光催化
发色团
超短脉冲
激发态
光谱学
光化学
化学
催化作用
纳米技术
材料科学
光催化
有机化学
物理
激光器
量子力学
光学
核物理学
作者
John Sakizadeh,Rachel Weiss,Gregory D. Scholes,Bryan Kudisch
标识
DOI:10.1146/annurev-physchem-082423-013952
摘要
Photoredox catalysis has emerged as a powerful platform for chemical synthesis, utilizing chromophore excited states as selective energy stores to surmount chemical activation barriers toward making desirable products. Developments in this field have pushed synthetic chemists to design and discover new photocatalysts with novel and impactful photoreactivity but also with uncharacterized excited states and only an approximate mechanistic understanding. This review highlights specific instances in which ultrafast spectroscopies dissected the photophysical and photochemical dynamics of new classes of photoredox catalysts and their photochemical reactions. After briefly introducing the photophysical processes and ultrafast spectroscopic methods central to this topic, the review describes selected recent examples that evoke distinct classes of photoredox catalysts with demonstrated synthetic utility and ultrafast spectroscopic characterization. This review cements the significant role of ultrafast spectroscopy in modern photocatalyzed organic transformations and institutionalizes the developing intersection of synthetic organic chemistry and physical chemistry.
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