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Designed molecular switches: controlling the conformation of benzamido-diphenylacetylenes.

Abstract:
With the goal of creating a molecular switch, the hydrogen-bonded diphenylacetylene structure has been modified such that an equilibrium now exists between two intramolecular H-bonded states. Through X-ray crystallography and (1)H NMR analysis it is shown that this equilibrium can be biased in a predictable manner by modulating the relative acidity of the amide NH's.
Publication status:
Published

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Publisher copy:
10.1021/ol101397y

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Journal:
Organic letters More from this journal
Volume:
12
Issue:
16
Pages:
3651-3653
Publication date:
2010-08-01
DOI:
EISSN:
1523-7052
ISSN:
1523-7060
Language:
English
Pubs id:
pubs:117495
UUID:
uuid:22c2595c-c135-45f0-9ff6-6769d9198a7b
Local pid:
pubs:117495
Source identifiers:
117495
Deposit date:
2012-12-19

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