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A Conjugated Covalent Template Strategy for All‐Benzene Catenane Synthesis.
- Source :
- Angewandte Chemie International Edition; 9/26/2022, Vol. 61 Issue 39, p1-5, 5p
- Publication Year :
- 2022
-
Abstract
- Mechanically interlocked molecules based on oligoparaphenylene‐derived nanohoops, particularly those without heteroatoms, are synthetically challenging and topologically intriguing targets. Herein, a π‐conjugated covalent template strategy based on azo group has been developed, which features dual intramolecular macrocyclizations directed by a tetra‐substituted azobenzene core, followed by traceless removal of the azo linker. Employing this strategy, the efficient synthesis of a novel all‐benzene [2]catenane consisting of meta‐cycloparaphenylenes has been accomplished. [ABSTRACT FROM AUTHOR]
- Subjects :
- AZOBENZENE
MOLECULES
Subjects
Details
- Language :
- English
- ISSN :
- 14337851
- Volume :
- 61
- Issue :
- 39
- Database :
- Complementary Index
- Journal :
- Angewandte Chemie International Edition
- Publication Type :
- Academic Journal
- Accession number :
- 159193749
- Full Text :
- https://doi.org/10.1002/anie.202209449