Related Experiment Video
Updated: Aug 23, 2025

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Visible Light-Driven Metal-Organic Framework-Mediated Activation and Utilization of CO2 for the Thiocarboxylation of
Sandhya Saini1,2, Debabrata Chakraborty3, E S Erakulan4
1Chemical & Material Sciences Division, CSIR-Indian Institute of Petroleum, Haridwar Road, Mohkampur, Dehradun 248005, India.
Abstract:
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 β-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 β-thioacids in almost quantitative yields.
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Cycloaddition Reactions: MO Requirements for Thermal Activation
Carbon-dioxide Fixation
Thermal and Photochemical Electrocyclic Reactions: Overview
Loss of Carboxy Group as CO2: Decarboxylation of β-Ketoacids
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents

