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Chem Commun (Camb) ; 56(44): 5993-5996, 2020 Jun 04.
Artigo em Inglês | MEDLINE | ID: mdl-32347845

RESUMO

Incorporation of azobenzene into the linker of bimetallic chiral salen TiIV catalysts allowed the photoswitchable arrangement of the two Ti(salen) units through cis/trans photoisomerization of azobenzene. The differently arranged Ti(salen) units changed their cooperative function to reflect the positional relationships, as a result, their efficiency as cooperative catalysts in asymmetric sulfoxidation could be readily controlled by light stimuli.

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