Oxiranes and carbon dioxide are known to cycloadd and/or copolymerize
in the presence of a variety of catalysts. Indeed, cyclic carbonates a
re prepared on a technical scale by coupling epoxides and carbon dioxi
de. The fact that cyclic carbonate formation represents one of the few
examples of successful carbon dioxide utilization, coupled with the h
igh reactivity of epoxides, has resulted in many papers which reveal a
remarkable variety of active catalysts for the CO2/epoxide coupling p
rocesses. Catalysts include simple alkali metal salts, ammonium salts,
phosphines, main-group metal complexes, and both non-oxidative and ox
idative transition-metal complexes. The purpose of this review is to c
ompile the different catalysts into their general groups of similarity
, with the hopes of shedding light on some of the important difference
s in reaction pathways. There generally appears to be a lack of detail
ed mechanistic studies; therefore, it is hoped that this review will e
mphasize where mechanistic clarification is most importantly needed. F
urthermore, we anticipate that this review will provide insight into c
yclic carbonate vs. poIycarbonate production from the CO2/epoxide coup
ling process.