Aggregation-enhanced emissions of intramolecular excimers in disubstituted polyacetylenes

Whereas chain aggregation commonly quenches light emission of conjugated polymers, we here report a phenomenon of aggregation-induced emission enhancement (AIEE): luminescence of polyacetylenes is dramatically boosted by aggregate formation. Upon photoexcitation, poly(1-phenyl-1-alkyne)s and poly(diphenylacetylene)s emit blue and green lights, respectively, in dilute THF solutions. The polymers become more emissive when their chains are induced to aggregate by adding water into their THF solutions. The polymer emissions are also enhanced by increasing concentration and decreasing temperature. Lifetime measurements reveal that the excited species of the polymers become longer-lived in the aggregates. Conformational simulations suggest that the polymer chains contain n=3 repeat units that facilitate the formation of intramolecular excimers. The AIEE effects of the polymers are rationalized to be caused by the restrictions of their intramolecular rotations by the aggregate formation.     

Copper(I)-mediated cascade reactions: an efficient approach to the synthesis of functionalized benzofuro[3,2-d]pyrimidines

A novel cascade reaction was developed for the synthesis of diverse members of a series of benzofuro[3,2-d]pyrimidine derivatives. The process utilizes readily prepared 3-chlorochromenones and various commercially available amidines and their analogues as starting materials. This tandem reaction is promoted by using a simple copper(I) reagent and involves a chemoselective Michael addition-heterocyclization-intramolecular cyclization sequence.     

Developing Novel Fabrication and Optimisation Strategies on Aggregation-Induced Emission Nanoprobe/Polyvinyl Alcohol Hydrogels for Bio-Applications

The current study describes a new technology, effective for readily preparing a fluorescent (FL) nanoprobe-based on hyperbranched polymer (HB) and aggregation-induced emission (AIE) fluorogen with high brightness to ultimately develop FL hydrogels. We prepared the AIE nanoprobe using a microfluidic platform to mix hyperbranched polymers (HB, generations 2, 3, and 4) with AIE (TPE-2BA) under shear stress and different rotation speeds (0–5 K RPM) and explored the FL properties of the AIE nanoprobe. Our results reveal that the use of HB generation 4 exhibits 30-times higher FL intensity compared to the AIE alone and is significantly brighter and more stable compared to those that are prepared using HB generations 3 and 2. In contrast to traditional methods, which are expensive and time-consuming and involve polymerization and post-functionalization to develop FL hyperbranched molecules, our proposed method offers a one-step method to prepare an AIE-HB nanoprobe with excellent FL characteristics. We employed the nanoprobe to fabricate fluorescent injectable bioadhesive gel and a hydrogel microchip based on polyvinyl alcohol (PVA). The addition of borax (50 mM) to the PVA + AIE nanoprobe results in the development of an injectable bioadhesive fluorescent gel with the ability to control AIEgen release for 300 min. When borax concentration increases two times (100 mM), the adhesion stress is more than two times bigger (7.1 mN/mm²) compared to that of gel alone (3.4 mN/mm²). Excellent dimensional stability and cell viability of the fluorescent microchip, along with its enhanced mechanical properties, proposes its potential applications in mechanobiology and understanding the impact of microstructure in cell studies.