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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis, EPR and Mossbauer spectral studies of new iron(III) complexes with 2-benzoylpyridine-N(4), N(4)-(butane-1,4-diyl) thiosemicarbazone (HBpypTsc): X-ray structure of [Fe(BpypTSC)2]FeCl4 center dot 2H(2)O and the free ligand
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Synthesis, EPR and Mossbauer spectral studies of new iron(III) complexes with 2-benzoylpyridine-N(4), N(4)-(butane-1,4-diyl) thiosemicarbazone (HBpypTsc): X-ray structure of [Fe(BpypTSC)2]FeCl4 center dot 2H(2)O and the free ligand

机译:新的铁(III)与2-苯甲酰基吡啶-N(4),N(4)-(丁烷-1,4-二基)硫代半脲(HBpypTsc)的新铁(III)配合物的合成,EPR和莫斯鲍尔光谱研究:[Fe的X射线结构(BpypTSC)2] FeCl4中心点2H(2)O和自由配体

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摘要

Three novel iron(III) complexes of 2-benzoylpyridine N(4), N(4)-(butyl-1,4-diyl) thiosemicarbazone (HBpypTsc), [Fe(BpypTsc)(2)]ClO4 (1), [Fe(BpypTsc)(2)]NO3 (2) and [Fe(BpypTSC)(2)]FeCl4 (3) were synthesized and physico-chemically characterized by means of partial elemental analyses, magnetic measurements (polycrystalline state), UV-Vis and IR spectroscopies. The spin Hamiltonian parameters, isomer shifts and quadrupolar splitting values of the complexes were assigned by variable temperature EPR and Mossbauer spectra. The presence of a spin-paired iron(Ill) cation with d(xz)(2)d(yz)(2)d(xy)(1), ground state is revealed by the simulated EPR spectral data. The structures of the free ligand HBpypTsc and one of the complexes [Fe(BpypTsc)(2)]FeCl4 (3) were solved by single crystal X-ray diffraction which authenticated a FeN4S2 octahedral coordination in the complex, as envisaged from the spectral data. All complexes except [Fe(BpypTsc)(2)]FeCl4 (3) were found to be low-spin S = 1/2 (T-2(2g)), whereas 3 was found to have both low-spin (T-2(2g)) and high-spin ((6)A(1)) centres. (C) 2004 Elsevier Ltd. All rights reserved.
机译:三个新的铁(III)配合物的2-苯甲酰基吡啶N(4),N(4)-(丁基-1,4-二基)硫代半脲(HBpypTsc),[Fe(BpypTsc)(2)] ClO4(1),[ Fe(BpypTsc)(2)] NO3(2)和[Fe(BpypTSC)(2)] FeCl4(3)的合成和理化特性通过部分元素分析,磁测量(多晶态),UV-Vis和红外光谱。通过可变温度EPR和Mossbauer光谱指定了自旋哈密顿参数,配合物的异构体位移和四极分裂值。通过模拟的EPR光谱数据揭示了具有d(xz)(2)d(yz)(2)d(xy)(1)基态的自旋配对的铁(III)阳离子的存在。游离配体HBpypTsc和一种配合物[Fe(BpypTsc)(2)] FeCl4(3)的结构通过单晶X射线衍射解决,该光谱通过光谱数据验证了该配合物中FeN4S2八面体的配位身份。除[Fe(BpypTsc)(2)] FeCl4(3)外,所有配合物均为低旋S = 1/2(T-2(2g)),而3个均具有低旋(T- 2(2g))和高旋转((6)A(1))中心。 (C)2004 Elsevier Ltd.保留所有权利。

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