Twelve naphthochromenone photocatalysts (PCs) were synthesized on gram scale.They absorb across theUV/Vis range and feature an extremely wide redox window (up to 3.22 eV) that is accessible using simple visible light irradiation sources (CFL or LED). Their excited-state redox potentials, PC*/PCC (up to 1.65 V) and PCC+/PC* (up to 1.77 V vs. SCE), are such that these novel PCs can engage in both oxidative and reductive quenching mechanisms with strong thermodynamic requirements. The potential of these bimodal PCs was benchmarked in synthetically relevant photocatalytic processes with extreme thermodynamic requirements. Their ability to efficiently catalyze mechanistically opposite oxidative/reductive photoreactions is a unique feature of these organic photocatalysts, thus representing a decisive advance towards generality, sustainability, and cost efficiency in photocatalysis.

Naphthochromenones: Organic Bimodal Photocatalysts Engaging in Both Oxidative and Reductive Quenching Processes

MATEOS LOPEZ, JAVIER;Rigodanza F.;VEGA PENALOZA, ALBERTO;Sartorel A.;BORTOLATO, TOMMASO;Companyo X.;Bonchio M.;Dell'Amico L.
2020

Abstract

Twelve naphthochromenone photocatalysts (PCs) were synthesized on gram scale.They absorb across theUV/Vis range and feature an extremely wide redox window (up to 3.22 eV) that is accessible using simple visible light irradiation sources (CFL or LED). Their excited-state redox potentials, PC*/PCC (up to 1.65 V) and PCC+/PC* (up to 1.77 V vs. SCE), are such that these novel PCs can engage in both oxidative and reductive quenching mechanisms with strong thermodynamic requirements. The potential of these bimodal PCs was benchmarked in synthetically relevant photocatalytic processes with extreme thermodynamic requirements. Their ability to efficiently catalyze mechanistically opposite oxidative/reductive photoreactions is a unique feature of these organic photocatalysts, thus representing a decisive advance towards generality, sustainability, and cost efficiency in photocatalysis.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3318052
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