Thiodiacetate cobalt(II) complexes: Synthesis, structure and properties

被引:33
作者
Grirrane, A
Pastor, A
Alvarez, E
Mealli, C
Ienco, A
Masi, D
Galindo, A
机构
[1] Univ Sevilla, Univ Sevilla, Dept Quim Inorgan, Seville 41071, Spain
[2] Univ Sevilla, CSIC, Inst Invest Quim, Seville 41092, Spain
[3] CNR, ICCOM, I-50019 Florence, Italy
关键词
cobalt(II); thiodiacetate; thiodiglycolate; crystal structure;
D O I
10.1016/j.inoche.2005.02.011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The novel cobalt thiodiacetate complex [Co(tda)(H2O)](n), (1a) (tda = S(CH2COO)(2)(2-)) was synthesized from the reaction of aqueous solutions of cobalt dichloride with a 1: 1 mixture of Na2CO3 and thiodiacetic acid. A second isomer was also obtained occasionally and identified as complex [Co(tda)(H2O)(3)] (1b). The reaction of 1a with 2,2'-bipyridine (bipy) gave compound [Co(tda)(bipy)(H2O)] center dot 4H(2)O (2), which has been structurally characterized and represents, to our knowledge, the first X-ray determination of a thiodiacetate-cobalt complex. The coordination is monomeric pseudo-octahedral as determined by the typical tridentate thiodiacerate ligand with a facial configuration, the chelate bipy ligand and one water molecule. Conversely, the interaction of bis(2-pyridyl)ketone with la afforded the compound [Co{OC(OH)(2-pyridyl)(2)}(2)](+)[Htda](-) center dot 3H(2)O (3), as confirmed from an X-ray analysis. The bis(2-pyridyl) ketone ligand is hydrolyzed with a concomitant oxidation of the metal to Co(III), a process which has been previously described, while the tda ligand, displaced from the coordination sphere, is monoprotonated and acts as counterion. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:463 / 466
页数:4
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