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A ferrocene imidazolium-based macrocycle as an electrochemical chemosensor for halide anions

Abstract:
C4-H and C5-H protons of the imidazolium heterocycle have been exploited as a binding site for anion recognition in the design of two new redox-active imidazoliophane syn and anti isomers. The cooperative action of the two imidazolium motifs of the syn isomer is crucial for halide anion recognition. The integration of a ferrocene signalling unit at the C2 position of the imidazolium motif also facilitates the electrochemical sensing of anions by the syn isomer receptor. This journal is © the Partner Organisations 2014.
Publication status:
Published

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Publisher copy:
10.1039/c3ce41851k

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author
Publisher:
Royal Society of Chemistry
Journal:
CRYSTENGCOMM More from this journal
Volume:
16
Issue:
18
Pages:
3694-3698
Publication date:
2014-01-01
DOI:
EISSN:
1466-8033
ISSN:
1466-8033
Language:
English
Pubs id:
pubs:464204
UUID:
uuid:7fd95d1d-34e3-4455-8586-ec465cdae126
Local pid:
pubs:464204
Source identifiers:
464204
Deposit date:
2014-06-17

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