An analytic expression for the rotational dephasing of an ensemble of symmetric top molecules excited by a short laser pulse is developed. This expression can be used to discern rotation from electronic and vibrational dynamics in polarization resolved studies and is computationally less demanding than numeric simulations used previously. The result agrees well with quantum mechanical treatment, both at room temperature and at cold rotational temperatures found in molecular beams. Applications to transient anisotropy and photoelectron angular distributions are given. Finally, we raise the possibility of combining transient anisotropy techniques with time-resolved photoelectron spectroscopy. \ua9 2011 Elsevier B.V. All rights reserved.Peer r...
Author Institution: Department of Chemistry, Yale University; Department of Chemistry and Rice Quant...
In general, molecules in the gas phase are free to rotate, and measurements made on such samples are...
For the purpose of desymmetrizing classical, computed profiles, we use the Egelstaff time transforma...
A semi-classical model for transient anisotropy in degenerate excited states is developed on the bas...
Rotational dynamics of quantum state selected and unselected CH3I molecules in intense femtosecond l...
We describe the implementation of a gauge-origin independent, time-dependent linear-response formali...
The main goal of this work is the detection of the directionality of molecular rotation and the char...
New dynamical applications of quantum beat spectroscopy (QBS) to molecular dynamics are employed to ...
The dynamics of a molecule subject to a short laser pulse is investigated, with focus on the averagi...
We present a method to create nondispersing rotational quantum states in an ensemble of linear molec...
The molecular dynamics of polar diatomic molecule, interacting with linearly and circularly polarise...
We provide a unified theoretical framework for recently emerging experiments that retrieve fixed-in-...
In this and the accompanying paper we present a theoretical treatment and experimental study, respec...
The photoelectron signal of the singly deprotonated fluorescein anion is found to be highly dependen...
The equations of motion for the molecular rotation are derived for vibrationally cold dimers that ar...
Author Institution: Department of Chemistry, Yale University; Department of Chemistry and Rice Quant...
In general, molecules in the gas phase are free to rotate, and measurements made on such samples are...
For the purpose of desymmetrizing classical, computed profiles, we use the Egelstaff time transforma...
A semi-classical model for transient anisotropy in degenerate excited states is developed on the bas...
Rotational dynamics of quantum state selected and unselected CH3I molecules in intense femtosecond l...
We describe the implementation of a gauge-origin independent, time-dependent linear-response formali...
The main goal of this work is the detection of the directionality of molecular rotation and the char...
New dynamical applications of quantum beat spectroscopy (QBS) to molecular dynamics are employed to ...
The dynamics of a molecule subject to a short laser pulse is investigated, with focus on the averagi...
We present a method to create nondispersing rotational quantum states in an ensemble of linear molec...
The molecular dynamics of polar diatomic molecule, interacting with linearly and circularly polarise...
We provide a unified theoretical framework for recently emerging experiments that retrieve fixed-in-...
In this and the accompanying paper we present a theoretical treatment and experimental study, respec...
The photoelectron signal of the singly deprotonated fluorescein anion is found to be highly dependen...
The equations of motion for the molecular rotation are derived for vibrationally cold dimers that ar...
Author Institution: Department of Chemistry, Yale University; Department of Chemistry and Rice Quant...
In general, molecules in the gas phase are free to rotate, and measurements made on such samples are...
For the purpose of desymmetrizing classical, computed profiles, we use the Egelstaff time transforma...