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Facile synthesis of a chiral ionic liquid derived from 1-Phenylethylamine

journal contribution
posted on 2024-11-16, 06:20 authored by Syed Ashraf, Gordon WallaceGordon Wallace, Leon Kane-Maguire, Yingpit Pornputtkul
A simple route is described to enantiomerically pure ionic liquids derived from (+)- and (–)-1-phenylethylamine. These very low melting point (–42°C) ionic liquids, containing the bis(trifluoromethylsulfonylimide) anion, possess a wide electrochemical potential window between –2.0 and +2.0 V (versus Ag|AgCl). They show chiral discrimination between the enantiomeric forms of Mosher’s salt, suggesting their potential as media for electrochemical asymmetric syntheses or chiral chromatography.

Funding

Nanobionics

Australian Research Council

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History

Citation

Ashraf, S. A., Pornputtkul, Y., Kane-Maguire, L. A. & Wallace, G. G. (2007). Facile synthesis of a chiral ionic liquid derived from 1-Phenylethylamine. Australian Journal of Chemistry: an international journal for chemical science, 60 64-67.

Journal title

Australian Journal of Chemistry

Volume

60

Issue

1

Pagination

64-67

Publisher website/DOI

Language

English

RIS ID

22896

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