烯烃
溶剂
化学
光化学
电子
超短脉冲
溶剂效应
组合化学
有机化学
物理
催化作用
激光器
量子力学
光学
作者
Anna M. Doze,Youxin Fu,Mariangela Di Donato,Michiel Hilbers,Gert Luurtsema,Philip H. Elsinga,Wybren Jan Buma,Wiktor Szymański,Ben L. Feringa
出处
期刊:Chemical Science
[The Royal Society of Chemistry]
日期:2024-01-01
卷期号:15 (29): 11557-11563
摘要
The light-induced photocycloaddition of 9,10-phenanthrenequinone (PQ) with electron-rich alkenes (ERA), known as the PQ-ERA reaction, is a highly attractive photoclick reaction characterized by its operational simplicity and high biocompatibility. One essential aspect of photoclick reactions is their high rate, however the limited solubility of PQs often requires the use of a co-solvent. Evaluating the effect of different co-solvents on the PQ-ERA reaction and their influence on the reaction rate, we discovered that sulfur-containing compounds, in particular the frequently used solubilizing co-solvent DMSO, quench the triplet state of the PQ. These experimental results, supported by nanosecond-microsecond and ultrafast transient absorption data, show that even minimal amounts of DMSO result in a decreased lifetime of the reactive triplet state, essential for the photoclick reaction. Without DMSO as co-solvent, exceptionally high photoreaction quantum yields
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