Back Cover: Cyclic [2]Catenane Dimers, Trimers, and Tetramers (Angew. Chem. Int. Ed. 40/2015) | Zendy

Wu YiWei | Zendy; Tung ShunTe | Zendy; Lai ChienChen | Zendy; Liu YiHung | Zendy; Peng ShieMing | Zendy; Chiu ShengHsien | Zendy

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Back Cover: Cyclic [2]Catenane Dimers, Trimers, and Tetramers (Angew. Chem. Int. Ed. 40/2015)

Author(s) -

Wu YiWei,

Tung ShunTe,

Lai ChienChen,

Liu YiHung,

Peng ShieMing,

Chiu ShengHsien

Publication year - 2015

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201507436

Subject(s) - catenane , chemistry , int , covalent bond , cover (algebra) , stereochemistry , crystallography , polymer chemistry , molecule , organic chemistry , computer science , mechanical engineering , engineering , operating system

Dimeric, trimeric, and tetrameric cyclic [2]catenanes can be synthesized in a one‐pot sodium‐ion‐templated process from a diamine and a tetraaldehyde. In their Communication on page 11745 ff., S.‐H. Chiu and co‐workers describe the isolation and characterization of these oligomeric cyclic [2]catenanes as stable, covalently linked compounds after reduction and methylation.

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