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Title: Comparative study of stimulated proton-transfer luminescence of three chromones

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100160a010· OSTI ID:5636916
;  [1];  [2]
  1. Florida State Univ., Tallahassee (United States)
  2. Naval Research Lab., Washington, DC (United States)

The contrasting behavior of three related chromones with respect to amplified spontaneous emission (ASE) and laser action as intramolecular proton-transfer laser systems at room temperature is investigated. The intramolecular proton-transfer laser is considered a chemical laser in which the excited tautomer species is produced by a chemical reaction after photon-pumping activating a four-level laser system. The three chromones studied are 2-methyl-3-hydroxychromone, 2-phenyl-3-hydroxychromone (3-hydroxyflavone), and the natural product fisetin (3,3{prime},4{prime},7-tetrahydroxyflavone), each of which exhibits good proton-transfer fluorescences in the 500-nm region, with respective quantum yields of 0.29 (MCH), 0.36 (MCH), and 0.16 (dioxane). Low-temperature spectroscopic study and picosecond transient absorption spectroscopy reveals that fluorescence quenching from molecular aggregation and transient parasitic S{sub n}{prime} {l arrow} S{sub 1}{prime} absorption of the tautomer both contribute to nonobservability of ASE and lasing action in the 2-methyl-3-hydroxychromone, in contrast to excellent ASE/lasing characteristics of the 3-hydroxyflavone and fisetin under comparable conditions.

DOE Contract Number:
FG05-87ER60517
OSTI ID:
5636916
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 95:7; ISSN 0022-3654
Country of Publication:
United States
Language:
English