A tunable multicolor luminescent supramolecular system was designed in aqueous media employing the self-assembly of a cationic amphiphilic cyanostilbene and the host–guest chemistry of cucurbit[7]uril.

Amphiphilic di-cationic cyanostilbene derivatives with aggregation induced emission (AIE) features formed luminescent supramolecular polymers in aqueous media. They bind bio-polyanion heparin, a known anticoagulant, in a multivalent fashion through the...

The assembly of organic dyes on bio-molecular templates is an attractive strategy for the creation of bio-materials with intriguing optical properties. This principle is exploited here for the detection of...

Photo-responsive supramolecular systems offer intriguing functional aspects which have led to their applications in diverse fields such as optoelectronics and biomedicine. However, the modulation of the luminescence output in a spatiotemporal fashion by photo-controlled transformation still remains a challenging task. Herein, we report the controlled regulation of the emission color of supramolecular assemblies of amphiphilic cyanostilbenes (CSs) in water through in situ photomodulation employing UV and sunlight. Due to their aggregation-induced emission (AIE) features, the CS chromophores in the supramolecular assemblies exhibited bright greenish-yellow emission. Photoirradiation predominantly led to the formation of a cyclized product exhibiting aggregation-caused quenching (ACQ) features and having efficient cyan-blue emission in water but severely quenched emission in the solid state. Hence, starting from a unicomponent scaffold, photomodulation provided tunable emission ranging from greenish-yellow to cyan-blue including white light in water. Furthermore, using the contrasting AIE and ACQ behavior of the components in the photoirradiated mixtures, we were able to design rewritable fluorescent inks and encryption in solid films indicating the practical utility of these systems.

Cucurbit[n]urils, the pumpkin shaped macrocyclic host molecules possessing a hydrophobic cavity and two identical carbonyl portals, have drawn a lot of attention in recent years due to their high‐affinity yet dynamic molecular recognition properties in water. The reversible and stimuli‐responsive nature of their host‐guest complexes imparts “smart” features leading to materials with intriguing optical, mechanical and morphological properties. In this review, we focus on the design of cucurbituril based luminescent materials in aqueous media as well in solid or film state. The design principles of fluorescent complexes, small assemblies as well as supramolecular polymers along with their stimuli‐responsive properties and applications in diverse areas such as optoelectronic devices, light harvesting, anti‐counterfeiting and information technology, cell imaging, etc are highlighted with selected examples from recent literature. We also discuss examples of room temperature phosphorescent materials derived from purely organic luminogens in the presence of cucurbiturils.