Nucleophile-directed selectivity towards linear carbonates in the niobium pentaethoxide-catalysed cycloaddition of CO 2 and propylene oxide

Citation data:

Catal. Sci. Technol., ISSN: 2044-4753, Vol: 4, Issue: 6, Page: 1534-1538

Publication Year:
2014
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Citations 20
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Repository URL:
http://hdl.handle.net/10754/563198
DOI:
10.1039/c4cy00003j
Author(s):
Dutta, Barnali; Sofack-Kreutzer, Julien; Ghani, Amylia Abdul; D'Elia, Valerio; Pelletier, Jeremie; Cokoja, Mirza; Kühn, Fritz; Basset, Jean-Marie
Publisher(s):
Royal Society of Chemistry (RSC); Royal Society of Chemistry; The Royal Society of Chemistry
Tags:
Chemical Engineering
article description
Homoleptic Nb-complexes combined with selected organic nucleophiles generate very active catalytic systems for the cycloaddition of propylene oxide and CO under ambient conditions. An unprecedented reaction pathway towards an acyclic organic carbonate is observed when extending the study to [Nb(OEt)] 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. This journal is © the Partner Organisations 2014.