The influence of chirality on cell behavior is closely related with relevant biological events; however, many recent studies only focus on the apparent chiral influence of supramolecular nanofibers and ignore the respective effects of molecular chirality and supramolecular chirality in biological processes. Herein, the inherent molecular and supramolecular chiral effects on cell spreading and differentiation are studied. Left-handed nanofibers (referring to supramolecular chirality) assembled from L-amino acid derivatives can enhance cell spreading and proliferation compared to flat L-surfaces (referring to molecular chirality). However, compared to the D-surfaces (referring to molecular chirality), right-handed nanofibers (referring to supramolecular chirality) derived from D-amino acid suppress cell spreading and proliferation, overturning the conventional view that a fibrous morphology generally enhances cell adhesion. The results directly suggest that the amplification of chirality from chiral molecules to chiral assemblies significantly enhances the effect on regulated cell behavior by supramolecular helical handedness. Moreover, cell differentiation is found to be chirality dependent. It suggests that both the L-amino acid derivatives and the left-handed fibers facilitate osteogenic differentiation. This study provides useful insight into understanding the origin of chiral expression from the molecular to the macroscopic level in nature.

Achiral commercial aromatic molecules co-assembly with chiral phenylalanine derived gelators exhibiting strong full-color and white CPL with high glum values via chirality transfer.

Controlling the handedness of dynamic helical nanostructures of supramolecular assemblies by external stimuli is of great fundamental significance with appealing morphologydependent applications. Significantly, access to in situ chirality transformation of dynamic multistimuli-responsive systems can provide channels for real-time monitoring of the transfer processes in biological systems. However, efforts to achieve helix inversion in an all-gel-state and to comprehend the phenomena at a molecular scale are scarce. Herein, we introduce an example of supramolecular hydrogel in which graphene oxide (GO) incorporation leads to opposite helicity of the Lphenylalanine derivative (LPFEG) upon UV irradiation. The gelator modulates different degrees of packing that are responsible for the initial construction of right-handed nanofibers in GO surfaces and for the change in helix to preferred left-handedness in RGO surfaces caused by GO reduction. Specifically, LPFEG shows a mixture of right-and left-handed nanofibers with an appropriate exposure to UV light. A thermalreversible transformation of chirality is also discovered in the supramolecular assemblies, allowing a dynamic and invertible flip of helicity upon heating and cooling. The morphology transformation makes the hybrid an ideal candidate for application in a precisely controlled drug delivery process. It can unexpectedly serve as a photosensitizer and a carrier for enantioselective absorption of specific chiral drugs enantiomer (L-dopa and S-naproxen sodium) and also exhibit on-demand drug release due to the helix reversal induced by light irradiation. Our results illustrate how the surface reactivity can direct the helical organization of adsorbed fibers, which in turn provide control over enantioselective absorption of chiral drug enantiomers, further giving rise to on-demand drug release due to handedness inversion upon UV irradiation.

Having control over the supramolecular chirality through multiexternal stimulators provides many possibilities in realizing functional chiral materials. Herein, the supramolecular chirality of nanotwists comprising PA centered with 1,4-phenyldicarboxamide bearing two l/d-helicogenic alanine motifs and achiral COOH at each terminus of the alanine arms is modulated by solvent, temperature, and ultrasound. The modulations are mainly due to the hydrogen bonds among gelators and solvent-gelator interactions, resulting in changes of the molecular arrangement and subsequent self-assembled nanostructures. Typically, the gel of PA in ethyl acetate prepared by ultrasonication method exhibits thixotropic property due to the participation of ethyl acetate in the self-assembly process, resulting in relatively flexible and tolerant networks. This study provides a simplistic way to control the handedness of chiral nanostructures and a rational design of the self-assembly system with multistimuli-responsive supramolecular chirality.

The development of enantioselective recognition is of great significance in medical science and pharmaceutical industry, which associates with the molecular recognition phenomenon widely observed in biological systems. In particular, the facile and straight achievement of visual enantioselective recognition has been drawing increasing consideration, but it is still a challenge. Herein, a heterochiral diphenylalanine-based gelator (LFDF) is synthesized, presenting left-handed nanofibers during self-assembly in ethanol, which accomplishes the phenylalaninol enantiomer recognition on multiple platforms. When adding L-or D-phenylalaninol into LFDF supramolecular solution followed by ultrasonic treatment, precipitate and gel are formed, respectively. Meanwhile, LFDF supramolecular gel completely collapses in a minute after dropping L-phenylalaninol, while the gel almost remains when D-type is employed. Moreover, a fluorescent supramolecular xerogel (ThT−LFDF) is fabricated by combining the LFDF gelator with thioflavine T (ThT), which could detect L-phenylalaninol accompanying with fluorescence quenching while D-type with barely decreasing. And the ThT−LFDF xerogel system shows a good sensitivity (reaches to ppm) for the detection of Lphenylalaninol. It is found that the chirality of the assembled nanofibers, as well as amino and carboxyl of phenylalaninol, plays a critical role on the discrimination process. The multiple and visible enantioselective recognition of phenylalaninol through chiral supramolecular self-assemblies shows potential applications in the fields of medical science and pharmaceutical industry.

Recently, photoresponsive hydrogels have attracted increasing interest due to their ability to provide precise spatial and temporal control of drug release. Herein, a new kind of coumarin‐based photoresponsive supramolecular hydrogelator without conventional gelation motif is designed and synthesized through a facile one‐pot method. The gelation process, photoresponsiveness, self‐assembly morphology, self‐assembly mechanism, and release kinetics are fully investigated by various characterization methods (e.g., scanning electron microscopy, single crystal X‐ray diffraction, high pressure liquid chromatography, UV–vis spectroscopy). Furthermore, encapsulated methyl violet dye molecules can be precisely released from the hydrogel by manipulating photoirradiation time. The study reveals that the coumarin‐based photoresponsive hydrogel holds great potential as soft materials for controllable drug release.

Although chiral nanostructures have been fabricated at various structural levels, the transfer and amplification of chirality from molecules to supramolecular self‐assemblies are still puzzling, especially for heterochiral molecules. Herein, four series of C2‐symmetrical dipeptide‐based derivatives bearing various amino acid sequences and different chiralities are designed and synthesized. The transcription and amplification of molecular chirality to supramolecular assemblies are achieved. The results show that supramolecular chirality is only determined by the amino acid adjacent to the benzene core, irrespective of the absolute configuration of the C‐terminal amino acid. In addition, molecular chirality also has a significant influence on the gelation behavior. For the diphenylalanine‐based gelators, the homochiral gelators can be gelled through a conventional heating–cooling process, whereas heterochiral gelators form translucent stable gels under sonication. The racemic gels possess higher mechanical properties than those of the pure enantiomers. All of these results contribute to an increasing knowledge over control of the generation of specific chiral supramolecular structures and the development of new optimized strategies to achieve functional supramolecular organogels through heterochiral and racemic systems.

Supramolecular assemblies with diverse morphologies are crucial in determining their biochemical or physical properties. However, the topological evolution and self‐assembly intermediates as well as the mechanism remain elusive. Herein, a dynamic morphological evolution from solid nanospheres to superhelical nanofibers is revealed via self‐assembly of a minimal l‐tryptophan‐based derivative (LPWM) with various mixed solvent combinations, including the formation of solid nanospheres, the fusion of nanospheres into pearling necklace, the disintegration of necklace into short nanofibers, the distortion of nanofibers into nanotwists, and the entanglement of nanotwists into superhelices. It is found that the breakage of intramolecular H‐bonds and reconstruction of intermolecular H‐bonds, as well as the variation of aromatic interactions and hydrophobic effects, are the key driving forces for topological transformation, especially the dimensional evolution. The nanospheres and nanofibers demonstrate discrepant behaviors towards mouse neural stem cell (NSC) differentiation that compared with negligible impact of nanospheres scaffold, the nanofibers scaffold is favorable for NSC differentiation into neurons. The remarkable dynamic regulation of assembly process, together with the NSC differentiation on twisted nanofibers are making this system an ideal model to interpret complex proteins fibrillation processes and investigate the structure–function relationship.