Redox and optically active carbohelicene layers prepared by potentiodynamic polymerization
| Authors | |
|---|---|
| Year of publication | 2020 |
| Type | Article in Periodical |
| Magazine / Source | Electrochemistry Communications |
| MU Faculty or unit | |
| Citation | |
| web | https://www.sciencedirect.com/science/article/pii/S1388248120300400 |
| Doi | http://dx.doi.org/10.1016/j.elecom.2020.106689 |
| Keywords | Carbohelicene; Hexahelicene; Voltammetry; Enantiopure; Redox active;Chiral carbon |
| Description | This short paper describes the preparation of thin layers based on carbohelicenes, which are inherently chiral polyaromatics existing in the enantiomeric forms P and M. Specifically, [5], [6] and [7]helicene were subjected to redox cycling between -1.5 and 1.5 V vs. ferrocene/ferrocenium at a scan rate of 10 V/s. This way, enantiopure layers exhibiting redox activity were formed on the surfaces of the glassy carbon and ITO electrodes under anoxic and non-aqueous conditions. The properties of the prepared polymer layers were investigated using electrochemistry with Fe/Ru redox probes, circular dischroism, AFM, impedance measurement and Raman spectroscopy. With [6]helicene, the suggested electropolymerization procedure thus represents a proof-of-concept for the preparation of chiral carbonaceous surfaces. |
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