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Synthesis, characterization and DFT studies of the cobalt(III) complex of a tetrapodal pentadentate N4S donor ligand

机译:四足五齿N4S供体配体的钴(III)配合物的合成,表征和DFT研究

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摘要

The synthesis of the pentadentate ligand 2,6-bis(3,3-dimethyl-2,4-dioxocyclohexanyl)-4-thiaheptane (N(4)Samp) is described. The synthetic pathway involves the coupling of two 1,3-(dimethylenedioxy)-2-methyl-2-(methylene-p-toluenesulfonyl)propane moieties with sodium sulfide and subsequent synthetic elaboration to prepare the final N4S donor system. The cobalt(III) complex [Co(N(4)Samp)Cl](2+) has been prepared and subsequently crystallized as the tetrachlorozincate salt. The X-ray structure analysis confirms the pentadentate nature of the ligand and shows the thioether donor occupying one apex with four equivalent amine donors effectively occupying the equatorial plane of the molecule. The sixth coordination site is occupied by a chloro ligand. The electronic absorption and C-13 NMR spectra have been studied. DFT calculations have been employed to explore structural and mechanistic comparisons between [Co(N(4)Samp)Cl](2+) and an analogous pentaamine complex.
机译:描述了五齿配体2,6-双(3,3-二甲基-2,4-二氧代环己基)-4-硫庚烷(N(4)Samp)的合成。合成途径涉及将两个1,3-(二甲基二氧基)-2-甲基-2-(亚甲基-对甲苯磺酰基)丙烷部分与硫化钠偶联,然后进行合成修饰,以制备最终的N4S供体体系。制备了钴(II​​I)配合物[Co(N(4)Samp)Cl](2+),随后结晶为四氯锌酸盐。 X射线结构分析证实了配体的五齿性质,并表明硫醚供体占据一个顶点,而四当量胺供体有效占据分子的赤道面。第六配位位点被氯配体占据。已经研究了电子吸收和C-13 NMR谱。 DFT计算已用于探索[Co(N(4)Samp)Cl](2+)与类似五胺配合物的结构和机理比较。

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