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Updated: Oct 25, 2025
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Published on: September 8, 2016
Non-Arrhenius kinetics and slowed-diffusion mechanism of molecular aggregation of a rhodamine dye on colloidal
Tímea Šimonová Baranyaiová1, Róbert Mészáros, Táňa Sebechlebská
1Department of Hydrosilicates, Institute of Inorganic Chemistry, Slovak Academy of Sciences, 845 36 Bratislava, Slovakia. timea.baranyaiova@savba.sk juraj.bujdak@savba.sk.
Abstract:
The non-covalent association is important for many fields of science, including processes in living systems. This work elucidates the mechanism of rhodamine 123 molecular aggregation in dispersions of a layered silicate and explains the mystery of the slow kinetics of this process. Chemometric analysis of thousands of spectra recorded by stopped-flow visible spectroscopy identified two parallel diffusion processes described by a two-phase exponential function. The slow and fast processes followed the super-Arrhenius kinetics and were assigned to lateral (surface) diffusion and inter-particle diffusion of dye cations, respectively. This work, supported by a large amount of data and their in-depth analysis, provides the first evidence of how these processes coexist together and provides quantitative analysis of their dependence on the reaction conditions. The implications of this work can be crucial for understanding the mechanism of the non-covalent association of adsorbed molecules in nature.
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