Synthesis, characterisation and X-ray structures of diorganotin(IV) and iron(III) complexes of dianionic terdentate Schiff base ligands

被引:65
作者
Labisbal, E [1 ]
Rodríguez, L [1 ]
Sousa-Pedrares, A [1 ]
Alonso, M [1 ]
Vizoso, A [1 ]
Romero, J [1 ]
García-Vázquez, JA [1 ]
Sousa, A [1 ]
机构
[1] Univ Santiago de Compostela, Dept Quim Inorgan, Santiago De Compostela 15782, Spain
关键词
organotin(IV) complexes; iron(III) complexes; Schiff base ligands; amide ligand; crystal structure; Sn-119; NMR;
D O I
10.1016/j.jorganchem.2005.09.052
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Diorganotin(IV) complexes, [SnR2L] (1)-(4), (R = Me, Ph), of the terdentate Schiff bases N-[(2-pyrroyl)methylideiie]-N'-tosylbenzene-1,2-diamine (H2L1) and N-[(2-hydroxyphenyl)metylidetie]-N'-tosylbenzene-1,2-diamine (H2L2) have been synthesised. The complexes were obtained by addition of the appropriate ligand to a methanol suspension of the corresponding diorganotin(IV) dichloride in the presence of triethylamine. However, the reaction between the precursor [eta(5)-C5H5Fe(CO)(2)](2)SnCl2 and the Schiff bases in the presence of triethylamine gave [Et3NH][FeL21] (5) and [Et3NH][FeL22] (6), respectively. The crystal structures of the ligands and complexes have been studied by X-ray diffraction. The structure of [SnR2L] complexes shows the tin to be five-coordinate in a distorted square pyramidal environment with the dianionic ligand acting in a terdentate manner. In 5 and 6, the iron atorn is in a slightly distorted octahedral environment and is meridionally coordinated by two ligands. Spectroscopic data for the ligands and complexes (IR, H-1, C-13 and Sn-119 NMR and mass spectra) are discussed and related to the structural information. (c) 2005 Elsevier B.V. All rights reserved.
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页码:1321 / 1332
页数:12
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