Nuclear dynamics of decaying states: A semiclassical approach

2013 ◽  
Vol 139 (7) ◽  
pp. 074111 ◽  
Author(s):  
N. Sisourat
Keyword(s):  
Semiclassical Approach ◽  
Nuclear Dynamics ◽  
Decaying States

Nuclear dynamics of decaying states: A time‐dependent formulation

1993 ◽  
Vol 98 (12) ◽  
pp. 9691-9706 ◽  
Author(s):  
L. S. Cederbaum ◽  
F. Tarantelli
Keyword(s):  
Time Dependent ◽  
Nuclear Dynamics ◽  
Decaying States

Adiabatic and nonadiabatic effects of nuclear dynamics in spectra of decaying states: Auger spectrum of HF

1996 ◽  
Vol 105 (20) ◽  
pp. 9175-9181 ◽  
Author(s):  
E. Pahl ◽  
H.‐D. Meyer ◽  
L. S. Cederbaum ◽  
D. Minelli ◽  
F. Tarantelli
Keyword(s):  
Auger Spectrum ◽  
Nuclear Dynamics ◽  
Decaying States ◽  
Nonadiabatic Effects

A GEOMETRIC APPROACH TO DISSIPATION AND ITS APPLICATION TO DISSIPATIVE NUCLEAR DYNAMICS

1984 ◽  
Vol 45 (C6) ◽  
pp. C6-87-C6-94
Author(s):  
H. Reinhardt ◽  
R. Balian ◽  
Y. Alhassid
Keyword(s):  
Geometric Approach ◽  
Nuclear Dynamics

New Approach to the Theory of Circular Dichroism

1998 ◽  
Vol 63 (8) ◽  
pp. 1187-1201 ◽  
Author(s):  
Jaroslav Zamastil ◽  
Lubomír Skála ◽  
Petr Pančoška ◽  
Oldřich Bílek
Keyword(s):  
Electromagnetic Wave ◽  
Circular Dichroism ◽  
Electromagnetic Waves ◽  
Maxwell Equations ◽  
Optically Active ◽  
Semiclassical Approach ◽  
New Approach ◽  
Isotropic Media ◽  
New Formula ◽  
Circular Dichroïsm

Using the semiclassical approach for the description of the propagation of the electromagnetic waves in optically active isotropic media we derive a new formula for the circular dichroism parameter. The theory is based on the idea of the time damped electromagnetic wave interacting with the molecules of the sample. In this theory, the Lambert-Beer law need not be taken as an empirical law, however, it follows naturally from the requirement that the electromagnetic wave obeys the Maxwell equations.

Introduction

2018 ◽  
Author(s):  
Niels Engholm Henriksen ◽  
Flemming Yssing Hansen
Keyword(s):  
Schrödinger Equation ◽  
Schrodinger Equation ◽  
Degrees Of Freedom ◽  
State Level ◽  
Boltzmann Distribution ◽  
Theoretical Description ◽  
Time Dependent ◽  
Nuclear Dynamics ◽  
Molecular Reaction ◽  
Oppenheimer Approximation

This introductory chapter considers first the relation between molecular reaction dynamics and the major branches of physical chemistry. The concept of elementary chemical reactions at the quantized state-to-state level is discussed. The theoretical description of these reactions based on the time-dependent Schrödinger equation and the Born–Oppenheimer approximation is introduced and the resulting time-dependent Schrödinger equation describing the nuclear dynamics is discussed. The chapter concludes with a brief discussion of matter at thermal equilibrium, focusing at the Boltzmann distribution. Thus, the Boltzmann distribution for vibrational, rotational, and translational degrees of freedom is discussed and illustrated.

scholarly journals Electron–Nuclear Dynamics Accompanying Proton-Coupled Electron Transfer

2021 ◽  
Vol 143 (8) ◽  
pp. 3104-3112
Author(s):  
Yusuke Yoneda ◽  
S. Jimena Mora ◽  
James Shee ◽  
Brian L. Wadsworth ◽  
Eric A. Arsenault ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Nuclear Dynamics ◽  
Proton Coupled Electron Transfer
Sign in / Sign up

Export Citation Format

Share Document