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Pathway Complexity of Kinetically Trapped Dipeptide-Based Metastable State: Supramolecular Structural Transformation

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Small (Weinheim an Der Bergstrasse, Germany)
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Kinetic control of supramolecular polymerization in naphthalimide-conjugated dipeptides allows precise material property tuning. This study demonstrates controlling nanostructure formation and stability by modulating solvent composition for targeted applications.

Keywords:
helicity inversionmetastable statepathway complexityphase transitionself‐assemblysolvent composition

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Area of Science:

  • Supramolecular chemistry
  • Materials science
  • Nanotechnology

Background:

  • Supramolecular polymerization complexity requires kinetic control for material property tuning.
  • Naphthalimide-conjugated dipeptides offer tunable self-assembly pathways.
  • Understanding nanostructure formation is key to controlling material properties.

Purpose of the Study:

  • To investigate the pathway complexity and structural transformation of a naphthalimide-conjugated dipeptide.
  • To explore kinetic control over supramolecular polymerization using a binary solvent system.
  • To modulate self-assembly and nanostructure formation by altering water percentage.

Main Methods:

  • Spectroscopic and microscopic investigations.
  • Controlled self-assembly in DMSO-water mixtures.
  • Analysis of kinetic vs. thermodynamic stability.

Main Results:

  • Self-assembly transitions from monomer to helical nanofibrils.
  • Kinetically trapped gel states achieved at lower water percentages.
  • Helicity modulation and thermoreversible chiral memory observed.

Conclusions:

  • Kinetic control is crucial for managing supramolecular polymerization pathways.
  • Water percentage in binary solvents effectively controls self-assembly kinetics and nanostructure.
  • The system exhibits tunable properties and chiral memory, offering potential for advanced materials.