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Laboratoire d'Electrochimie Moleculaire, LEM, Paris

UMR CNRS - Université de Paris - Paris France

   
 
Master Frontiers in Chemistry | UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie Université de Paris Master Chimie Sorbonne Paris Cité UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie Master Frontiers in Chemistry | UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie Université de Paris Master Chimie Sorbonne Paris Cité UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie
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Chimie - Université de Paris
Université de Paris - Accueil CNRS - Centre national de la recherche scientifique Université de Paris | Faculté des Sciences
 
 


Le LEM - Publications: Abstracts

Publication 907

Chem. Commun., 56, 7491-7494, 2020
DOI:10.1039/D0CC02604B
   
doi

Precious-metal free photocatalytic production of an NADH analogue using cobalt diimine–dioxime catalysts under both aqueous and organic conditions

Chun-Leung Kwok, Shun-Cheung Cheng, Pui-Yu Ho, Shek-Man Yiu, Wai-Lun Man, Vonika Ka-Man Au, Po-Keung Tsang, Chi-Fai Leung, Chi-Chiu Ko, and Marc Robert

Department of Science and Environmental Studies, The Education University of Hong Kong, 10 Lo Ping Road, Tai Po, New Territories, Hong Kong, China
Department of Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China
Department of Chemistry, Hong Kong Baptist University, Waterloo Road, Kowloon, Hong Kong
Université de Paris, Laboratoire d’Electrochimie Moléculaire, CNRS, F-75013 Paris, France
Institut Universitaire de France (IUF), F-75005 Paris, France


The photocatalytic generation of an NADH synthetic analogue, i.e. 1-benzyl-1,4-dihydronicotinamide (1,4-BNAH), has been studied using the cobalt diimino-dioxime complexes and the BF2-bridged derivative as catalysts. 1,4-BNAH was produced in both aqueous and organic media at unprecedented turnover numbers with metal and organic photosensitizers, respectively.

 
   
 
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