Transition state theory (TST) approximates the reactive flux in an elementary chemical reaction by the instantaneous flux passing through a hypersurface (the transition state) which completely divides the reactant and product regions of phase space. The rigorous classical evaluation of this instantaneous flux is carried out as a trace in phase space: effectively a multidimensional integral. We present an analysis of the momentum-space component of this flux integral for the case of a generalized reaction coordinate. The classic analysis of the canonical flux by Marcus [J. Chem. Phys. 41, 2624 (1964)] is refined by reducing the determinant which appears in the transition state partition function to a very simple form, facilitating the ensuin...
The following article appeared in Journal of Chemical Physics 136.22 (2012): 224510 and may be foun...
It has been shown recently that in order for real-time correlation functions obtained from centroid ...
A deep understanding of molecular reactions is a challenging task since the range of time and energy...
Different approaches to the evaluation of the momentum flux integral in classical transition state t...
Over the last years, a new geometrical perspective on transition state theory has been developed tha...
The role of the flux, or velocity, factor in variational transition-state theory (VTST) with a gener...
Transition state theory (TST) has historically been the most important and widely used theoretical a...
Recent developments in Transition State Theory brought about by dynamical systems theory are extende...
Reaction rates across time-dependent barriers are difficult to define and difficult to obtain using ...
Welsch R, Manthe U. Thermal flux based analysis of state-to-state reaction probabilities. Molecular ...
The transition state theory (TST), which is also known as theory of absolute reaction rates (ART) an...
In its usual classical form, activated‐complex theory assumes a particular expression for the kineti...
The transition state theory of chemical reactions has proven to be a formidable tool for analyzing c...
We introduce a simple method for characterizing reactive pathways in quantum systems. Flux auto-corr...
Transition state theory forms the basis of computing reaction rates in chemical and other systems. R...
The following article appeared in Journal of Chemical Physics 136.22 (2012): 224510 and may be foun...
It has been shown recently that in order for real-time correlation functions obtained from centroid ...
A deep understanding of molecular reactions is a challenging task since the range of time and energy...
Different approaches to the evaluation of the momentum flux integral in classical transition state t...
Over the last years, a new geometrical perspective on transition state theory has been developed tha...
The role of the flux, or velocity, factor in variational transition-state theory (VTST) with a gener...
Transition state theory (TST) has historically been the most important and widely used theoretical a...
Recent developments in Transition State Theory brought about by dynamical systems theory are extende...
Reaction rates across time-dependent barriers are difficult to define and difficult to obtain using ...
Welsch R, Manthe U. Thermal flux based analysis of state-to-state reaction probabilities. Molecular ...
The transition state theory (TST), which is also known as theory of absolute reaction rates (ART) an...
In its usual classical form, activated‐complex theory assumes a particular expression for the kineti...
The transition state theory of chemical reactions has proven to be a formidable tool for analyzing c...
We introduce a simple method for characterizing reactive pathways in quantum systems. Flux auto-corr...
Transition state theory forms the basis of computing reaction rates in chemical and other systems. R...
The following article appeared in Journal of Chemical Physics 136.22 (2012): 224510 and may be foun...
It has been shown recently that in order for real-time correlation functions obtained from centroid ...
A deep understanding of molecular reactions is a challenging task since the range of time and energy...