Hierarchical Self-Assembly of J-Aggregated 1,2-Bis(2-(benzyloxy)benzylidene) Hydrazine@2β-Cyclodextrin into Left-Handed Superhelix and Its External Stimuli-Responsive Unwinding.

Induction of chirality to nanosized superstructures from hierarchical self-assembly of achiral monomeric units is an important area to understand the natural chiral amplification and evolution of life processes. We report herein that the complexation of salicylaldehyde azine, 1,2-bis(2-(benzyloxy)benzylidene)hydrazine (BSAZ), with β-cyclodextrin (β-CD) in aqueous solution results in the formation of a slipped J-aggregate (θ < 54.7°) that aggregates further into a left-handed superhelix through sterical constraints triggered by the hydrophobic effect. The structure of the monomeric BSAZ@2β-CD was elucidated by ultraviolet-visible (UV-vis), Fourier transform infrared spectroscopy (FT-IR), mass, powder X-ray diffraction (PXRD), and H, C, and C CP/MAS nuclear magnetic resonance (NMR) spectroscopy. The size, shape, and morphology of the self-aggregated hierarchy were evidenced by dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) studies. The system showed excellent aggregation induced circular dichroism (AICD) with a negative Cotton effect and a high fluorescence quantum yield of 0.33 at 620 nm in a poor solvent, water, because of the formation of a higher order excimer ( ≈ 46). The helical superstructure showed responsiveness under 254 nm UV light irradiation. Light irradiation slowly unwinds the supercoiled structure into a single strand, as was visualized by a SEM image taken after 15 min of continuous light irradiation. The excellent solvatochromic effect and the control over the formed hierarchical morphology show how a supramolecular approach tailored by noncovalent interactions can develop chiral superstructures from completely achiral molecular building blocks that would have a considerable practical value in chiroptics, templates, and chiral sensing.