Electrochemical Reductive N-Methylation with CO 2 Enabled by a Molecular Catalyst.

Autor: Rooney CL; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.; Energy Sciences Institute, Yale University, West Haven, Connecticut 06516, United States., Wu Y; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.; Energy Sciences Institute, Yale University, West Haven, Connecticut 06516, United States., Tao Z; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.; Energy Sciences Institute, Yale University, West Haven, Connecticut 06516, United States., Wang H; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.; Energy Sciences Institute, Yale University, West Haven, Connecticut 06516, United States.
Jazyk: angličtina
Zdroj: Journal of the American Chemical Society [J Am Chem Soc] 2021 Dec 01; Vol. 143 (47), pp. 19983-19991. Date of Electronic Publication: 2021 Nov 16.
DOI: 10.1021/jacs.1c10863
Abstrakt: The development of benign methylation reactions utilizing CO 2 as a one-carbon building block would enable a more sustainable chemical industry. Electrochemical CO 2 reduction has been extensively studied, but its application for reductive methylation reactions remains out of the scope of current electrocatalysis. Here, we report the first electrochemical reductive N-methylation reaction with CO 2 and demonstrate its compatibility with amines, hydroxylamines, and hydrazine. Catalyzed by cobalt phthalocyanine molecules supported on carbon nanotubes, the N-methylation reaction proceeds in aqueous media via the chemical condensation of an electrophilic carbon intermediate, proposed to be adsorbed or near-electrode formaldehyde formed from the four-electron reduction of CO 2 , with nucleophilic nitrogenous reactants and subsequent reduction. By comparing various amines, we discover that the nucleophilicity of the amine reactant is a descriptor for the C-N coupling efficacy. We extend the scope of the reaction to be compatible with cheap and abundant nitro-compounds by developing a cascade reduction process in which CO 2 and nitro-compounds are reduced concurrently to yield N -methylamines with high monomethylation selectivity via the overall transfer of 12 electrons and 12 protons.
Databáze: MEDLINE