Abstract

Self-assemblies of the flexible ferrocenyl block 2-chloro-4-ferrocenylbenzoate with Cd2+ cations in the presence of N-containing auxiliary ligand result in two coordination complexes, namely, &{[Cd(η2 -OOCClH3C6Fc)2(Mbbz)(CH3OH)] · (H2O)0.5} n (I) and [Cd(η2 -OOCClH3C6Fc)2(Bbbm)] n (II) {Fc = (η5- C5H4)Fe(η5-C5H4), Mbbz = 1,1'-methyl benzimidazole, Bbbm = 1,4-bis(benzimidazol-1-ylmethyl)-benzene}. Their structure has been determined by single-crystal X-ray diffraction analyses (CIF files nos. 1529095 (I), 1529096 (II)) and further characterized by elemental analyses, IR spectra, and thermogravimetric analyses. Crystallographic characterization shows that both I and II are 1D chain structures. Notably, various C–H···π interactions and C–H···Cl interactions are discovered in I and II, and they have significant contributions to self-assembly, which extend 1D complex to infinite 3D supramolecular networks. Moreover, the electrochemical studies of I and II in DMF solution display irreversible redox waves and indicate that the half-wave potentials of the ferrocenyl moieties in I and II are shifted to positive potential compared with that of free 2-chloro-4-ferrocenylbenzoate.

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