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Ultrafast Spectroscopy and Dynamics of Photoredox Catalysis

Journal Article · · Annual Review of Physical Chemistry
 [1];  [2];  [3];  [2]
  1. Princeton University, NJ (United States); Princeton University
  2. Florida State University, Tallahassee, FL (United States)
  3. Princeton University, NJ (United States)

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. Furthermore, 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.

Research Organization:
Princeton University, NJ (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0019370
OSTI ID:
2515565
Journal Information:
Annual Review of Physical Chemistry, Journal Name: Annual Review of Physical Chemistry Vol. 76; ISSN 0066-426X
Publisher:
Annual ReviewsCopyright Statement
Country of Publication:
United States
Language:
English

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