Functionalization and Hydrogenation of Carbon Chains Derived from CO

23 December 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Selective reactions that combine H2, CO and organic electrophiles (aldehyde, ketones, isocyanide) to form hydrogenated C3 and C4 carbon chains are reported. These reactions proceed by CO homologation mediated by [W(CO)6] and an aluminum(I) reductant, followed by functionalization and hydrogenation of the chain ends. A combination of kinetics (rates, KIEs) and DFT calculations has been used to gain insight into a key step which involves hydrogenation of a metallocarbene intermediate. These findings expand the extremely small scope of systems that combine H2 and CO to make well-defined products with complete control over chain length and functionality.

Keywords

CO
Fischer-Tropsch
Hydrogenation
Homologation
Metallocarbene
aluminium(I)

Supplementary materials

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Description
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Supporting Information
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Experimental procedures, data, computational
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Supplementary weblinks

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