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首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Toward model complexes of Co-containing nitrile hydratases: synthesis, complete characterization and reactivity toward ligands such as CN- and NO of the first square planar Co-III complex with two different carboxamido nitrogens and two thiolato sulf
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Toward model complexes of Co-containing nitrile hydratases: synthesis, complete characterization and reactivity toward ligands such as CN- and NO of the first square planar Co-III complex with two different carboxamido nitrogens and two thiolato sulf

机译:含钴腈水合酶的模型络合物:具有两个不同的羧酰胺氮和两个硫醇基硫的第一方平面Co-III络合物的配体(如CN-和NO)的合成,完全表征和反应性

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A [Co-III(N2S2)]NEt4 complex, with two carboxamido nitrogens and two alkylthiolato sulfurs, was prepared from N,N'-(2-thioacetyl-isobutyryl)-2-aminobenzylamine, and characterized. It crystallizes with a distorted square planar structure including two short Co-N bonds (approximate to 1.882 Angstrom) and two short Co-S bonds (approximate to 2.134 Angstrom). The ligand defines an Ii-atom chelate, which may be Co ligands in the mean plane of Go-containing nitrile hydratase. The Co-III oxidation state, reversibly reduced at -1.13 V(vs. SCE) and irreversibly oxidized at +1.29 V (vs. SCE) in DMF, is stable over a 2 V potential range. From the temperature dependence of its magnetic susceptibility, cobalt(III) was found to be in an S = 1 triplet ground state, in agreement with the broad resonances observed in its H-1-NMR spectrum. Preliminary spectral studies showed that this complex does not interact with imidazole, H2O or HO-, but binds two CN- anions or two NO molecules. The IR spectrum of the dinitrosyl complex exhibits two NO stretches at 1765 and 1820 cm(-1), in the range previously observed for dinitrosylated complexes derived from cobalt(I). This result suggests that, similarly to Fe NHases, Co NHases might readily bind NO. (C) 2000 Elsevier Science S.A. All rights reserved. [References: 26]
机译:由N,N′-(2-硫代乙酰基-异丁酰基)-2-氨基苄胺制备具有两个羧酰胺基氮和两个烷基硫代巯基硫的[Co-III(N2S2)] NEt4配合物,并对其进行表征。它以扭曲的正方形平面结构结晶,该结构包括两个短的Co-N键(约1.882埃)和两个短的Co-S键(约2.134埃)。所述配体定义了II原子的螯合物,其可以是含Go的腈水合酶的平均平面上的Co配体。在DMF中,Co-III的氧化态在-1.13 V(vs。SCE)下可逆还原,而在+1.29 V(vs. SCE)下不可逆地氧化,在2 V电位范围内是稳定的。根据其磁化率的温度依赖性,发现钴(III)处于S = 1三重态基态,与其在H-1-NMR光谱中观察到的宽共振相符。初步的光谱研究表明,该配合物不与咪唑,H2O或HO-相互作用,但结合两个CN-阴离子或两个NO分子。二亚硝酰基配合物的红外光谱在1765和1820 cm(-1)处显示两个NO延伸,在先前观察到的源自钴(I)的二亚硝基化配合物的范围内。该结果表明,与Fe NHases相似,Co NHases可能容易结合NO。 (C)2000 Elsevier Science S.A.保留所有权利。 [参考:26]

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