We present a theory for the time evolution of the Stokes shift of a polar molecule in a polar solvent. The time-dependent solute-solvent interaction is calculated in a continuum model by replacing the surrounding solvent by a frequency-dependent dielectric continuum. An expression for the time dependence of the fluorescence maximum is derived. This expression can be considered a direct generalization of the well-known Ooshika-Lippert-Mataga equation to the time domain. We also present an approximate expression for the wavelength dependence of the dynamics of the Stokes shift, and find it to be consistent with recent experimental results. We have investigated the effect of polarizability of the solute molecule and found that for many molecul...
In this paper a novel approach to study the formation and relaxation of excited states in solution i...
The time-dependent fluorescence frequency shift of protein-attached probes has a much slower decay t...
The dynamics of the electrons for a molecule in solution is coupled to the dynamics of its polarizab...
We present a theory for the time evolution of the Stokes shift of a polar molecule in a polar solven...
We present theoretical analyses of two different aspects of the time dependence of the fluorescence ...
We present theoretical analyses of two different aspects of the time dependence of the fluorescence ...
We present here a study of the time dependent Stokes shift, performing quantum-mechanical calculatio...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The time-dependent solvation correlation function (the Stokes shift response function), which descri...
The time-dependent solvation correlation function (the Stokes shift response function), which descri...
A method is described for incorporating the vibronic transitions of a solute molecule in the calcula...
In this paper a novel approach to study the formation and relaxation of excited states in solution ...
In this paper a novel approach to study the formation and relaxation of excited states in solution i...
The time-dependent fluorescence frequency shift of protein-attached probes has a much slower decay t...
The dynamics of the electrons for a molecule in solution is coupled to the dynamics of its polarizab...
We present a theory for the time evolution of the Stokes shift of a polar molecule in a polar solven...
We present theoretical analyses of two different aspects of the time dependence of the fluorescence ...
We present theoretical analyses of two different aspects of the time dependence of the fluorescence ...
We present here a study of the time dependent Stokes shift, performing quantum-mechanical calculatio...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The relationship between the energy gap time correlation function (EGTCF), measured in optical lines...
The time-dependent solvation correlation function (the Stokes shift response function), which descri...
The time-dependent solvation correlation function (the Stokes shift response function), which descri...
A method is described for incorporating the vibronic transitions of a solute molecule in the calcula...
In this paper a novel approach to study the formation and relaxation of excited states in solution ...
In this paper a novel approach to study the formation and relaxation of excited states in solution i...
The time-dependent fluorescence frequency shift of protein-attached probes has a much slower decay t...
The dynamics of the electrons for a molecule in solution is coupled to the dynamics of its polarizab...