4.6 Article

Controlled recombination rate of lophyl radicals in cationic surfactant micelles

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ELSEVIER
DOI: 10.1016/j.colsurfa.2022.128319

Keywords

Photochromism; Lophine dimer; Cationic surfactants; Micelles; Solubilization; Reaction rate

Funding

  1. JSPS KAKENHI [JP20K15248]
  2. [2019C0007]

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This study aimed to control the recombination rate of lophyl radicals in micelles formed by cationic surfactants with different alkyl chain lengths. The results showed that the recombination rate was enhanced in micellar solutions with shorter alkyl chain surfactants compared to those with longer alkyl chain surfactants. Small-angle neutron scattering measurements revealed that elliptical micelles were formed in mixtures of the surfactant and the lophine dimer derivative, with a smaller inner volume observed when shorter chain surfactants were used. Evaluation of kinetic parameters indicated a higher randomness of the lophyl radicals in the micelles with shorter surfactant chains. These findings suggest that the size of the confined space formed by the micelles plays a crucial role in determining the recombination rate of lophyl radicals.
In this study, we aimed to control the recombination rate of lophyl radicals in micelles, which were produced from a lophine dimer by ultraviolet irradiation, formed by cationic surfactants with different alkyl chain lengths. The recombination rate in the micellar solution of the surfactant with a shorter alkyl chain was enhanced compared to that with a longer alkyl chain. Small-angle neutron scattering measurements showed that mixtures of the cationic surfactant and the lophine dimer derivative formed elliptical micelles, and a smaller inner volume was observed when shorter chain surfactants were used. Furthermore, evaluation of the kinetic parameters indicated that the randomness of the lophyl radical in the shorter surfactant micelle was higher than that in the longer surfactant micelle. These results revealed that the size of the confined space formed by the micelles determines the recombination rate of the lophyl radicals. This provides a new methodology for the development of volatile and nonvolatile molecular memories with arbitrary retention times and future quantum computing based on photochromic compounds.

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