Organic Two‐Photon‐Absorbing Photosensitizers Can Overcome Competing Light Absorption in Organic Photocatalysis
Year: 2024
Type: article
Abstract: Conventional organic photocatalysis typically relies on ultraviolet and short‐wavelength visible photons as the energy source. However, this approach often suffers from competing light absorption by reactants, products, intermediates, and co‐catalysts, leading to reduced quantum efficiency and side reactions. To address this issue, we developed novel organic two‐photon‐absorbing (TPA) photosensitizers capable of functioning under deep red and near‐infrared light irradiation. Three model reactions including cyclization, Sonogashira Csp2−Csp cross‐coupling, and Csp2−N cross‐coupling reactions were selected to compare the performance of the new photosensitizers under both blue (427 nm) and deep red (660 nm) light irradiation. The obtained results unambiguously prove that for reactions involving blue light‐absorbing reactants, products, and/or co‐catalysts, deep red light source resulted in better performance than blue light when utilizing our TPA photosensitizers. This work highlights the potential of our metal‐free TPA photosensitizers as a sustainable and effective solution to mitigate the competing light absorption issue in photocatalysis, not only expanding the scope of organic photocatalysts but also reducing reliance on expensive Ru/Ir/Os‐based photosensitizers.
Source: Chemistry - A European Journal
Institutions: University of Cincinnati, University of Kansas
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,640
Awards: Broadband Two-Photon Absorption Spectroscopy for High-Repetition-Rate Lasers, G2456652341, MRI: Acquisition of an Ultrafast Transient Absorption Spectrometer, G4956514315, G5068176270, Collaborative Research: Photocatalytic Ketyl and Amino Radicals-Initiated C-C Bond Formation via Semiconductor-Based Photocatalysts, G7266148261, G8542932225
OpenAlex ID: W4402267360
