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Synthesis, characterization, DFT and Td-dfT study of the [Fe(mnt)(L)(t-BuNC) 2] octahedral complex (L = phen, bipy)

机译:[Fe(mnt)(L)(t-BuNC)2]八面体络合物(L = phen,bipy)的合成,表征,DFT和Td-dfT研究

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摘要

FeBr2 has reacted with an equivalent of mnt2- (mnt = cis-1,2-dicyanoethylene-1,2-dithiolate) and the α-diimine L (L = 1,10'-phenantroline, 2,2'-bipyridine) in THF solution, and followed by adding of t-butyl-isocyanide to give [Fe(mnt)(L)(t-BuNC)2] neutral compound. The products were characterized by infrared, UV-visible and Mössbauer spectroscopy, besides thermogravimetric and conductivity data. The geometry in the equilibrium was calculated by the density functional theory and the electronic spectrum by the time-dependent. The experimental and theoretical results in good agreement have defined an octahedral geometry with two isocyanide neighbours. The π→π* intraligand electronic transition was not observed for cis-isomers in the near-IR spectral region.
机译:FeBr2与当量的mnt2-(mnt =顺式1,2-二氰基乙烯-1,2-二硫代酸酯)和α-二亚胺L(L = 1,10'-菲咯啉,2,2'-联吡啶)反应在THF溶液中,然后加入叔丁基异氰酸酯,得到[Fe(mnt)(L)(t-BuNC)2]中性化合物。除热重和电导率数据外,产品还通过红外,紫外可见和穆斯堡尔光谱法进行表征。平衡中的几何结构是通过密度泛函理论计算的,而电子光谱则是随时间变化的。实验和理论结果吻合良好,定义了一个具有两个异氰酸酯邻域的八面体几何形状。在近红外光谱范围内未观察到顺式异构体的π→π*配体电子跃迁。

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