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To address and overcome the difficulties associated with the increased reactivity and susceptibility of blue emitters to deactivation pathways arising from the high-lying triplet excited states, we have successfully demonstrated an innovative strategy of harvesting triplet emission via the "thermally stimulated delayed phosphorescence" mechanism, where thermal up-conversion of excitons from the lower-energy triplet excited states (T) to higher-energy triplet excited states (T') are observed to generate blue emission. The lower-lying T excited state could serve as a mediator to populate the emissive T' state by up-conversion via reverse internal conversion, which could enhance the photoluminescence quantum yield by over 20-folds. Organic light-emitting devices with respectable external quantum efficiencies of up to 7.7% and sky-blue emission with CIE coordinates of (0.17, 0.37) have been realized. The operational stability for the device based on complex 1 has also been explored, and the device is found to show fairly respectable lifetime. This work opens up a new avenue to the design and synthesis of blue phosphorescent emitters.
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http://dx.doi.org/10.1021/jacs.8b09205 | DOI Listing |
Chemistry
September 2025
Julius-Maximilians-Universität Würzburg, Institut für Organische Chemie, Würzburg, 97074, Germany.
Photosensitization has emerged as a versatile tool to facilitate access to excited states under mild conditions, allowing for efficient and selective photochemical transformations. Herein, we report a very simple molecule, coronene bisimide (CBI), as a potent visible-light photosensitizer featuring a high extinction coefficient with a broadband absorption spanning from ultraviolet to green region of the visible spectrum, along with a long-lived triplet state generated via efficient intersystem crossing (ISC). Utilizing the triplet-triplet energy transfer (TTEnT) strategy, CBI catalyzes diverse reactions under green light irradiation.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, United States.
We report the first paramagnetic boron tetraradical, comprising four boraphenanthrene-type units with boryl radical centers bridged by a central tetraphenylethene (TPE) linker. With strongly π-accepting and sterically demanding cyclic(alkyl)(amino) carbene ligands (), spin densities localize on the boron-carbene fragments (92%), consistent with a true boron-centered tetraradical. Magnetic measurements of reveal minimal spin-spin coupling, consistent with four noninteracting = 1/2 centers.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, Yunnan 650500, China; Southwest United Graduate School, Kunming 650092, China.
Microbial-derived extracellular polymeric substances (EPS) and iron minerals are ubiquitous in aquatic environments, and they can influence the fate of organic micropollutants such as 17α-ethinylestradiol (EE2). However, the interactions between EPS and iron minerals, and their influence on EE2 photodegradation, are seldom addressed in the literature. This study explored the effects of EPS derived from different aerobic or anaerobic microbials on the reductive dissolution of ferrihydrite (Fhy) and subsequent EE2 photodegradation, with emphasis on the impact of Fe-EPS complexes formation.
View Article and Find Full Text PDFJ Phys Chem A
September 2025
School of Chemistry and Chemical Engineering, University of Southampton, Highfield, Southampton SO17 1BE, U.K.
Cyclacene carbon nanobelts are predicted to be more stable in certain vibrational states. Vibrational simulations using hybrid thermally assisted-occupation density functional theory (TAO-DFT) predict small but consistent singlet-triplet electronic excitation energy changes at the classical harmonic vibrational turning points of the smaller belts. Geometric and vibrational properties are also compared between hybrid Kohn-Sham DFT and TAO-DFT for [n]cyclacene ( = 6-14), where TAO-DFT is found to shorten the carbon-carbon bonds bridging between the two annulene ribbons and causes qualitative changes in the calculated infrared spectra.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou 515063, P. R. China.
The photophysical properties of two new Bodipy dimers are investigated using a variety of techniques, including steady-state UV-vis absorption and fluorescence spectroscopy, femtosecond and nanosecond transient absorption spectroscopy, and pulse laser-excited time-resolved electron paramagnetic resonance (TREPR) spectroscopic methods. The dimers are formed by the Bodipy units rigidly linked by the orthogonal phenylene bridge. One of the dimers is composed of iodinated units, and the other is not.
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