Organometallics, volume 39, issue 9, pages 1573-1579
Ancillary Ligand and Base Influences on Nickel-Catalyzed Coupling of CO2 and Ethylene to Acrylate
Katherine B Uttley
1
,
Kenichi Shimmei
2
,
Wesley H Bernskoetter
1
1
2
Sekisui Chemical Co. Ltd., Osaka, Japan
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Publication type: Journal Article
Publication date: 2020-01-14
Journal:
Organometallics
scimago Q1
SJR: 0.654
CiteScore: 5.6
Impact factor: 2.5
ISSN: 02767333, 15206041
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
The coupling of CO2 and ethylene to produce acrylates has been an area of increasing interest in recent years following a number of studies which have empirically improved catalytic turnover. Notably, the incorporation of moderately Bronsted and Lewis basic sodium phenoxide salts, as well as zinc dust, and Lewis acidic lithium salts were found to facilitate acrylate formation in batch catalysis. Despite these advances, there has been limited investigation into the effect of the catalyst ancillary ligand and phenoxide base structure on catalytic performance. Here, a collection of 1,2-bis(dialkylphosphino)benzene and related diphosphine ligands were used to show that the influence of steric environs has a marked effect on turnover. Ancillary diphosphine ligands featuring at least two smaller alkyl substituents are needed for strong activity, while the oft-used benzene annulation of the diphosphine does not appear to be determinant in achieving high turnover values. Additionally, the investigation of a colle...
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