| Literature DB >> 31660691 |
Javier Mateos1, Francesco Rigodanza1, Alberto Vega-Peñaloza1, Andrea Sartorel1, Mirco Natali2, Tommaso Bortolato1, Giorgio Pelosi3, Xavier Companyó1, Marcella Bonchio1, Luca Dell'Amico1.
Abstract
Twelve naphthochromenone photocatalysts (PCs) were synthesized on gram scale. They absorb across the UV/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*/PC.- (up to 1.65 V) and PC.+ /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.Entities:
Keywords: light-driven reactions; organocatalysis; photoredox catalysis; radical chemistry; synthetic methods
Year: 2019 PMID: 31660691 DOI: 10.1002/anie.201912455
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336