闪光光解
光化学
量子产额
猝灭(荧光)
化学
三重态
单线态氧
乙腈
纳秒
超快激光光谱学
吸收(声学)
单重态
磷光
吸收光谱法
激发态
氧气
激光器
分析化学(期刊)
材料科学
荧光
分子
反应速率常数
原子物理学
光学
有机化学
动力学
物理
复合材料
量子力学
作者
Ann Cantrell,David J. McGarvey,Louise Mulroy,T. George Truscott
标识
DOI:10.1111/j.1751-1097.1999.tb08138.x
摘要
Abstract The results of a nanosecond laser flash photolysis investigation of the UVA sunscreen Mexoryl* SX in various solvent environments and within a commercial sunscreen formulation are reported. To the best of our knowledge this is the first laser flash photolysis study of a commercial suncare formulation. In each of these environments kinetic UV‐visible absorption measurements following nanosecond 355 nm laser excitation reveals a short‐lived species with a solvent‐dependent absorption maximum around 470–500 nm and a solvent‐dependent lifetime of ?50–120 ns. This transient absorption is attributed to the triplet state of Mexoryl* SX on the basis that it is quenched by molecular oxygen leading to the formation of singlet oxygen in acetonitrile. The singlet oxygen quantum yield (φ Δ ), determined by comparative time‐resolved near‐infrared luminescence measurements and extrapolated to the limit of complete triplet state quenching, is estimated as 0.09 ± 0.03 in acetonitrile. In aqueous solution the shorter triplet state lifetime combined with lower ambient oxygen concentrations precludes significant triplet state quenching. For the commercial sunscreen formulation there was no observable difference in the measured triplet lifetime between samples exposed to oxygen or argon, suggesting that the singlet oxygen quantum yield in such environments is likely to be orders of magnitude lower than that measured in acetonitrile.
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