Issue 42, 2020

Palladium-catalysed methoxycarbonylation of ethene with bidentate diphosphine ligands: a density functional theory study

Abstract

Catalytic methoxycarbonylation of ethene with a bidentate tertiary phosphine (DTBPX) and palladium has been explored at the B3PW91-D3/PCM level of density functional theory. Three different pathways for formation of methyl propanoate (MePro) have been studied, namely carbomethoxy (A), ketene (B) and hydride-hydroxyalkylpalladium pathways (C), the latter of which is favoured because it has the lowest overall kinetic barrier. After intermolecular methanolysis, a hydroxyalkylpalladium complex has been characterised on pathway C, which eventually leads to the low overall barrier to produce MePro. The possibility of copolymerisation leading to oligo-/polymers has also been considered. With a computed selectivity of >99% towards the formation of MePro and a reasonably low overall kinetic barrier of 23.0 kcal mol−1, pathway C appears to be the most plausible one. Consistent with experimental data, the overall barrier increases to 30.1 kcal mol−1 for a less bulky bidentate phosphine.

Graphical abstract: Palladium-catalysed methoxycarbonylation of ethene with bidentate diphosphine ligands: a density functional theory study

Supplementary files

Article information

Article type
Paper
Submitted
22 8 2020
Accepted
13 10 2020
First published
13 10 2020
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2020,22, 24330-24336

Palladium-catalysed methoxycarbonylation of ethene with bidentate diphosphine ligands: a density functional theory study

S. Ahmad, L. E. Crawford and M. Bühl, Phys. Chem. Chem. Phys., 2020, 22, 24330 DOI: 10.1039/D0CP04454G

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