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首页> 外文期刊>Journal of Organometallic Chemistry >The Staudinger reaction of platinum(II)- and palladium(II)-coordinated 2-(azidomethyl)phenyl isocyanide. X-ray structure of trans-[PtCl{CN(H)C6H4-2-CH2N(H)} (PPh3)(2)][BF4] center dot CDCl3 center dot H2O
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The Staudinger reaction of platinum(II)- and palladium(II)-coordinated 2-(azidomethyl)phenyl isocyanide. X-ray structure of trans-[PtCl{CN(H)C6H4-2-CH2N(H)} (PPh3)(2)][BF4] center dot CDCl3 center dot H2O

机译:铂(II)-和钯(II)配位的2-(叠氮基甲基)苯基异氰酸酯的斯托丁格反应。反式-[PtCl {CN(H)C6H4-2-CH2N(H)}(PPh3)(2)] [BF4]中心点CDCl3中心点H2O的X射线结构

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摘要

2-(Azidomethyl)phenyl isocyanide, 2-(CH2N3)C(6)H(4)NdropC (AziNC), coordinates to some cationic Pt(II) and Pd(II) species to afford isocyanide complexes of the type trans-[MCl(AziNC(PPh3)(2)][BF4] (M = Pt, 1; Pd, 2). AziNC is coordinated also in some neutral Pt(II) and Pd(II) species such as [MCl2(AziNC)(2)] (M = Pt, 3; Pd, 4) derived from the reactions of 2 equiv. of AziNC with [PtCl2(COD)] and [PdCl2(MeCN)(2)], respectively. Complexes 1 and 2 react with 1 equiv. of PPh3 affording the heterocyclic carbene complexes trans-[MCl{CN(H)C6H4-2-CH2N(H)}(PPh3)(2)][BF4] (M = Pt, 5; Pd, 6). Complexes 3 and 4 react with 1 equiv. of PPh3 displacing the isocyanide with the formation of the complexes cis-[MCl2(AziNC(PPh3)](M = Pt, 7; Pd, 8). These latter ones react with 2 equiv. of PPh3 affording as the final products the cationic carbene species trans-[MCl{CN(H)C6H4-2-CH2N(H)}(PPh3)(2)][Cl] (M = Pt, 9; Pd, 10). Complex 5 was also characterized by single crystal X-ray diffraction. The carbene complex is square-planar and the angle formed between the platinum square plane and the heterocyclic carbene ligand is 87.9(2)degrees. The C(1)-N(1) and C(1)-N(2) bond distances in the latter of 1.32(2) and 1.30(2) Angstrom, respectively, are short for a single bond and indicate extensive pi-bonding between the nitrogen atoms and the carbene carbon. (C) 2003 Elsevier B.V. All rights reserved. [References: 54]
机译:2-(叠氮基甲基)苯基异氰酸酯,2-(CH2N3)C(6)H(4)NdropC(AziNC)与某些阳离子Pt(II)和Pd(II)配位,以提供反式-[ MCl(AziNC(PPh3)(2)] [BF4](M = Pt,1; Pd,2)。AziNC在某些中性Pt(II)和Pd(II)物种(例如[MCl2(AziNC)( 2)](M = Pt,3; Pd,4)分别来自2当量AziNC与[PtCl2(COD)]和[PdCl2(MeCN)(2)]的反应,配合物1和2与1当量的PPh3,得到杂环卡宾配合物,反式-[MCl {CN(H)C6H4-2-CH2N(H)}(PPh3)(2)] [BF4](M = Pt,5; Pd,6)。配合物3和4与1当量的PPh3反应,置换异氰酸酯,形成配合物cis- [MCl2(AziNC(PPh3)](M = Pt,7; Pd,8),而后者则与2当量反应。 PPh3的最终产物为阳离子卡宾物种,反式-[MCl {CN(H)C6H4-2-CH2N(H)}(PPh3)(2)] [Cl](M = Pt,9; Pd,10)配合物5还通过单晶X射线衍射表征。 ex是正方形平面,铂正方形平面与杂环卡宾配体之间形成的夹角为87.9(2)度。后者中的C(1)-N(1)和C(1)-N(2)键距分别为1.32(2)和1.30(2)埃,对于单键而言较短,表明存在广泛的pi-氮原子和卡宾碳之间的键合。 (C)2003 Elsevier B.V.保留所有权利。 [参考:54]

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