Circularly polarized light (CPL) is an inherently chiral entity and is considered one of the possible deterministic signals that led to the evolution of homochirality. While accumulating examples indicate that chirality beyond the molecular level can be induced by CPL, not much is yet known about circumstances where the spin angular momentum of light competes with existing molecular chiral information during the chirality induction and amplification processes. Here we present a light-triggered supramolecular polymerization system where chiral information can both be transmitted and nonlinearly amplified in a “sergeants-and-soldiers” manner. While matching handedness with CPL resulted in further amplification, we determined that opposite handedness could override molecular information at the supramolecular level when the enantiomeric excess was low. The presence of a critical chiral bias suggests a bifurcation point in the homochirality evolution under random external chiral perturbation. Our results also highlight opportunities for the orthogonal control of supramolecular chirality decoupled from molecular chirality preexisting in the system.

Introduction of asymmetry into a supramolecular system via external chiral stimuli can contribute to the understanding of the intriguing homochirality found in nature. Circularly polarized light (CPL) is regarded as a chiral physical force with right- or left-handedness. It can induce and modulate supramolecular chirality due to preferential interaction with one enantiomer. Herein, this review focuses on the photon-to-matter chirality transfer mechanisms at the supramolecular level. Thus, asymmetric photochemical reactions are reviewed, and the creation of a chiral bias upon CPL irradiation is discussed. Furthermore, the possible mechanisms for the amplification and propagation of the bias into the supramolecular level are outlined based on the nature of the photochromic building block. Representative examples, including azobenzene derivatives, polydiacetylene, bicyclic ketone, polyfluorenes, Cn-symmetric molecules, and inorganic nanomaterials, are presented.

Few studies aiming to develop a glue with an underwater reusable adhesive property have been reported because combining the two properties of reusable adhesion and underwater adhesion into a single glue formulation is a challenging issue. Herein, preparation of a simple mixture of poly(vinyl alcohol) (PVA) and a well-known phenolic compound, namely, tannic acid (TA), results in an underwater glue exhibiting reusable adhesion. We named the adhesive VATA (PVA + TA). Using VATA, two stainless steel objects (0.77 kg each) are able to be instantly attached. In addition to the high adhesive strength, surface-applied VATA in water retains its adhesive capability even after 24 h. In contrast, cyanoacrylate applied under the same water condition rapidly loses its adhesive power. Another advantage is that VATA’s adhesion is reusable. Bonded objects can be forcibly detached, and then the detached ones can be reattached by the residual VATA. VATA maintains nearly 100% of its initial adhesive force, even after 10 repetitions of attach–detach cycles. VATA bonds various materials ranging from metals and polymers to ceramics. Particularly, we first attempt to test the toxicity of the underwater adhesives using an invertebrate nematode, Caenorhabditis elegans and gold fish (vertebrate) due to potential release to the environment.

We report the synthesis of a series of statistical terpolymer poly[(methyl methacrylate)-co-lauryl methacrylate-co-2-((3,5-bis(4-carbamoyl-3-(trifluoromethyl)phenoxy)benzyloxy)carbonylamino)ethyl methacrylate] (P(MMA-co-LMA-co-BMA)) by reversible addition–fragmentation chain transfer polymerization and their aggregation behaviors in solution. In toluene, the solution behavior of terpolymer was controlled by the molar fractions of lauryl methacrylate (LMA) and benzamide-containing methacrylate (BMA) in the polymer, which increased solubility and promoted hydrogen bonding between the primary aromatic amides, respectively. Temperature-dependent 1H NMR spectroscopy also indicated gradual dissociation of the hydrogen bonds with increasing temperature. For the polymer containing 2.7 mol % of LMA and 2.7 mol % of BMA repeating units, we demonstrated that dissolving the polymer in tetrahydrofuran as a good solvent and switching the solvent with toluene produced polymer nanoparticles with diameters of several tens of nanometers, as observed by dynamic light scattering. Intramolecular hydrogen bonding was dominant and induced the noncovalent chain collapse. When the temperature of the particle dispersion in toluene at a concentration > 30 mg/mL was increased from RT to 50 °C, a significant increase in viscosity was observed. This behavior was not observed in a toluene solution of poly(methyl methacrylate), which showed decreased viscosity at a higher temperature. The viscosity increase was accompanied by a decrease in the particle size, and both were attributed to the dissociation of some intramolecular hydrogen bonds within the particles, which can increase the number of individual chains in toluene and result in more intermolecular interactions.

Evolution of supramolecular chirality from self-assembly of achiral compounds and control over its handedness is closely related to the evolution of life and development of supramolecular materials with desired handedness. Here we report a system where the entire process of induction, control and locking of supramolecular chirality can be manipulated by light. Combination of triphenylamine and diacetylene moieties in the molecular structure allows photoinduced self-assembly of the molecule into helical aggregates in a chlorinated solvent by visible light and covalent fixation of the aggregate via photopolymerization by ultraviolet light, respectively. By using visible circularly polarized light, the supramolecular chirality of the resulting aggregates is selectively and reversibly controlled by its rotational direction, and the desired supramolecular chirality can be arrested by irradiation with ultraviolet circularly polarized light. This methodology opens a route to ward the formation of supramolecular chiral conducting nanostructures from the self-assembly of achiral molecules.