research article
Electrochemically Controlled Proton-Transfer-Catalyzed Reactions at Liquid-Liquid Interfaces: Nucleophilic Substitution on Ferrocene Methanol
2013
The generation of α-ferrocenyl carbocations from ferrocenyl alcohols for SN1 substitution at the water–organic solvent interface is initiated by the transfer of protons into the organic phase. The proton flux, and hence the reaction rate, can be controlled by addition of a suitable “phase-transfer catalyst” anion or by external polarization with a potentiostat, providing a new method for the synthesis of ferrocene derivatives.
Type
research article
Web of Science ID
WOS:000314169100018
Author(s)
Date Issued
2013
Publisher
Published in
Volume
14
Issue
2
Start page
311
End page
314
Editorial or Peer reviewed
REVIEWED
Written at
EPFL
EPFL units
Available on Infoscience
January 31, 2013
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