In this short review, we attempt to unfold various aspects of excited-state intramolecular
proton transfer (ESIPT) from the studies that are available up to date. Since Weller's …

J1 is deduced from an abrupt decrease in fluorescence lifetimes above this energy. The
rotamer II cannot undergo excited state tautomerization. Its electronic origin is at 311.52 nm …

Energetics of the ground and excited state intramolecular proton transfer in salicylic acid
have been studied by ab initio molecular orbital calculations using the 6-31G** basis set at …

The influence of methyl and methoxy substitution in the para position of the phenolic OH
functional group on the intramolecular proton-transfer properties of electronically excited …

Sodium salicylate (NaSA) molecule exists as salicylate anion in acetonitrile (ACN) and water
solvents, and exhibits large Stokes shifted fluorescence due to excited state intramolecular …

Infrared spectra of the OH stretching vibrations of the jet-cooled salicylic acid (SA) monomer
and dimer were measured for both their electronic ground (S0) and first excited (S1) states …

The present work examines the behavior of salicylic acid (SAL)-loaded F127 micelles as
drug nanocarriers for controlled release by means of interaction with 2, 6-dimethyl-β …

Spectral and photophysical properties of 3-hydroxy-2-naphthoic acid (3HNA) have been
investigated experimentally and theoretically. In addition to its normal fluorescence, 3HNA …

The spectral and photophysical properties of salicylic acid in various solvents have been
studied by steady state and time resolved experiments. Various emitting species have been …

The photophysics of salicylic acid (SA) monomer and dimer has been studied by using
steady-state and time-resolved spectroscopic techniques. Dilute solution in alkanes emits at …