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Non-digestible oligosaccharides are known to exert health-promoting effects. However, the specific mechanisms by which they regulate host physiology remain unclear. Understanding these mechanisms will facilitate the development of non-digestible oligosaccharide compositions that can achieve synergistic effects. This study selected three representative non-digestible oligosaccharides, namely xylo-oligosaccharides (XOS), galacto-oligosaccharides (GOS), and isomalto-oligosaccharides (IMO), to investigate their effects as dietary interventions on mice fed a high-fat diet. The results demonstrated that XOS and IMO synergistically mitigated weight gain and ectopic lipid deposition. Further analysis revealed that XOS significantly altered the composition of the gut microbiota, while IMO significantly enhanced insulin sensitivity via the PI3K/Akt pathway. Moreover, the combination of XOS and IMO synergistically promoted the oxidation and breakdown of fatty acids and increased the abundance of acetate and propionate-producing bacteria, such as Lactobacillus . These findings suggest a novel strategy for obesity management based on dietary intervention with XOS and IMO.

Macrocyclic thermally activated delayed fluorescence (TADF) emitters have been demonstrated to realize high efficiency OLEDs, but the design concept was still confined to rigid π-conjugated structures. In this work, two macrocyclic TADF emitters, Cy-BNFu and CyEn-BNFu, with a flexible alkyl chain as a linker and bulky aromatic hydrocarbon wrapping units were designed and synthesized. The detailed photophysical analysis demonstrates that the flexible linker significantly enhances the solution-processibility and flexibility of the parent TADF core without sacrificing the radiative transition and high PLQY. Moreover, benefiting from sufficient encapsulation of both horizontal and vertical space, the macrocyclic CyEn-BNFu further isolated the TADF core and inhibited the aggregation caused quenching, which benefits the utilization of triplet excitons. As a result, the non-doped solution-processed OLEDs based on CyEn-BNFu exhibit high maximum external quantum efficiencies (EQE) up to 32.3%, which were 3 times higher than those of the devices based on the parent molecule. In particular, these macrocyclic TADF emitters ensure the fabrication of flexible OLEDs with higher brightness, color purity and bending resistance. This work opens a way to construct macrocyclic TADF emitters with a flexible alkyl chain linker and highlights the benefits of such encapsulated macrocycles for optimizing the performance of flexible solution-processed devices., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)

The dearomative expansion of aromatic rings has long been pursued by chemists due to its potential to provide tractable approaches for synthesizing valuable non-aromatic molecules. To circumvent the conventional use of hazardous and unstable diazo compounds, photochemical synthesis has recently emerged as a promising platform. However, protocols that can effectively handle both arenes and azaarenes remain scarce. Herein, we introduce a generic strategy that efficiently converts β-(aza)aryl-β-substituted enones into biologically significant cycloheptatriene derivatives, including their aza-variants. This method allows for the easy modulation of diverse functional groups on the product and demonstrates a wide substrate scope, evidenced by its excellent tolerance to various drug motifs and good compatibility with five-membered azaarenes undergoing ring expansion. Moreover, DFT calculations of plausible mechanisms have motivated the implementation of an important cascade diradical recombination strategy for 1,3-dienones, thus facilitating the synthesis of valuable 2-oxabicyclo[3.1.0]hex-3-ene derivatives., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Developing a solution-processible blue thermally activated delayed fluorescence (TADF) emitter for hybrid white organic light emitting diodes (WOLEDs) is still a challenge. In this work, two TADF blue emitters are designed and synthesized to explore a common strategy to qualify the small molecular TADF material as a solution-processible blue host. Systematic studies find that the molecular encapsulation by introducing unconjugated carbazoles as steric shields not only keeps the intrinsic TADF feature unchanged, but also effectively suppress the intermolecular interaction induced exciton quenching, which makes the material more efficient for solution-processing. The optimized solution-processed hybrid WOLEDs based on the encapsulated TADF blue host realized a highly efficient device performance with a maximum current efficiency (CE), power efficiency (PE) and external quantum efficiency (EQE) of 45.6 cd A -1 , 40.9 lm W -1 and 17.0%, respectively, which are three times higher in device efficiency and twenty times higher in device lifetime than the corresponding device with an unencapsulated TADF blue host. Furthermore, the obtained device exhibits a high electroluminescence (EL) above 20 000 cd m -2 and a stable EL spectrum with nearly unchanged Commission International de L'Eclairage (CIE) coordinate at a wide range of applied voltages. These results clearly demonstrate that the molecular encapsulation of the TADF blue host is a superior and promising strategy to achieve high performance and color stable solution-processed hybrid WOLEDs.

The molecular aggregation and exciton-polaron interaction of the host-guest system were successfully restricted by efficient molecular encapsulation. The solution-processed blue and green TADF OLEDs have been realized with external quantum efficiencies above 23% by employing the encapsulated TADF host and guest as emission layers.

A series of carbazolone derivatives and 3-acetylindoles have been achieved via PIFA-mediated intramolecular cyclization of 2-aryl enaminones. This process allows the N-moiety on the side-chain to be annulated to the benzene ring via the metal-free oxidative aromatic C-N bond formation.