Journal article
A [2]catenane displaying pirouetting motion triggered by debenzylation and locked by chloride anion recognition.
- Abstract:
- Chloride locks the rings: Debenzylation of a chloride-templated N-benzyl pyridinium catenane, allows for a 180° "pirouetting" of the rings in the resulting neutral pyridyl catenane (see scheme). The catenane may be returned to its original co-conformation by chloride recognition as evidenced in solution and in the solid state. Copyright © 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim.
- Publication status:
- Published
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- Publisher copy:
- 10.1002/chem.201101033
Authors
- Journal:
- Chemistry (Weinheim an der Bergstrasse, Germany) More from this journal
- Volume:
- 17
- Issue:
- 28
- Pages:
- 7734-7738
- Publication date:
- 2011-07-01
- DOI:
- EISSN:
-
1521-3765
- ISSN:
-
0947-6539
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:141487
- UUID:
-
uuid:00f98164-5eaf-4185-bbbd-720650d22026
- Local pid:
-
pubs:141487
- Source identifiers:
-
141487
- Deposit date:
-
2012-12-19
- ARK identifier:
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- Copyright date:
- 2011
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