Direct conversion of  CO 2   with diols, aminoalcohols and diamines to cyclic carbonates, cyclic carbamates and cyclic ureas using heterogeneous catalysts | Zendy

Tamura Masazumi | Zendy; Honda Masayoshi | Zendy; Nakagawa Yoshinao | Zendy; Tomishige Keiichi | Zendy

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Direct conversion of CO 2 with diols, aminoalcohols and diamines to cyclic carbonates, cyclic carbamates and cyclic ureas using heterogeneous catalysts

Author(s) -

Tamura Masazumi,

Honda Masayoshi,

Nakagawa Yoshinao,

Tomishige Keiichi

Publication year - 2014

Publication title -

journal of chemical technology and biotechnology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.64

H-Index - 117

eISSN - 1097-4660

pISSN - 0268-2575

DOI - 10.1002/jctb.4209

Subject(s) - catalysis , chemistry , greenhouse gas , organic chemistry , combinatorial chemistry , biology , ecology

CO 2 has a large effect on global warming by greenhouse gases, and development of an effective technique for the reduction of CO 2 is a crucial and urgent issue. From the chemical viewpoint, CO 2 is regarded as a stable, safe and abundant C1 resource, and the transformation of CO 2 to valuable chemicals is promising not only for reduction of CO 2 but also for production of useful chemicals. This mini‐review focuses on the direct conversion of CO 2 with diols, aminoalcohols and diamines to cyclic compounds such as cyclic carbonates, cyclic carbamates and cyclic ureas, and in particular discusses the mechanisms for these reactions over heterogeneous catalysts. © 2013 Society of Chemical Industry

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