Cobaloxime-Catalyzed Hydrogen Evolution in Photoredox-Facilitated Small-Molecule Functionalization

被引:62
作者
Cartwright, Kaitie C. [1 ]
Davies, Alex M. [1 ]
Tunge, Jon A. [1 ]
机构
[1] Univ Kansas, Dept Chem, 1567 Irving Hill Rd, Lawrence, KS 66045 USA
基金
美国国家科学基金会;
关键词
Dehydrogenation; Hydrogen evolution; Photocatalysis; Photoredox catalysis; Synthesic methods; ACCEPTORLESS DEHYDROGENATION; ARTIFICIAL PHOTOSYNTHESIS; HOMOGENEOUS SYSTEM; H-2; EVOLUTION; H BOND; C-C; COBALT; WATER; COMPLEXES; ACTIVATION;
D O I
10.1002/ejoc.201901170
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The development of efficient, mild, economical, and low-waste processes is a cornerstone of sustainable chemistry. One such synthetic strategy that exemplifies these characteristics is the use of catalytic dehydrogenation in small-molecule functionalization. This has been achieved in recent history through the use of photoredox catalysis in conjunction with cobaloximes, a class of catalysts that are capable of proton reduction. This has allowed for a variety of bond formations to be achieved with few to no stoichiometric additives while often producing hydrogen gas as the sole stoichiometric by-product. Herein, select advancements made in this area of sustainable chemistry and catalysis are detailed and the mechanistic insights this body of work has provided thus far are evaluated. As such, this review aims to aid in the further development and study of synthetic strategies involving photoredox-promoted hydrogen evolution.
引用
收藏
页码:1245 / 1258
页数:14
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