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  4. Electrochemically Controlled Proton-Transfer-Catalyzed Reactions at Liquid-Liquid Interfaces: Nucleophilic Substitution on Ferrocene Methanol
 
research article

Electrochemically Controlled Proton-Transfer-Catalyzed Reactions at Liquid-Liquid Interfaces: Nucleophilic Substitution on Ferrocene Methanol

Peljo, Pekka  
•
Qiao, Liang  
•
Murtomäki, Lasse
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2013
ChemPhysChem

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.

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Type
research article
DOI
10.1002/cphc.201200953
Web of Science ID

WOS:000314169100018

Author(s)
Peljo, Pekka  
Qiao, Liang  
Murtomäki, Lasse
Johans, Christoffer
Girault, Hubert H.  
Kontturi, Kyösti
Date Issued

2013

Publisher

Wiley-Blackwell

Published in
ChemPhysChem
Volume

14

Issue

2

Start page

311

End page

314

Subjects

carbocations

•

electrochemistry

•

liquid–liquid interfaces

•

nucleophilic substitutions

•

proton transfer

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LEPA  
Available on Infoscience
January 31, 2013
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/88448
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