Seeking new photoresponsive materials with high energy conversion efficiency, good mechanical properties, as well as well-defined photoactuation mechanisms is of paramount significance. To address these challenges, we first introduced crystalline covalent organic frameworks (COFs) into the photoactuator field and created a facile fabrication strategy to directly install photoresponsive functional groups (i.e., acylhydrazone) on the skeletons of COFs. Herein, an approach to use polyethylene glycol (PEG) cross-linked dimers as the building blocks of the COF-42 platform was developed and afforded a series of uniform and freestanding membranes (PEG-COF-42) with outstanding mechanical properties (e.g., high flexibility and mechanical strength). Notably, these membranes possessed a fast mechanical response (e.g., bending) to UV light and good reversibility upon blue light or heating. After an in-depth investigation of the photoactuation mechanism via various techniques, we proposed a mechanism for the photoresponsive performance of PEG-COF-42: configurational change of acylhydrazone (i.e., E ↔ Z isomerization) accompanied by an excited-state intramolecular proton transfer (ESIPT) process intramolecularly transferring hydrogens from hydrogen donors (NH) to hydrogen acceptors (oxygen in PEG). Moreover, attributed to the PEG moieties, PEG-COF-42 also demonstrated a vapor-responsive performance. This study not only broadens the application scopes of COFs but also provides new opportunities for the construction of multi-stimuli-responsive materials.

A high throughput (HTP) system has been developed to exploit new functional polymers. We synthesized 25 monomers in a mini-HTP manner through the tricomponent Biginelli reaction with high yields. The starting materials were five aldehydes extracted from essential oils. The 25 corresponding polymers were conveniently prepared via mini-HTP radical polymerization initially realizing the benefit of HTP methods to quickly fabricate sample libraries. The distinct radical scavenging ability of these Biginelli polymers was evaluated through a HTP measurement to choose the three best radical scavengers. This confirms the superiority of the HTP strategy to rapidly collect and analyze data. The selected polymers have been upgraded and screened according to different requirements for biomaterials and offer water-soluble and biocompatible copolymers that effectively protect cells from the fatal UV damage. This research is a straightforward way to establish new libraries of monomers with abundant diversity. It offers polymers with interesting functionalities. This suggests that a broader study of multicomponent reactions and HTP methods might be useful in many interdisciplinary fields. To the best of our knowledge, this is the first report of a HTP study of the Biginelli reaction to develop a promising polymeric biomaterial, which might have important implications for the organic chemistry and polymer communities.

Our findings suggest arecoline promotes CD147 expression via the TGF-β1 signaling pathway in HOKs, whereas overexpression of CD147 may promote OSF progression.

No abstract