Fine-Tuning Conformational Motion of a Self-Assembled Metal-Organic Macrocycle by Multiple CH⋅⋅⋅Anion Hydrogen Bonds
Anion switches: A bistable self‐assembled metal–organic macrocycle undergoes intramolecular conformational motion that is switched reversibly with anions by multiple hydrogen‐bonding interactions (see picture; Pd orange, N blue, O red). The molecular bowl fixed with a nitrate anion could be freed to...
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Published in | Angewandte Chemie International Edition Vol. 51; no. 5; pp. 1177 - 1181 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
27.01.2012
WILEY‐VCH Verlag |
Subjects | |
Online Access | Get full text |
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Summary: | Anion switches: A bistable self‐assembled metal–organic macrocycle undergoes intramolecular conformational motion that is switched reversibly with anions by multiple hydrogen‐bonding interactions (see picture; Pd orange, N blue, O red). The molecular bowl fixed with a nitrate anion could be freed to a partial chair by adding a tetraphenylborate anion. |
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Bibliography: | ArticleID:ANIE201106504 Beijing Natural Science Foundation - No. 2112018 National Natural Science Foundation of China - No. 91127039; No. 51073171; No. 21025207 The Fundamental Research Funds for the Central Universities istex:426EEDE9FE5E7CB437BA8120E4A33C5B325E7A63 ark:/67375/WNG-NMGCRLRK-B This project was supported by The Fundamental Research Funds for the Central Universities, and the Research Funds of Renmin University of China (No. 11XNL011), the National Natural Science Foundation of China (No. 91127039, 51073171, 21025207), and the Beijing Natural Science Foundation (No. 2112018). Research Funds of Renmin University of China - No. 11XNL011 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201106504 |