Dual Photosensitizer Cycles Working Synergistically in a C(sp)-C(sp3) Cross-Coupling Reaction

被引:0
|
作者
Bryden, Megan Amy [1 ]
Villa, Marco [2 ,3 ]
Fermi, Andrea [2 ,3 ]
Ceroni, Paola [2 ,3 ]
Zysman-Colman, Eli [1 ]
机构
[1] Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Bologna, Dept Chem Ciamician, Via Selmi 2, I-40126 Bologna, Italy
[3] Univ Bologna, Ctr Chem Catalysis C3, Via Selmi 2, I-40126 Bologna, Italy
基金
英国工程与自然科学研究理事会;
关键词
TRANSITION-METAL; PHOTOREDOX;
D O I
10.1002/ajoc.202300347
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
To assess the value and reactivity of new photocatalysts (PCs), their performance should be evaluated in one or more established reactions and benchmarked against the performance using known PCs. Here, we evaluated our recently developed PC, pDTCz-DPmS, in a C(sp)-C(sp(3)) cross-coupling reaction that had been documented in the literature. Previous findings indicated this reaction could not proceed in the absence of PC; however, under our conditions this was not the case. Without PC, a moderate product yield was obtained, while this yield increased significantly upon addition of pDTCz-DPmS. UV-Vis absorption studies indicated that the Hantzsch ester (HE) additive was acting as a competitive absorber of the light from the excitation source, and quenching studies confirmed that the HE was quenched by the radical precursor, N-(acyloxy)phthalimide. Mechanistic investigations established that two parallel photosensitization pathways were in operation; a reductive quenching photocatalytic pathway (using pDTCz-DPmS) and a sacrificial photoreductant pathway (employing HE). These pathways work synergistically to enhance the yield of target product.
引用
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页数:8
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