The effect of ring size on the selective carboxylation of cycloalkene oxides

Alsaiari, Raiedhah, Perrott, Luke T., Nowicka, Ewa ORCID: https://orcid.org/0000-0001-7449-2720, Engel, Rebecca V., Miedziak, Peter J., Kondrat, Simon A., Edwards, Jennifer K. ORCID: https://orcid.org/0000-0003-4089-2827, Willock, David James ORCID: https://orcid.org/0000-0002-8893-1090 and Hutchings, Graham John ORCID: https://orcid.org/0000-0001-8885-1560 2017. The effect of ring size on the selective carboxylation of cycloalkene oxides. Catalysis Science & Technology 2017 (6) , pp. 1433-1439. 10.1039/C6CY02448C

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Abstract

Carbon dioxide utilisation technology can contribute to the reduction of atmospheric CO2 levels both through its sequestration from flue gases and indirectly by relieving pressure on conventional feedstocks in chemical manufacturing. A promising approach is to employ CO2 to produce valuable cyclic carbonates (CCs) in reaction with suitable epoxides. This also has the advantage that carbon dioxide replaces toxic and hazardous reactants such as phosgene. In earlier work we have investigated the synthesis of epoxides from cycloalkenes using supported gold and gold–palladium nanoparticles as catalysts and oxygen from air as the oxidant under solvent free conditions. A strong dependence of epoxide selectivity on ring size was observed with C5 < C6 < C7 ≪ C8. In this study we extend this work to the investigation of cycloaddition of CO2 to different cycloalkene oxides with the ultimate aim of designing a process in which both epoxidation of an alkene and incorporation of CO2 could be achieved in a single process. However, we have found the opposite trend for the selectivity to carbonates: smaller ring cycloalkene oxides giving the highest carbonate selectivities while large rings do not yield CCs at all. The product distributions suggest that an alternative ring opening of the epoxides to yield alcohols and ketones is preferred under all the experimental conditions explored for larger ring systems. Additionally, the mechanism of the CC synthesis using a quaternary ammonium salt and ZnBr2 as the catalyst system was investigated using DFT methods. The results of the calculations support the experimental findings.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Advanced Research Computing @ Cardiff (ARCCA) Cardiff Catalysis Institute (CCI) Chemistry
Publisher:	Royal Society of Chemistry
ISSN:	2044-4753
Funders:	ERC, EPSRC
Date of First Compliant Deposit:	15 March 2017
Date of Acceptance:	6 March 2017
Last Modified:	07 Nov 2024 22:23
URI:	https://orca.cardiff.ac.uk/id/eprint/99009

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