Catenane organocatalyst breaks the linear scaling limitation through conformational selection
Conformational dynamics are integral to enzyme catalysis, yet they are barely explored when designing synthetic catalysts. Now, a catenane-based organocatalyst, which dynamically switches between two conformations, speeds up the catalysis of carbodiimide hydration through spontaneous conformational...
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Published in | Communications chemistry Vol. 7; no. 1; p. 9 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
08.01.2024
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Conformational dynamics are integral to enzyme catalysis, yet they are barely explored when designing synthetic catalysts. Now, a catenane-based organocatalyst, which dynamically switches between two conformations, speeds up the catalysis of carbodiimide hydration through spontaneous conformational adaptation for different reaction steps. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2399-3669 2399-3669 |
DOI: | 10.1038/s42004-023-01088-w |