Transition-state theory allows for the characterization of kinetic processes in terms of enthalpy and entropy of activation by using the Eyring equation. However, for reactions in solution, it fails to take the change of viscosity of solvents with temperature into account. A second-generation unidirectional rotary molecular motor was used as a probe to study the effects of temperature-dependent viscosity changes upon unimolecular thermal isomerization processes. By combining the free-volume model with transition-state theory, a modified version of the Eyring equation was derived, in which the rate is expressed in terms of both temperature and viscosity.</p
This work was supported by the Engineering and Physical Sciences Research Council (EPSRC) [grant num...
Molecular isomerization kinetics in liquid solvents are determined by a complex interplay between th...
As molecular machines move to exciting applications in various environments, the study of medium eff...
Transition-state theory allows for the characterization of kinetic processes in terms of enthalpy an...
A detailed investigation of viscosity dependence of the isomerization rate is carried out for contin...
A detailed investigation of viscosity dependence of the isomerization rate is carried out for contin...
Abstract: In combination with viscous liquids, high pressure was effectively used to study dynamic s...
Chemical reactions almost always proceed more rapidly when the reagents are heated, and the rate usu...
Advances in the understanding of the dependence of reaction rates from temperature, as motivated fro...
Viscosity of dilute solutions of mono and dimethyl ether of polyethylene glycol in n-propanol and n-...
The modern transition state theory of reaction rates (Glasstone, Iaidler and Eyring, 1941) considers...
This note is aimed at ascertaining whether rates of Diels-Alder reactions depend on the viscosity of...
Many important chemical and biological reactions do not face a sizable activation barrier in their m...
The viscoelastic behavior of sheared fluids is calculated by Non-Equilibrium Molecular Dynamics (NEM...
Many important chemical and biological reactions do not face a sizable activation barrier in their m...
This work was supported by the Engineering and Physical Sciences Research Council (EPSRC) [grant num...
Molecular isomerization kinetics in liquid solvents are determined by a complex interplay between th...
As molecular machines move to exciting applications in various environments, the study of medium eff...
Transition-state theory allows for the characterization of kinetic processes in terms of enthalpy an...
A detailed investigation of viscosity dependence of the isomerization rate is carried out for contin...
A detailed investigation of viscosity dependence of the isomerization rate is carried out for contin...
Abstract: In combination with viscous liquids, high pressure was effectively used to study dynamic s...
Chemical reactions almost always proceed more rapidly when the reagents are heated, and the rate usu...
Advances in the understanding of the dependence of reaction rates from temperature, as motivated fro...
Viscosity of dilute solutions of mono and dimethyl ether of polyethylene glycol in n-propanol and n-...
The modern transition state theory of reaction rates (Glasstone, Iaidler and Eyring, 1941) considers...
This note is aimed at ascertaining whether rates of Diels-Alder reactions depend on the viscosity of...
Many important chemical and biological reactions do not face a sizable activation barrier in their m...
The viscoelastic behavior of sheared fluids is calculated by Non-Equilibrium Molecular Dynamics (NEM...
Many important chemical and biological reactions do not face a sizable activation barrier in their m...
This work was supported by the Engineering and Physical Sciences Research Council (EPSRC) [grant num...
Molecular isomerization kinetics in liquid solvents are determined by a complex interplay between th...
As molecular machines move to exciting applications in various environments, the study of medium eff...