Stimuli-Responsive Luminescence of an Amphiphilic Flavin Derivative via Thermodynamic and Kinetic Aggregation in Water

In this study, we investigated environmentally responsive photoluminescence color changes in water using an amphiphilic flavin derivative (1a) functionalized with an alkylsulfonate group. At low concentrations and room temperature, 1a exhibited a green emission. Upon increasing the concentration, thermodynamically stable micelle-like aggregates were formed, leading to a yellow emission. In contrast, under rapid freezing conditions, fibrous aggregates were formed under kinetic control, which also exhibited a yellow emission. These distinct aggregation modes are attributed to the cooperative effects of molecular design: the π-stacking ability of the tricyclic isoalloxazine core, flexible long alkyl chains, and the hydrophilic sulfonate moiety. This work demonstrates photoluminescent color switching based on aggregation-state control of a biogenic and potentially sustainable flavin luminophore, offering a new perspective for designing responsive and sustainable photofunctional materials.

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Publication Details

Journal
Photochem
Published
2025-09-08
DOI
https://doi.org/10.3390/photochem5030025
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Stimuli-Responsive Luminescence of an Amphiphilic Flavin Derivative via Thermodynamic and Kinetic Aggregation in Water

Soichiro Kawamorita, Takeshi Naota, Koyo Okamoto, Shufang Huang
Photochem
Luminescence and Fluorescent Materials
article

Stimuli-Responsive Luminescence of an Amphiphilic Flavin Derivative via Thermodynamic and Kinetic Aggregation in Water

Soichiro Kawamorita, Takeshi Naota, Koyo Okamoto, Shufang Huang
article en

Abstract

In this study, we investigated environmentally responsive photoluminescence color changes in water using an amphiphilic flavin derivative (1a) functionalized with an alkylsulfonate group. At low concentrations and room temperature, 1a exhibited a green emission. Upon increasing the concentration, thermodynamically stable micelle-like aggregates were formed, leading to a yellow emission. In contrast, under rapid freezing conditions, fibrous aggregates were formed under kinetic control, which also exhibited a yellow emission. These distinct aggregation modes are attributed to the cooperative effects of molecular design: the π-stacking ability of the tricyclic isoalloxazine core, flexible long alkyl chains, and the hydrophilic sulfonate moiety. This work demonstrates photoluminescent color switching based on aggregation-state control of a biogenic and potentially sustainable flavin luminophore, offering a new perspective for designing responsive and sustainable photofunctional materials.

PhotochemVol. 5(3)
Toneyama National Hospital (JP), The University of Osaka (JP)
Nihon University, Iketani Science and Technology Foundation, Toyota Physical and Chemical Research Institute, Japan Society for the Promotion of Science
Openalex Percentile: Top 81%
Luminescence and Fluorescent Materials
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