Conjugated microporous polymers for near-infrared photothermal control of shape change

Herein,a facile and highly efficient synthetic method to prepare organic photothermal materials with high photo-stability and outstanding photothermal performance is reported.Through direct polymerization of commercial aromatic monomers in the presence of anhydrous aluminium chloride and dichloromethane,four kinds of conjugated microporous polymers(CMPs)were obtained.Detailed structural analysis confirmed that the resultant CMPs possessed abundant micropores with an extendedπ-conjugated skeleton.Under near-infrared(NIR)light irradiation(808 nm,1.0 W cm−2),all the CMPs showed fast heating-up behavior with their maximum temperatures higher than 150℃.Moreover,the efficiency of photothermal conversion(η)of the CMPs was found to increase linearly with the increase in the number of conjugated benzene rings within the monomer.Poly-TPE from tetraphenylethylene(TPE)and Poly-TP from o-terphenyl(TP)showed highηvalues of over 47%.Poly-TPE was additionally used as a photothermal filler to remotely and spatially control the shape recovery of thermal-sensitive shape memory polymers(SMPs),while its introduction(1 wt%)had little influence on the thermal and mechanical properties of the polymer matrixes.Owing to their excellent NIR photothermal performance as well as a one-step synthetic preparation,these CMPs may be promising photothermal materials for practical applications.

Intrinsic persistent room temperature phosphorescence derived from 1H-benzo[f]indole itself as a guest

The influence of 1H-benzo[f]indole(Bd) and its derivatives on room temperature phosphorescence(RTP)has raised great concern since they were found to significantly affect RTP of the extensively studied carbazole(Cz) derivatives. However, the role of Bd itself existing in Cz-based or other doping systems was still unclear. In order to clarify its intrinsic phosphorescent property, Bd was introduced as a guest into different organic matrixes including substituted Cz derivatives and polymers. The phosphorescence located in 560–620 nm was confirmed to be derived from Bd itself, which can be detected whatever Bd was doped in the crystal or amorphous state of Cz derivatives. The suitable energy gap between Cz derivatives and Bd is the key to achieve ultralong RTP of Bd. Additionally, when doped in polymers with plenty of hydrogen bonds, RTP of Bd with lifetime over 280 ms was easily obtained. Among them, Bd@PHEMA(poly(hydroxyethyl methacrylate) exhibited superior phosphorescence, with yellow afterglow lasting for over 2.5 s. Therefore, this work demonstrated that a new organic RTP phosphor, Bd, is discovered, and ultralong RTP of Bd can be achieved not only doped in Cz derivatives but also in polymers as the hosts.