Transformation of Dipeptide‐Based Organogels into Chiral Crystals by Cryogenic Treatment

Controlled molecular assembly is an important approach for the synthesis of single‐component materials with diverse functions. Unlike traditional heat treatment or solvent modulation, cryogenic treatment at 77 K enabled the tunable transition of a self‐assembled diphenylalanine organogel into a hexagonal crystal. Under these conditions, the assembled molecules undergo an internal rearrangement in the solid state to form a well‐defined chiral crystal structure. Moreover, these assemblies exhibit enhanced emission. This strategy for the synthesis of single‐component supramolecular assemblies can create new functions by manipulating phase transitions.     

A 19th Century “Ideal” Oil Paint Medium: A Complex Hybrid Organic–Inorganic Gel

British 19th century painters such as J. M. W. Turner, commonly modified the properties of their paint by using gels called “gumtions”. These gels allowed them to easily tune the paint handling and drying properties. The fascinating properties of these “gumtions” were obtained by adding lead acetate to a ternary system based on mastic resin, linseed oil and turpentine. Herein, we report and investigate in depth the rheological properties of these gels as well as their structure at a molecular and supra‐molecular scale.     

Organogelator–Cellulose Composite for Practical and Eco‐Friendly Marine Oil‐Spill Recovery

Marine oil spills pose serious threats to the ecosystem and economy. There is much interest in developing sorbents that can tackle such spills. We have developed a novel sorbent by impregnating cellulose pulp with a sugar‐derived oleogelator, 1,2:5,6‐di‐O ‐cyclohexylidene‐mannitol. The gelator molecules mask the surface‐exposed hydroxyl groups of cellulose fibrils by engaging them in H‐bonding and expose their hydrophobic parts making the fibers temporarily hydrophobic (water contact angle 110°). This sorbent absorbs oil effectively, selectively and instantly from oil–water mixtures due to its hydrophobicity. Then the gelator molecules get released uniformly in the oil and later self‐assemble to fibers, as evident from SEM analysis, congealing the oil within the matrix. This hierarchical entrapment of the oil by non‐covalent polymeric fibers within a covalent polymer matrix makes the gel very strong (230‐fold increase in the yield stress) and rigid, making it suitable for practical use.     

Enhanced Circularly Polarized Luminescence in Emissive Charge‐Transfer Complexes

Achieving a large dissymmetry factor (g_lum) is a challenge in the field of circularly polarized luminescence (CPL). A chiral charge‐transfer (CT) system consisting of chiral electron donor and achiral electron acceptor shows bright circularly polarized emission with large g_lum value. The chiral emissive CT complexes could be fabricated through various approaches, such as grinding, crystallization, spin coating, and gelatinization, by simply blending chiral donor and achiral acceptor. The structural synergy originating from π–π stacking and strong CT interactions resulted in the long‐range ordered self‐assembly, enabling the formation of supramolecular gels. Benefiting from the large magnetic dipole transition moment in the CT state, the CPL activity of CT complexes exhibited large circular polarization. Our design strategy of the chiral emissive CT complexes is expected to help the development of new molecular engineering strategies for designing highly efficient CPL‐active materials.