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Synthesis and Electrochemical Properties of Two Transition Metal Coordination Complexes Based on 4-Pyridyl-Substituted TTF Ligand

机译:基于4-吡啶基取代的TTF配体的两种过渡金属配位化合物的合成及电化学性能

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摘要

The synthesis, crystal structures, and electrochemical properties of two transition metal coordination complexes, Co(acac)(2)center dot(EDO-TTF-4-py)(2)center dot 2CH(3)CN 1, and ZnBr2 center dot(EDO-TTF-4-py)(2) 2, are reported, where acac = acetylacetonate and EDO-TTF-4-py, L1 (EDO-TTF = ethylenedioxotetrathiafulvalene; py = pyridine). In complex 1, two N atoms from L1 are coordinated in the trans configuration to the Co(II) ion of Co(acac)(2) to form an octahedral Co complex. And in complex 2, the Zn(II) atom is tetrahedral by two N atoms from L1 and two Br ions. Cyclic voltammetry measurements for both complexes show a sizable interaction involving the electroactive L1 ligand and the metal ion.
机译:两种过渡金属配位化合物Co(acac)(2)中心点(EDO-TTF-4-py)(2)中心点2CH(3)CN 1和ZnBr2中心点的合成,晶体结构和电化学性质(EDO-TTF-4-py)(2)2,据报道,其中acac =乙酰丙酮酸酯和EDO-TTF-4-py,L1(EDO-TTF =乙二氧基四硫杂富瓦烯; py =吡啶)。在络合物1中,来自L1的两个N原子以反式构型与Co(acac)(2)的Co(II)离子配位,形成八面体Co络合物。在络合物2中,Zn(II)原子被来自L1和两个Br离子的两个N原子四面体化。两种复合物的循环伏安法测量均显示涉及电活性L1配体和金属离子的大量相互作用。

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