| Literature DB >> 30601601 |
Yang Hu1, Kai Lang2, Jingran Tao1, McKenzie K Marshall1, Qigan Cheng1, Xin Cui1, Lukasz Wojtas1, X Peter Zhang2.
Abstract
Novel D2 -symmetric chiral amidoporphyrins with alkyl bridges across two chiral amide units on both sides of the porphyrin plane (designated "HuPhyrin") have been effectively constructed in a modular fashion to permit variation of the bridge length. The CoII complexes of HuPhyrin, [Co(HuPhyrin)], represent new-generation metalloradical catalysts where the metal-centered d-radical is situated inside a cavity-like ligand with a more rigid chiral environment and enhanced hydrogen-bonding capability. As demonstrated with cyclopropanation and aziridination as model reactions, the bridged [Co(HuPhyrin)] functions notably different from the open catalysts, exhibiting significant enhancement in both reactivity and stereoselectivity. Furthermore, the length of the distal alkyl bridge can have a remarkable influence on the catalytic properties.Entities:
Keywords: chiral porphyrinoids; cobalt; ligand design; metalloradical catalysis; synthetic methods
Year: 2019 PMID: 30601601 PMCID: PMC6456056 DOI: 10.1002/anie.201812379
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336