Metal-carboxylate coordination polymers with redox-active moiety of tetrathiafulvalene (TTF)

摘要

Though numerous metal-organic frameworks or polymers have been reported, the organic building blocks are usually not redox-active. On the other hand, some mono-, di- or tri-nuclear compounds with tetrathiafulvalene (TTF) have been prepared, although little is known about the coordination polymers combined with paramagnetic metals and organic TTF ligands. We report herein a series of coordination polymers of copper(ii) and manganese(ii) with TTF dicarboxylate ligand (L). Compound 1, [CuL(2,2-bpy)]_n, is a one-dimensional (1-D) coordination polymer with five-coordinated square-pyramidal Cu(ii) centers. Mn(ii) complex 2, [MnL(2,2-bpy)]_n, also takes a 1-D structure, showing a double-bridged mode by carboxylate groups. The 4,4-bipyridine compound 3, [MnL(4,4-bpy)(H_2O)]_n·CH_3CN, takes a 2-D grid network. A zinc(ii) compound 4, [ZnL(4,4-bpy)(H_2O)] _n·CH_3CN, isomorphous structure with 3, is also presented. The electrochemical properties of the solid-state compounds were investigated by cyclic voltammetry using surface-modified electrodes. As usually observed in TTF derivatives, two sets of redox-waves were observed. The values of E_(1/2)(1) of compounds 1-4 are in the order of 2(Mn) ≈ 3(Mn) < 1(Cu) < 4(Zn), indicating that the metal coordination can affect the potential shift of the TTF ligand. Weak antiferromagnetic exchanges are observed for compounds 1, 2, and 3.