Nickel(II) complexes with N-(thio)phosphorylthioureas AdNHC(S)NHP(X)(OiPr)2:: Versatile coordination of phosphoryl (X = O) and thiophosphoryl (X = S) derivatives

被引:29
|
作者
Safin, Damir A. [1 ,3 ]
Sokolov, Felix D. [1 ]
Szyrwiel, Lukasz [2 ]
Babashkina, Maria G. [1 ]
Gimadiev, Timur R. [1 ]
Hahn, F. Ekkehardt [3 ]
Kozlowski, Henryk [2 ]
Krivolapov, Dmitriy B. [4 ]
Litvinov, Igor A. [4 ]
机构
[1] Kazan VI Lenin State Univ, AM Butlerov Chem Inst, Kazan 420008, Russia
[2] Univ Wroclaw, Fac Chem, PL-50383 Wroclaw, Poland
[3] Univ Munster, Inst Anorgan & Analyt Chem, D-48149 Munster, Germany
[4] AE Arbuzov Inst Organ & Phys Chem, Kazan 420088, Russia
关键词
chelate; hydrogen bond; nickel complexes; crystal structures; N-(thio)phosphorylthiourea;
D O I
10.1016/j.poly.2008.04.014
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of the potassium salts of N-(thio)phosphorylated thioureas of the common formula AdN(H)C(S)N(H)P(X)(OiPr)(2) (X=O, HLI; X=S, HLII) with the Ni(II) cation in aqueous EtOH leads to [Ni(L-I,L-II)(2)] chelate complexes. The molecular structures of the thioureas HLI,II and the complexes [Ni(L'N,S)2] and [Ni(L-II-S,S')(2)] were elucidated by single crystal X-ray diffraction analysis, IR, H-1 and P-31 NMR spectroscopy and microanalysis. In the complex [Ni(L-I)(2)], the metal center is found to be in a square-planar N2S2 environment formed by the C=S sulfur atoms and the P-N nitrogen atoms of two deprotonated L-I ligands. The ligands are in a trans configuration. The Ni(II) atom in complex [Ni(L-II)(2)], with the deprotonated thiourea L-II, is coordinated in a square-planar fashion by the C=S and P=S sulfur atoms of two anionic ligands. The ligands are in a cis configuration. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2271 / 2276
页数:6
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