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首页> 外文期刊>International Journal of Quantum Chemistry >Syntheses and solid-state structures of molecular and extended silver(I) complexes of 4-isocyano-3,5-diisopropylbenzonitrile
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Syntheses and solid-state structures of molecular and extended silver(I) complexes of 4-isocyano-3,5-diisopropylbenzonitrile

机译:4-异氰基-3,5-二异丙基苄腈的分子和扩展银(I)配合物的合成和固态结构

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摘要

The molecular complexes [Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)]X, 1 (a, X = BF4; b, X = SO3CF3), have been prepared by reaction of the respective silver(I) salts with 2 equivalents of the isocyanide in benzene solution. Reaction of 1b with an equivalent amount of AgSO3CF3 in benzene solution gave the extended molecular solid {[Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)]SO3CF3}(n), 2. The solid-state structures of la and 2 have been determined by single-crystal X-ray crystallography. Compound 1a crystallizes in the triclinic space group P (1) over bar with a = 10.506(2) Angstrom, b = 12.838(2) Angstrom, c = 12.974(2) Angstrom, alpha = 100.65(2)degrees, beta = 101.52(2)degrees, gamma = 105.37(2)degrees, V = 1600.1(7) Angstrom(3), and Z = 2 with R = 0.056 and wR = 0.087. Compound 2 crystallizes in the triclinic space group P (1) over bar with a = 9.6868(8) Angstrom, b = 10.551(1) Angstrom, c = 11.559(1) Angstrom, alpha = 76.350(9)degrees, beta = 82.037(9)degrees, gamma = 71.481(9)degrees, V = 1086.0(4) Angstrom(3), and Z = 1 with R = 0.027 and wR = 0.036. Compound 1a may be described as a dicoordinate silver(I) complex with a significantly bent linear coordination geometry (C-Ag-C 156.1(2)degrees). The bending of the diisocyanide metal group is caused by the interaction with the BF4 anion (shortest Ag-F distance 2.534(8) Angstrom). The nitrile groups in 1b are not engaged in any directional intermolecular interaction. The solid-state structure of 2 consists of linear chains of [Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)]SO3CF3 units, whereby each silver ion is coordinated to one isocyano group and one nitrile group of consecutive cyanoisocyanoarene ligands, These linear chains are arranged in antiparallel fashion to form infinite sheets. Within the sheets, the silver ions of pairs of chains are pulled near each other by electrostatic interactions with the SO3CF3 anions, These double chains are held together primarily by pi interactions of the cyanoisocyanoarene groups. (C) 2000 Academic Press. [References: 35]
机译:分子配合物[Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)] X,1(a,X = BF4; b,X = SO3CF3)已制备各自的银(I)盐与2当量的异氰化物在苯溶液中。 1b与等量的AgSO3CF3在苯溶液中的反应得到扩展的分子固体{[Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)] SO3CF3}(n),2。 1a和2的固态结构已经通过单晶X射线晶体学确定。化合物1a在三边形空间群P(1)中结晶成a = 10.506(2)埃,b = 12.838(2)埃,c = 12.974(2)埃,alpha = 100.65(2)度,beta = 101.52 (2)度,伽玛= 105.37(2)度,V = 1600.1(7)埃(3),Z = 2,R = 0.056,wR = 0.087。化合物2在棒上的三斜晶空间群P(1)中结晶,其a = 9.6868(8)埃,b = 10.551(1)埃,c = 11.559(1)埃,alpha = 76.350(9)度,beta = 82.037 (9)度,γ= 71.481(9)度,V = 1086.0(4)埃(3),Z = 1,R = 0.027,wR = 0.036。化合物1a可描述为具有显着弯曲的线性配位几何形状(C-Ag-C 156.1(2)度)的双配位银(I)配合物。二异氰化物金属基团的弯曲是由与BF4阴离子的相互作用引起的(最短的Ag-F距离为2.534(8)埃)。 1b中的腈基不参与任何方向的分子间相互作用。 2的固态结构由[Ag(4-CN-3,5-i-Pr-2-C6H2CN)(2)] SO3CF3单元的线性链组成,其中每个银离子与一个异氰基和一个配位连续的氰基异氰基亚芳基配体的腈基,这些线性链以反平行方式排列以形成无限片。在片材中,成对链的银离子通过与SO3CF3阴离子的静电相互作用而彼此靠近。这些双链主要通过氰基异氰基亚芳基的pi相互作用保持在一起。 (C)2000年学术出版社。 [参考:35]

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