We demonstrate that a helical water can be constructed and mediate inverse chirality transfer by rationally designing l-phenylalanine derivative (LPPF) featuring a geometrically matched carboxyl pocket for water. Our findings provide deeper insight into the complexity of chirality transfer by revealing a water-helicity-modulated inverse transfer mechanism.
We report a heterochiral solvent–solutematching strategy for enhancing the piezoelectricity of supramolecular nanostructures assembled from enantiomeric phenylalanine derivatives.
Conventional supramolecular co-assembly typically necessitates stoichiometric or excess guest loading to achieve effective chirality transfer, a requirement that often compromises structural fidelity and chiroptical efficiency due to inefficient stereochemical communication.
Supramolecular chiral nanocarriers successfully immobilize GOx and realize overall conformational optimization of GOx via enhanced stereoselective binding, efficiently improving GOx catalytic activity as well as tumor therapeutic efficiency.
Achieving a continuous range of helical pitches, remains a formidable challenge, as conventional methods typically rely on complex multicomponent systems that suffer from chemical heterogeneity and limited predictability.
Address: 800 Dongchuan Rd. Minhang District, Shanghai, China Tel: +86 21 54747651
Copyright © 2025 Shanghai Jiao Tong University