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Synthesis and characterization of copper(I) complexes from triphenylphosphine and isatin Schiff bases of semi- and thiosemicarbazide

机译:由三苯基膦和半缩氨基脲和二巯基氨基脲的靛蓝席夫碱合成和表征铜(I)配合物

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摘要

The reaction of isatin-3-thiosemicarbazone (ITC, 1) or isatin-3-semicarbazone (ISC, 2) with nitrato bis(triphenylphosphine)copper(I) gave the four coordinate copper(I) complexes [Cu(PPh3)2(ITC)]NO3 (3) and [Cu(PPh3)2(ISC)]NO3 (4). The synthesized complexes were characterized by FT-IR, UV-VIS, Raman and elemental analysis. The crystal structure of 3 was investigated by single crystal X-ray diffraction. The ITC coordinates to the copper(I) ion in a bidentate fashion via the N(imine) and S atoms which along with two triphenylphosphine ligands form a tetracoordinate complex. The complex has a distorted tetrahedral coordination environment. Crystal data at 150.0 K: space group P21/c with a = 12.5777(4). b= 15.2062(5), c = 21.9057(7) A, β = 95.628(3)~0, Z = 4, R1 =0.049.
机译:Isatin-3-thiosemicarbazone(ITC,1)或isatin-3-semicarbazone(ISC,2)与硝酸双(三苯基膦)铜(I)的反应生成了四个配位的铜(I)络合物[Cu(PPh3)2( (ITC)] NO3(3)和[Cu(PPh3)2(ISC)] NO3(4)。通过FT-IR,UV-VIS,拉曼和元素分析对合成的配合物进行表征。通过单晶X射线衍射研究3的晶体结构。 ITC通过N(亚胺)和S原子与二价铜离子配位,它们与两个三苯基膦配体一起形成四配位络合物。该复合物具有扭曲的四面体配位环境。 150.0 K处的晶体数据:a = 12.5777(4)的空间组P21 / c。 b = 15.2062(5),c = 21.9057(7)A,β= 95.628(3)〜0,Z = 4,R1 = 0.049。

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