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- W2577573764 abstract "Two novel ferrocene organometallic complexes of [Mn(C16H16FeN2O2)4(H2O)2]Cl2 1 and [Co(C16H16FeN2O2)4(H2O)2](NO3)2·3H2O 2 were synthesized under solvothermal conditions and characterized by IR spectroscopy, elemental analyses, and thermogravimetric analyses. Single-crystal X-ray diffraction analyses revealed that the two complexes were centrosymmetric species with the central atom in six-coordinated environment. Interestingly, supramolecular constructions of 1 and 2 are totally different due to intriguing hydrogen-bonded systems. Complex 1 was dominated by non-classical CH⋯O hydrogen bonds while 2 was assembled by both classical OH⋯O hydrogen bonds and CH⋯O hydrogen bonds. Different from chloride ions only balanced the electric charge in 1, nitrate anions in 2 not only balanced the electric charge but also contributed largely to stability through OH⋯O hydrogen bonds. Electrochemical investigation revealed that both 1 (ΔEp = 189 mV, Ipa/Ipc = 1.32) and 2 (ΔEp = 95 mV, Ipa/Ipc = 0.96) displayed anticipated one-electron redox process of the ferrocenyl group. Moreover, complex 2 had better redox reversibility than 1. Furthermore, UV–Vis absorption spectrum has been applied to prove the stability of complex ions of [Mn(C16H16FeN2O2)4(H2O)2]2+ and [Co(C16H16FeN2O2)4(H2O)2]2+ in acetonitrile for better understanding of electrochemical investigation. It’s significant to reveal the structural and electrochemical characters of these kind of ferrocene-containing complexes for the further application on areas of anticancer metallodrugs based on their good redox-activity." @default.
- W2577573764 created "2017-01-26" @default.
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- W2577573764 date "2017-04-01" @default.
- W2577573764 modified "2023-09-25" @default.
- W2577573764 title "Mn(II) and Co(II) complexes functionalized by imidazolyl-ferrocene: Electrochemical property and different supramolecular architectures driven by intriguing hydrogen-bonded system" @default.
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- W2577573764 doi "https://doi.org/10.1016/j.poly.2017.01.016" @default.
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