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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and characterization of two tris-chelate complexes of cobalt(III) with 3,5-dimethyl-1-(N-methyl/ethyl) thiocarbamyl-pyrazole (HL1, HL2) - biologically important bidentate ligands with one ambidentate donor site
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Synthesis and characterization of two tris-chelate complexes of cobalt(III) with 3,5-dimethyl-1-(N-methyl/ethyl) thiocarbamyl-pyrazole (HL1, HL2) - biologically important bidentate ligands with one ambidentate donor site

机译:钴(III)与3,5-二甲基-1-(N-甲基/乙基)硫代氨基甲酰基吡唑(HL1,HL2)的两种三螯合物的合成和表征-生物上重要的双齿配体,带有一个歧义的供体位点

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摘要

Cobalt(III) complexes, of two potentially pyrazole-derived bidentate ligands (with one ambidentate donor site), 3,5-dimethyl-1-(N-methyl/ethyl)thiocarbamylpyrazole (HL1 for N-methyl, HL2 for N-ethyl) have been synthesized and characterized by elemental analyses. IR, UV-Vis and H-1 NMR spectral studies. The structure of Co(L-2)(3) has been determined by single-crystal X-ray diffraction studies. The complex (triclinic, space group P (1) over bar) has a distorted octahedral structure with the ambidentate ligands coordinated to the Co(III) ion as uninegative bidentate chelating agents via the pyrazole ring nitrogen (tertiary) and the thiocarbamyl iminyl nitrogen atoms. The distortion from the regular octahedral geometry is ascribed to the stereochemical limitations imposed by the planar bidentate ligands. (C) 2000 Elsevier Science B.V. All rights reserved. [References: 14]
机译:两个潜在的吡唑衍生的双齿配体(具有一个不明确的供体位点),3,5-二甲基-1-(N-甲基/乙基)硫代氨基甲酰基吡唑的钴(III)配合物(对于N-甲基为HL1,对于N-乙基为HL2 )已通过元素分析合成并表征。 IR,UV-Vis和H-1 NMR光谱研究。 Co(L-2)(3)的结构已通过单晶X射线衍射研究确定。配合物(三斜晶系,P上的空间群P(1),具有扭曲的八面体结构)的双配体配位体通过吡唑环氮(叔)和硫代氨基甲酰基亚氨基氮原子与Co(III)离子配位为Co(III)双齿螯合剂。规则八面体几何形状的变形归因于平面二齿配体施加的立体化学限制。 (C)2000 Elsevier Science B.V.保留所有权利。 [参考:14]

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