When a chemical reaction is driven by an external field, the transition state that the system must pass through as it changes from reactant to product—for example, an energy barrier—becomes timedependent. We show that for periodic forcing the rate of barrier crossing can be determined through stability analysis of the non-autonomous transition state. Specifically, strong agreement is observed between the difference in the Floquet exponents describing stability of the transition state trajectory, which defines a recrossing-free dividing surface [G. T. Craven, T. Bartsch, and R. Hernandez,“Persistence of transition state structure in chemical reactions driven by fields oscillating in time,”Phys. Rev. E 89, 040801(R) (2014)], and the rates cal...
One of the goals of researchers in the field of reaction dynamics is to develop an understanding of ...
Unimolecular rate theory for various types of reactions is implemented for any looseness of transiti...
Using the concept of resonant states, the expressions for the rate of assocn. and dissocn. are deriv...
The following article appeared in Journal of Chemical Physics 136.9 (2012): 091102 and may be found ...
Chemical reaction rates must increasingly be determined in systems that evolve under the control of ...
Reaction rates across time-dependent barriers are difficult to define and difficult to obtain using ...
It is known from simple middle school chemistry that reactants react into products during a chemical...
Classical transition state theory has been extended to address chemical reactions across barriers th...
Over the last years, a new geometrical perspective on transition state theory has been developed tha...
The accuracy of rate constants calculated using transition state theory depends crucially on the cor...
© 2005 American Institute of Physics. The electronic version of this article is the complete one and...
© 2005 American Physical Society. The electronic version of this article is the complete one and can...
International audienceTransition state theory (TST) provides a simple interpretation of many thermal...
AbstractUnimolecular rate theory for various types of reactions is implemented for any looseness of ...
The transition state theory of chemical reactions has proven to be a formidable tool for analyzing c...
One of the goals of researchers in the field of reaction dynamics is to develop an understanding of ...
Unimolecular rate theory for various types of reactions is implemented for any looseness of transiti...
Using the concept of resonant states, the expressions for the rate of assocn. and dissocn. are deriv...
The following article appeared in Journal of Chemical Physics 136.9 (2012): 091102 and may be found ...
Chemical reaction rates must increasingly be determined in systems that evolve under the control of ...
Reaction rates across time-dependent barriers are difficult to define and difficult to obtain using ...
It is known from simple middle school chemistry that reactants react into products during a chemical...
Classical transition state theory has been extended to address chemical reactions across barriers th...
Over the last years, a new geometrical perspective on transition state theory has been developed tha...
The accuracy of rate constants calculated using transition state theory depends crucially on the cor...
© 2005 American Institute of Physics. The electronic version of this article is the complete one and...
© 2005 American Physical Society. The electronic version of this article is the complete one and can...
International audienceTransition state theory (TST) provides a simple interpretation of many thermal...
AbstractUnimolecular rate theory for various types of reactions is implemented for any looseness of ...
The transition state theory of chemical reactions has proven to be a formidable tool for analyzing c...
One of the goals of researchers in the field of reaction dynamics is to develop an understanding of ...
Unimolecular rate theory for various types of reactions is implemented for any looseness of transiti...
Using the concept of resonant states, the expressions for the rate of assocn. and dissocn. are deriv...