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As the investigation of high efficiency thermally activated delayed fluorescence (TADF) materials become more mature, regulating the emission properties for single organic luminescence molecules has gained increasing interest recently. Herein, the donor-acceptor compounds F-AQ comprised of fluorene and anthraquinone is reported, and it exhibits a polymorphism with muti-color emission and TADF from high-level intersystem crossing (hRISC). The photodynamics and excited-state transient species were studied by femtosecond transient absorption (fs-TA) spectroscopy. As a result, an unambiguous signal of through space charge transfer (TSCT) was observed in the fs-TA spectra of the crystal with the π-π interaction between the fluorene and anthraquinone groups, whereas the other amorphous solids and crystal only show a conventional deactivation pathway of hRISC-TADF. In this study, we successfully realize the direct observation of the morphism-dependent TSCT in a crystal, which provides the observations in solid-state ultrafast excited-state dynamics and deepens the insight into the design of potential mechanochromic materials and thermochromic utilization of the polymorphism of organic luminescence molecules.
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http://dx.doi.org/10.1038/s41467-024-55569-0 | DOI Listing |
Chem Asian J
September 2025
School of Science and Engineering, Shenzhen Institute of Molecular Aggregate Science and Engineering, The Chinese University of Hong Kong, Shenzhen (CUHK-Shenzhen), Shenzhen, 518172, China.
Organic high-temperature photothermal materials (T > 100 °C) have demonstrated significant application values because of their ability to exceed the temperature limits of traditional organic photothermal materials, enabling spatiotemporally controllable long-distance heating and high-temperature conversion of laser or sunlight. In this review, we summarize the recent progress in organic high-temperature photothermal materials, mainly including organic small molecule and polymer materials. Their photothermal conversion mechanisms and the factors influencing their performance as well as their applications, including photo controlled ignition/deflagration, photothermal induced actuators, photo controlled metal processing, and concentrated sunlight energy conversion were elaborated.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing 100029, China.
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany.
Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (HO).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Material Science & Engineering, City University of Hong Kong, Kowloon, 999077, Hong Kong P.R. China.
Organic solar cells (OSCs) with p-i-n architecture usually exhibit decent efficiency due to the easily tunable energy levels of organic interfacial layers (ILs). However, their operational lifetime is limited by the morphological instability of organic ILs especially the electron-transporting layer (ETL) that shows strong self-aggregation tendency. Besides, organic ETLs are confronted with significant challenges including large batch-to-batch variations and high costs.
View Article and Find Full Text PDFOrg Lett
September 2025
College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Helicenes are circularly polarized luminescence (CPL)-active but suffer from a fundamental tradeoff between fluorescence quantum yield (Φ) and luminescence dissymmetry factor (||). Herein, we present a strategy combining lateral π-extension and helical elongation in carbazole-embedded helicenes to address this challenge. Specifically, π-extended diaza[7]helicene () and diaza[9]helicene () were synthesized and characterized, revealing nearly a 2-fold increase in Φ and a 6-fold enhancement in || from to .
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