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Ultrafast Excited-State Deactivation of the Bacterial Pigment Violacein
Author(s) -
Ashley A. Beckstead,
Yuyuan Zhang,
Jonathan K. Hilmer,
Heidi J. Smith,
Emily Bermel,
Christine M. Foreman,
Bern Kohler
Publication year - 2017
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/acs.jpca.7b05769
Subject(s) - photochemistry , quantum yield , excited state , chemistry , conical intersection , fluorescence , methanol , picosecond , acetone , chromophore , solvent , ground state , analytical chemistry (journal) , chromatography , organic chemistry , laser , optics , molecule , atomic physics , physics
The photophysical properties of the natural pigment violacein extracted from an Antarctic organism adapted to high exposure levels of UV radiation were measured in a combined steady-state and time-resolved spectroscopic study for the first time. In the low-viscosity solvents methanol and acetone, violacein exhibits low fluorescence quantum yields on the order of 10 -4 , and femtosecond transient absorption measurements reveal excited-state lifetimes of 3.2 ± 0.2 and 4.5 ± 0.2 picoseconds in methanol and acetone, respectively. As solvent viscosity is increased, both the fluorescence quantum yield and excited-state lifetime of this intensely colored pigment increase dramatically and stimulated emission decays 30-fold more slowly in glycerol than in methanol at room temperature. Excited-state deactivation is suggested to occur via a molecular-rotor mechanism in which torsion about an interring bond leads to a conical intersection with the ground state.

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