Organic Two-Photon-Absorbing Photosensitizers Can Overcome Competing Light Absorption in Organic Photocatalysis

被引:0
|
作者
Kundu, Bidyut Kumar [1 ]
Bashar, Noorul [1 ]
Srivastava, Prasenjit [2 ]
Elles, Christopher G. [2 ]
Sun, Yujie [1 ]
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 43221 USA
[2] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
基金
美国国家科学基金会;
关键词
Organic photocatalysis; Two-photon absorption; Competing light absorption; Deep red light irradiation; PHOTOREDOX CATALYSIS; TRANSITION-METAL; INFRARED LIGHT; COMPLEXES;
D O I
10.1002/chem.202402856
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
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页数:9
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