Telomerisation of long-chain dienes with alcohols using Pd(IMes)(dvds) catalyst

Torrente-Murciano, L., Lapkin, A., Nielsen, David J., Fallis, Ian Andrew ORCID: https://orcid.org/0000-0001-7361-0182 and Cavell, Kingsley John 2010. Telomerisation of long-chain dienes with alcohols using Pd(IMes)(dvds) catalyst. Green Chemistry 12 (5) , pp. 866-869. 10.1039/B921573E

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Abstract

Several homogeneous palladium catalysts based on PPh3 and nucleophilic carbene (NHC) ligands were screened in the telomerisation reaction of 1,3-pentadiene with methanol. A Pd(acac)2-3PPh3 system showed the highest activity; initially, poor activity was observed using the Pd(0)-NHC catalysts. However, when methanol solvent/nucleophile was replaced by longer chain alcohols 1-propanol and 1-butanol, improved activity and selectivity was observed. Similarly, 1,3-hexadiene was telomerised with 1-propanol and 1-butanol with good selectivity using Pd(IMes)(dvds) as the catalyst. Pd(II)-PPh3 systems were ineffective as catalysts for the telomerisation of 1,3-hexadiene.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry Cardiff Catalysis Institute (CCI)
Subjects:	Q Science > QD Chemistry
Publisher:	Royal Society of Chemistry
ISSN:	1463-9262
Last Modified:	18 Oct 2022 13:11
URI:	https://orca.cardiff.ac.uk/id/eprint/12850

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