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1.
Chem Commun (Camb) ; 59(94): 14036-14039, 2023 Nov 23.
Artigo em Inglês | MEDLINE | ID: mdl-37920990

RESUMO

Our recent Communication (S. R. Khan et al., Chem. Commun., 2022, 58, 2208) suggested that CO2 can be used as a potential oxidant under light irradiation without using any catalyst for the oxidation of aldehydes to acids at room temperature. The Comment based on the published literature on the catalytic oxidation of aromatic aldehydes by CO2 and thermodynamical data argued on the realism of the experimental data.

2.
ACS Appl Mater Interfaces ; 14(45): 50913-50922, 2022 Nov 16.
Artigo em Inglês | MEDLINE | ID: mdl-36326441

RESUMO

Visible light-mediated photoredox catalysis has emerged to be a fascinating approach for the activation of CO2 and its subsequent fixation into valuable chemicals utilizing renewable and inexhaustible solar energy. Although great progress has been made in CO2 photoreduction, visible light-assisted organic synthesis using CO2 as a reactive substrate is rarely explored. Herein, we report an efficient, facile, and economically viable photoredox-mediated approach for the synthesis of important ß-thioacids via carboxylation of olefins with CO2 and thiols over a porous functionalized metal-organic framework (MOF), Fe-MIL-101-NH2, as a photocatalyst under ambient conditions. This multicomponent reaction offers wide substrate scope, mild reaction conditions, easy work-up, cost-effective and reusable photocatalysts, and higher product selectivity. Computational studies suggested that CO2 interacts with the thiophenol-styrene adduct to facilitate the synthesis of ß-thioacids in almost quantitative yields.

3.
Chem Commun (Camb) ; 58(13): 2208-2211, 2022 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-35072682

RESUMO

A novel visible light-driven catalyst-free oxidation of aldehydes using CO2 both in batch and flow photoreactors to get corresponding acids along with the formation of CO in the effluent gas is described.

4.
Chem Commun (Camb) ; 57(95): 12800-12803, 2021 Nov 30.
Artigo em Inglês | MEDLINE | ID: mdl-34783333

RESUMO

The present work describes the first visible light-assisted, metal-free and organic base 1,1,3,3-tetramethyl guanidine (TMG) mediated synthesis of unsymmetrical methyl aryl/alkyl carbonates from the reaction of alcohols, methanol, and CO2 in high to excellent yields under atmospheric pressure and ambient temperature conditions.

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