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Anion-Binding-Induced Electrochemical Signal Transduction in Ferrocenylimidazolium: Combined Electrochemical Experimental and Theoretical Investigation

Five ferrocene alkymethylimidazolium cations 1a–1d and 2 with different alkyl spacer lengths were reinvestigated using voltammetry and density functional theory (DFT) calculations. The voltammetric responses of ligand 2 toward various anions are described in detail. An interesting and unprecedented...

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Detalles Bibliográficos
Autores principales: Weng, Tan-Qing, Huang, Yi-Fan, Xue, Lou-Sha, Cheng, Jie, Jin, Shan, Liu, Sheng-Hua, Wu, De-Yin, Chen, George Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359666/
https://www.ncbi.nlm.nih.gov/pubmed/30634644
http://dx.doi.org/10.3390/molecules24020238
Descripción
Sumario:Five ferrocene alkymethylimidazolium cations 1a–1d and 2 with different alkyl spacer lengths were reinvestigated using voltammetry and density functional theory (DFT) calculations. The voltammetric responses of ligand 2 toward various anions are described in detail. An interesting and unprecedented finding from both experimental and theoretical studies is that coupled electron and intramolecular anion (F(−)) transfer may be present in these molecules. In addition, it was also observed that, in these studied molecules, the electrostatic attraction interaction toward F(−) would effectively vanish beyond 1 nm, which was previously reported only for cations.