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Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
1,5,9,13-Tetraselena[13]ferrocenophane: synthesis, complexation, crystallographic and electrochemical study
Su Jing1, Christopher P Morley, Cheng-Yun Gu
1School of Science, Nanjing University of Technology, Nanjing, 210009, PR China. sjing@njut.edu.cn
Abstract:
A novel macrocyclic ferrocenophane, 1,5,9,13-tetraselena[13]ferrocenophane (L), was synthesized. Reaction of L with [M(NCMe)(4)](PF(6))(2) (M = Pd and Pt) or [Cu(NCMe)(4)](PF(6)) led to complexes [ML](PF(6))(2) (M = Pd and Pt) or [CuL](PF(6)). The Ag(i) cation induced the formation of a one-dimensional polymer {[AgL](PF(6))}(n) due to its large ionic radius. The structures of L and its four complexes have been determined by X-ray crystallography. Electrochemical studies showed that, in [ML](PF(6))(2) (M = Pd and Pt), the half-wave potential of the 1,1'-ferrocenediyl group shifts to much more positive potentials due to the strong through-space interaction between the two metals (M...Fe).
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