首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >cis-Dioxomolybdenum(VI) complexes of a new ONN chelating thiosemicarbazidato ligand; Synthesis, characterization, crystal, molecular structures and antioxidant activities
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cis-Dioxomolybdenum(VI) complexes of a new ONN chelating thiosemicarbazidato ligand; Synthesis, characterization, crystal, molecular structures and antioxidant activities

机译:新的ONN螯合硫代氨基脲化合物的顺式-二氧钼(VI)配合物;合成,表征,晶体,分子结构和抗氧化活性

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5-Chloro-4-methyl-2-hydroxybenzophenone S-propy1-4-phenyl-thiosemicarbazone (H2L) and its cis-dioxomolybdenum(VI) complexes, in the general formula [MoO2(L)R-OH)] (R: methyl, 1; ethyl, 2; n-pro-pyl, 3; n-butyl, 4; n-pentyl, 5), were synthesized and characterized by micro analysis, electronic, infrared and H-1 and C-13 NMR spectra. The crystal structures of complexes, 1 and 3, have been solved by direct methods (SIR92) and refined to the residual indexes R-1 = 0.098 and R-1 = 0.052 respectively. Complexes 1 and 3 are crystallized in the triclinic space group P-1 with Z = 2. The crystal study of complex 1 showed the first example of intermolecular hydrogen bond for this type of molybdenum-thiosemicarbazone complexes. The hydrogen bond is between the hydroxyl proton of attached alcohol and an oxo oxygen (in MoO22+ unit) of another complex molecule, and its bond distance (1.767(1) angstrom) is shorter than from the sigma-coordination bonds in complex 1. Antioxidant activities of the compounds were determined by using 1,1-dipheny1-2-picryIhydrazyl (DPPH) method. Ligand showed 23.61% DPPH radical scavenging activity at 250 mg/L concentration. Cupric Reducing Antioxidant Capacity (CUPRAC) was also evaluated and trolox-equivalent antioxidant capacity (TEAC) values were found for ligand, 1 and 3 as 0.51, 0.33 and 0.30 respectively. (C) 2015 Elsevier B.V. All rights reserved.
机译:通式[MoO2(L)R-OH)的5-氯-4-甲基-2-羟基二苯甲酮S-propy1-4-苯基-硫代半碳酮(H2L)及其顺式-二氧钼(VI)配合物(R:合成了甲基1,乙基2,正丙基3,正丁基4,正戊基5),并通过显微分析,电子,红外和H-1和C-13 NMR谱进行了表征。配合物1和3的晶体结构已通过直接方法(SIR92)进行了解析,并分别精炼为残留指数R-1 = 0.098和R-1 = 0.052。配合物1和3在三斜空间群P-1中以Z = 2结晶。配合物1的晶体研究显示了这种类型的钼-硫代半碳酰胺配合物的分子间氢键的第一个例子。氢键在连接的醇的羟基质子与另一个复杂分子的氧代氧(以MoO22 +单元为单位)之间,并且其键距(1.767(1)埃)比在复杂物1中的sigma配位键短。化合物的活性通过1,1-二苯并1-2-甲酰基肼基(DPPH)法测定。配体在250 mg / L的浓度下显示出23.61%的DPPH自由基清除活性。还评估了铜还原抗氧化能力(CUPRAC),发现配体1和3的trolox等效抗氧化能力(TEAC)值分别为0.51、0.33和0.30。 (C)2015 Elsevier B.V.保留所有权利。

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