Surface Plasmon Resonance Allows to Correlate Molecular Properties with Diffusion Coefficients of Linear Chain Alcohols

Every biological and physicochemical process occurring in a fluid phase depends on the diffusion coefficient ( D ) of the species in solution. In the present work, a model to describe and fit the behaviour of as a function of structure and extensive thermodynamics parameters in binary solutions of linear chain organic molecules is developed. Supporting experimental and computational evidences for this model are obtained by measuring for a series of ‐alcohols through a novel surface plasmon resonance method and molecular dynamics simulations. This allows to propose a kind of combined analysis to explain the dependence of on various thermodynamic and structural parameters. The results suggest that for small linear systems in the range from 0 to 200 g mol −1 and under the assumption that the diffusive activation energy is a linear function of mass, is strictly dependent on the molecular shape and on the relative strength of the solute‐solvent intermolecular forces represented by a parameter named R. The newly proposed approach can be utilized to characterize and monitor progressive changes in physicochemical properties for any investigated species upon increasing the dimension of the aggregate/molecule along a certain direction.