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Oxidovanadium(IV) complexes containing ligands derived from dithiocarbazates _ Models for the interaction of VO2+ with thiofunctional ligands

机译:含衍生自二硫代氨基甲酸酯的配体的氧化钒(IV)配合物_VO2 +与硫官能配体相互作用的模型

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The tetragonal_pyramidal VO2+ complexes [VO{(RSC_S)@N_N@X}2] (1_6) were synthesised by the reactions of VO(OCHMe2)3 with the dithiocarbazate ligands RSC(@S)_NH_N@X, where X = cyclo-pentyl, cyclohexyl or 4-Me2N_C6H4_CH, and R = CH3 or CH2C6H5. The compounds were characterised by elemental analysis, IR- and mass spectrometries, and in cases of compounds 1, 3, 4 and 5, by X-ray diffraction. The chiral compound 4 (X = cyclo-hexyl, R = CH2C6H5) crystallises in the C configuration. In compound 5, the V@O moiety is disordered (83.3:16.7%) with respect to the plane spanned by the four equatorial ligand functions.
机译:通过VO(OCHMe2)3与二硫代氨基甲酸酯配体RSC(@S)_NH_N @ X的反应合成四方锥体的VO2 +络合物[VO {(RSC_S)@ N_N @ X} 2](1_6),其中X =环戊基,环己基或4-Me2N_C6H4_CH,且R = CH3或CH2C6H5。通过元素分析,红外光谱和质谱对化合物进行表征,对于化合物1、3、4和5,则通过X射线衍射对其进行表征。手性化合物4(X =环己基,R = CH 2 C 6 H 5)以C构型结晶。在化合物5中,相对于由四个赤道配体官能团跨越的平面,V O部分是无序的(83.3:16.7%)。

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