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First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands

机译:第一种杂配的二硒代次膦酸酯和硫代硒代膦酸酯镍(II)与N供体共配体的配合物

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摘要

The first heteroleptic Ni-II diselenophosphinates and thioselenophosphinates, [Ni(Se2PR2)(2)L-2] and {Ni[Se(S)PR2](2)L-2} (L = pyridine and 1-vinylimidazole), have been synthesized in high yield by the one-pot reaction of the ammonium salts NH4[Se2PR2] or NH4[Se(S)PR2] with NiBr2 (CH2Cl2/EtOH, rt, 10 min), followed by the addition of the N-heterocyclic ligands. In the solid state, all the complexes exist as mononuclear species, in which the coordination polyhedron of the Ni atom is a compressed octahedron formed by four chalcogen atoms (S and/or Se) of two bidentate chelating [R2PSe2] or [R2P(S)Se] ligands and two nitrogen atoms of two pyridine or 1-vinylimidazole molecules, arranged in trans-positions. (C) 2016 Elsevier Ltd. All rights reserved.
机译:第一杂合Ni-II二硒代次膦酸酯和硫代硒代次膦酸酯[Ni(Se2PR2)(2)L-2]和{Ni [Se(S)PR2](2)L-2}(L =吡啶和1-乙烯基咪唑)具有通过铵盐NH4 [Se2PR2]或NH4 [Se(S)PR2]与NiBr2的一锅反应(CH2Cl2 / EtOH,rt,10分钟),然后加入N-杂环,以高收率合成配体。在固态下,所有络合物均以单核形式存在,其中Ni原子的配位多面体是由两个二齿螯合物[R2PSe2]或[R2P(S)的四个硫属元素原子(S和/或Se)形成的压缩八面体。 )Se]配体和两个吡啶或1-乙烯基咪唑分子的两个氮原子,排列成转位。 (C)2016 Elsevier Ltd.保留所有权利。

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