Issue 26, 2015

Dual catalysis with magnetic chitosan: direct synthesis of cyclic carbonates from olefins with carbon dioxide using isobutyraldehyde as the sacrificial reductant

Abstract

Chitosan coated magnetic nanoparticles were synthesized and used as a support for the immobilization of the cobalt(II) acetylacetonate complex [Co(acac)2] and quaternary triphenylphosphonium bromide [P+Ph3Br] targeting –NH2 and –OH moieties located on the surface of chitosan. The synthesized material was used as a catalyst for one pot direct synthesis of cyclic carbonates from olefins via an oxidative carboxylation approach with carbon dioxide using isobutyraldehyde as the sacrificial reductant and molecular oxygen as the oxidant. After the reaction, the catalyst was recovered by applying an external magnet and reused for several runs without significant loss in catalytic activity and no leaching was observed during this course.

Graphical abstract: Dual catalysis with magnetic chitosan: direct synthesis of cyclic carbonates from olefins with carbon dioxide using isobutyraldehyde as the sacrificial reductant

Supplementary files

Article information

Article type
Paper
Submitted
13 Mar 2015
Accepted
21 May 2015
First published
21 May 2015

Dalton Trans., 2015,44, 11860-11866

Dual catalysis with magnetic chitosan: direct synthesis of cyclic carbonates from olefins with carbon dioxide using isobutyraldehyde as the sacrificial reductant

S. Kumar, N. Singhal, R. K. Singh, P. Gupta, R. Singh and S. L. Jain, Dalton Trans., 2015, 44, 11860 DOI: 10.1039/C5DT01012H

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