Issue 6, 2014

Nucleophile-directed selectivity towards linear carbonates in the niobium pentaethoxide-catalysed cycloaddition of CO2 and propylene oxide

Abstract

Homoleptic Nb-complexes combined with selected organic nucleophiles generate very active catalytic systems for the cycloaddition of propylene oxide and CO2 under ambient conditions. An unprecedented reaction pathway towards an acyclic organic carbonate is observed when extending the study to [Nb(OEt)5] in combination with 4-dimethylamino-pyridine (DMAP) or tetra-n-butylammonium bromide (TBAB). Mechanistic insights of the reaction are provided based on experimental and spectroscopic evidences.

Graphical abstract: Nucleophile-directed selectivity towards linear carbonates in the niobium pentaethoxide-catalysed cycloaddition of CO2 and propylene oxide

Supplementary files

Article information

Article type
Communication
Submitted
02 Jan 2014
Accepted
01 Mar 2014
First published
03 Mar 2014

Catal. Sci. Technol., 2014,4, 1534-1538

Author version available

Nucleophile-directed selectivity towards linear carbonates in the niobium pentaethoxide-catalysed cycloaddition of CO2 and propylene oxide

B. Dutta, J. Sofack-Kreutzer, A. A. Ghani, V. D'Elia, J. D. A. Pelletier, M. Cokoja, F. E. Kühn and J. Basset, Catal. Sci. Technol., 2014, 4, 1534 DOI: 10.1039/C4CY00003J

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