Stepwise self-organization of hydrogen-bonded fibers in a minimalist glucose-pyrene system via CH–π-stabilized “iotamers”

Abstract

A kinetically controlled self-organization system was realized using the synthetically simple molecule 4,6-O-pyrenylidene glucose (Py-Glc). Unlike conventional supramolecular saccharide systems that converge into a thermodynamically stable state via strong hydrogen bonding, Py-Glc temporarily suppresses primary nucleation by forming kinetically favored CH–π-stabilized aggregates as a dormant product. These aggregates then directly transform into microfibers through hydrogen bonding. Notably, this transformation is not initiated from large aggregates but “iotamers” such as dimers, trimers, or tetramers. This stepwise transition is significantly accelerated by the addition of fibrous seeds. To the best of our knowledge, this is the first demonstration of the seeded self-assembly in a monosaccharide-based system. This study introduces a novel minimalist molecular-design strategy for the precise control over the self-assembly and provides a generalizable platform for carbohydrate–aromatic conjugate systems.

Graphical abstract: Stepwise self-organization of hydrogen-bonded fibers in a minimalist glucose-pyrene system via CH–π-stabilized “iotamers”

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Article information

Article type
Communication
Submitted
24 May 2025
Accepted
23 Jun 2025
First published
01 Jul 2025

Chem. Commun., 2025, Advance Article

Stepwise self-organization of hydrogen-bonded fibers in a minimalist glucose-pyrene system via CH–π-stabilized “iotamers”

M. Hirose, K. Tashiro, N. Tajima, F. Sugiura, S. Shimoda, Y. Kohno, Y. Tomita and K. Totani, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D5CC02945G

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