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Quenching of pH‐Responsive Luminescence of a Benzoindolizine Sensor by an Ultrafast Hydrogen Shift
Author(s) -
Zhou Jiawang,
Outlaw Victor K.,
Townsend Craig A.,
Bragg Arthur E.
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201603284
Subject(s) - chemistry , protonation , photochemistry , fluorescence , quenching (fluorescence) , stokes shift , ultrafast laser spectroscopy , tautomer , quantum yield , luminescence , absorption (acoustics) , blueshift , spectroscopy , stereochemistry , photoluminescence , materials science , ion , organic chemistry , physics , optoelectronics , quantum mechanics , composite material
Fluorescent‐sensor design requires consideration of how photochemical dynamics control properties of a sensing state. Transient absorption (TA) spectroscopy reveals an ultrafast net [1,3]‐hydrogen shift following excitation of a protonated methoxy benzoindolizine (bzi) sensor in solution. These photochemical dynamics explain a quenched pH‐responsive fluorescence shift and dramatically reduced fluorescence quantum yield relative to other (e. g. methyl) bzi compounds that do not tautomerize. Calculations predict the energetic and structural feasibility for rearrangement in protonated bzi compounds, such that interaction between the pi‐network and strongly electron‐donating methoxyl must lower the barrier for suprafacial H or H + shift across an allylic moiety. As bzi compounds broadly exhibit pH‐responsive emission shifts, chemical interactions that modulate this electronic interaction and suppress tautomerization could be used to facilitate binding‐ or surface‐specific acid‐responsive sensing.