摘要
Abundant reversible noncovalent interactions contribute greatly to the anisotropy of supramolecular morphologies and the transformation across multiple structures. However, the trigger (group) to drive the transformation remains obscure. Herein, H-bonding between free N-terminal amines of l-tryptophan derivatives (GTCn) and DMSO, triggering a morphological transition is revealed from flat to twisted nanoribbons by tuning DMSO/H2O ratios. Corresponding dynamic macroscopic morphology evolution from an aggregated cluster to a flower-like sphere of gel is observed under an optical microscope. Combined experiments and molecular dynamics (MD) simulations establish this H-bonding as the submolecular trigger, which simultaneously induces the change of π–π stacking, from the J-type to H-type. Alkyl chains at the C-terminus modulate structural dimensions, while gel thixotropy is governed by chiral morphology. These results provide a molecular strategy for precisely triggering twisted ribbon formation in self-assembly alongside the injectable chiral gel systems visible under optical microscopy.
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