Polymerization Based on Modified β-Cyclodextrin Achieves Efficient Phosphorescence Energy Transfer for Anti-Counterfeiting.

Supramolecular polymerization can not only activate guest phosphorescence, but also promote phosphorescence Förster resonance energy transfer and induce effective delayed fluorescence. Herein, the solid supramolecular assemblies of ternary copolymers based on acrylamide, modified β-cyclodextrin (CD), and carbazole (CZ) are reported. After doping with polyvinyl alcohol (PVA) and dyes, a NIR luminescence supramolecular composite with a lifetime of 1.

Macrocycle γ-Cyclodextrin Confined Polymeric Chromophore Ultralong Phosphorescence Energy Transfer.

A multicolor persistent luminescence solid polymeric system based on macrocycle-confined phosphorescence energy transfer was constructed with γ-cyclodextrin (γ-CD) and poly(vinyl alcohol) modified by triphenylene derivative (TP-PVA). Attributed to the fact that macrocycles effectively suppress the aggregation of guests and form a rigid environment via coassembling with the polymer, the phosphorescence lifetime of the yielded polymeric films is prolonged from 0.22 to 5.

Two-Photon Excited Near-Infrared Phosphorescence Based on Secondary Supramolecular Confinement.

Organic phosphorescence materials have received wide attention in bioimaging for bio-low toxicity and large Stokes. Herein, a design strategy to achieve near-infrared (NIR) excitation and emission of organic room-temperature phosphorescence through two-stage confinement supramolecular assembly is presented. Via supramolecular macrocyclic confinement, the host-guest complexes exhibit phosphorescence with two-photon absorption (excitation wavelength up to 890 nm) and NIR emission (emission wavelength up to 800 nm) in aqueous solution, and further nano-confinement assembly significantly strengthens phosphorescence.

Highly Reversible Supramolecular Light Switch for NIR Phosphorescence Resonance Energy Transfer.

Although purely organic room-temperature phosphorescence (RTP) has drawn widespread attention in recent years, regulatable phosphorescence resonance energy transfer (PRET) supramolecular switch is still rare. Herein, single molecular dual-fold supramolecular light switches, which are constructed by phenylpyridinium salts modified diarylethene derivatives (DTE-Cn, n = 3, 5) and cucurbit[8]uril (CB[8]) are reported. Significantly, biaxial [3]pseudorotaxane displayed efficiently reversible RTP after binding with CB[8] and the phosphorescence quenching efficiency is calculated up to be 99%.

Supramolecular Purely Organic Room-Temperature Phosphorescence.

In recent years, purely organic room-temperature phosphorescence (RTP) has aroused wide concern and promotes the development of the supramolecular phosphorescence. Different from organic crystallization, polymerization, or matrix rigidification, supramolecular strategy mainly takes advantage of the synergy between supramolecular co-assembly and strong binding by macrocyclic host compounds (cucurbit[n]urils, cyclodextrins, etc.) to overcome deficiencies such as poor processability and water solubility and improves RTP materials' quantum efficiency and lifetime in the solid state or in an aqueous solution.

Supramolecular Pins with Ultralong Efficient Phosphorescence.

Constructing ultralong organic phosphorescent materials possessing a high quantum yield is challenging. Herein, assemblies of purely organic supramolecular pins composed of alkyl-bridged phenylpyridinium salts and cucurbit[8]uril (CB[8]) are reported. Different from "one host with two guests" and "head-to-tail" binding, the binding formation of supramolecular pins is "one host with one guest" and "head-to-head," which overcomes electrostatic repulsion and promotes intramolecular charge transfer.

A twin-axial pseudorotaxane for phosphorescence cell imaging.

A twin-axial pseudorotaxane is constructed using a phenylpyridine salt with diethanolamine (DA-PY) and cucurbit[8]uril (CB[8]), and it not only displays phosphorescence in aqueous solution but it can also be used for targeted cell-imaging.