Photoredox catalysts based on earth-abundant metal complexes

被引:219
|
作者
Hockin, Bryony M. [1 ,2 ]
Li, Chenfei [1 ]
Robertson, Neil [2 ]
Zysman-Colman, Eli [1 ]
机构
[1] Univ St Andrews, EaStCHEM Sch Chem, Organ Semicond Ctr, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Edinburgh, EaStCHEM Sch Chem, Edinburgh EH9 3FJ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; TRANSFER RADICAL-ADDITION; VISIBLE-LIGHT PHOTOCATALYSIS; TRANSFER EXCITED-STATES; DIELS-ALDER REACTIONS; COPPER(I) COMPLEXES; CU(I) COMPLEXES; BOND-CLEAVAGE; PHOTOPHYSICAL PROPERTIES; MEDIATED SYNTHESIS;
D O I
10.1039/c8cy02336k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Over the last decade, visible light photoredox catalysis has exploded into the consciousness of the synthetic chemist. The principal photocatalysts used are based on rare and toxic ruthenium(ii) and iridium(iii) complexes. This critical review focusses on Earth-abundant metal complexes as potential replacement photocatalysts and summarizes the use of photoactive Cu(i), Zn(ii), Ni(0), V(v), Zr(iv), W(0), W(vi), Mo(0), Cr(iii), Co(iii) and Fe(ii) complexes in photoredox reactions. The optoelectronic properties of these complexes and relevant structurally related analogs, not yet used for photoredox catalysis, are discussed in combination with the reaction scope reported for each photocatalyst. Prospects for the future of photocatalyst design are considered.
引用
收藏
页码:889 / 915
页数:27
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