)衍生物[AgCu{[SC=(t-Bu-fy)]₂S}(PCy₃)₂](7c),其在CD₂Cl₂溶液中发生[M(PCy₃)]⁺单元的交换,生成少量的[Cu₂{[SC=(t-Bu-fy)]₂S}(PCy₃)₂](2c)和[Ag₂{[SC=(t-Bu-fy)]₂S}(PCy₃)₂](8c)。配合物6a和b在溶液中参与一系列连续的平衡反应,包括膦配体的解离和[M(PCy₃)]⁺单元的交换,生成2a或3b以及相应的二银衍生物[Ag₂{[SC=(t-Bu-fy)]₂S}(PR₃)₂] [R = Ph(8a),To(8b)],随后发生硫酮交换反应,生成[AgCu{[SC=(t-Bu-fy)]₃S}(PR₃)₂] [R = Ph(9a),To(9b)]。配合物9a和b可通过1与AgClO₄以及PPh₃或PTo₃在四氢呋喃中以1:1:3的摩尔比直接反应制备。通过单晶X射线衍射研究解析了3b、6b、6c、7c和9a的晶体结构,在7c和9a的情况下,分别揭示了短的Ag...Cu亲金属接触的形成,距离分别为2.8157(4) Å和2.9606(6) Å。

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