Copper(I) bromide complexes from 1,2-bis(diphenylphosphano) benzene and some heterocyclic thiones

被引:40
作者
Kaltzoglou, A
Cox, PJ
Aslanidis, P [1 ]
机构
[1] Robert Gordon Univ, Sch Pharm, Aberdeen AB10 1FR, Scotland
[2] Aristotle Univ Thessaloniki, Fac Chem, Inorgan Chem Lab, GR-54124 Thessaloniki, Greece
关键词
copper; sulfur heterocycles; 1,2-bis(diphenylphosphano)benzene complexes; crystal structures; luminescence;
D O I
10.1016/j.ica.2005.04.042
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis, characterization and solid state emission properties of a series of mixed-ligand copper(I)bromide complexes containing 1,2-bis(diphenylphosphano)benzene (dppbz) and some heterocyclic thiones (L) are reported. The complexes are readily synthesized by the addition of the appropriate thione to a CuBr-diphosphane adduct in acetonitrile/methanol or acetone solution. The molecular structures of [CuBr(dppbz)(py2SH)], [CuBr(dppbz)(pymtH)] and [CuBr(dppbz)(imdtH(2))] were established by single-crystal X-ray diffraction. Each of these structures features a tetrahedral copper(l) centre with two phosphorus atoms from the chelating diphos ligand, one bromine and the exocyclic sulfur atom of the heterocyclic thioamide unit. Slow decomposition of the mixed-ligand complexes via ligand dissociation occurs when their chloroform solutions are left to stand at room temperature for several weeks. On the basis of elemental analysis, NMR and IR spectra, the resulting coloured crystals are found to contain phosphane-free coordination polymers of composition [CuBr(L)]. At room temperature, some of the molecular complexes in the solid state exhibit strong emission assigned to a metal-ligand charge transfer of type Cu(I) -> pi*(PPh2). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:3048 / 3056
页数:9
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