Non-Arrhenius kinetics and slowed-diffusion mechanism of molecular aggregation of a rhodamine dye on colloidal particles

被引:4
作者
Simonova Baranyaiova, Timea [1 ,2 ]
Meszaros, Robert [2 ,3 ]
Sebechlebska, Tana [4 ]
Bujdak, Juraj [1 ,4 ]
机构
[1] Slovak Acad Sci, Inst Inorgan Chem, Dept Hydrosilicates, Bratislava 84536, Slovakia
[2] J Selye Univ, Dept Chem, Fac Educ, Komarno 94501, Slovakia
[3] Eotvos Lorand Univ, Inst Chem, Lab Interfaces & Nanosized Syst, H-1117 Budapest, Hungary
[4] Comenius Univ, Dept Phys & Theoret Chem, Fac Nat Sci, Bratislava 84215, Slovakia
关键词
SURFACE; ADSORPTION; TEMPERATURE; PORPHYRIN; FILMS;
D O I
10.1039/d1cp02762j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:17177 / 17185
页数:9
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