Related Experiment Video
Updated: Jun 18, 2026

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
Published on: January 16, 2016
A dimensionless reaction coordinate for quantifying the lateness of transition states
1School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive N.W., Atlanta, Georgia 30332-0100, USA. thomasamanz@gmail.com
Abstract:
The Hammond-Leffler postulate asserts that transition states of exothermic reactions are reactant-like (early), whereas transition states of endothermic reactions are product-like (late). Related postulates have been proposed to describe the sensitivity of activation barriers for reactions occurring on catalytic surfaces to the catalyst structure. To evaluate the validity of these postulates for different chemical reactions, a general method for classifying transition states as either early or late is needed. One can envision a dimensionless reaction coordinate that changes continuously and monotonically from 0 to 1 along a minimum energy reaction pathway. The value of the dimensionless reaction coordinate for the transition state (W(TS)) classifies transition states as (a) early when W(TS) < 0.5, (b) late when W(TS) > 0.5, and (c) equidistant between reactants and products when W(TS) = 0.5. In this article, we derive such a dimensionless reaction coordinate and illustrate its usefulness for several different chemical reactions.
More Related Videos
Related Concept Videos
Transition State Theory
Energy Diagrams, Transition States, and Intermediates
Free Energy Changes for Nonstandard States
Reaction Quotient
Reaction Mechanisms: The Steady-State Approximation
Reaction Mechanisms: Rate-limiting Step Approximation

