Developing solution-processable and stable scintillators with high light yields, low detection limits and high imaging resolutions holds great significance for flexible X-ray imaging. However, attaining an optimal equilibrium among X-ray absorption capacity, exciton utilization efficiency, and decay lifetime of scintillators remains a substantial challenge. Here, a new Cu(I) halide complex was synthesized in a mild condition. It exhibits intense blue thermally activated delayed fluorescence (TADF), remarkable aggregation-induced emission (AIE) characteristic, as well as good water-oxygen stability and photochemical stability. Notably, the complex shows excellent radiation resistance and efficient radioluminescence (RL) with an ultra-low detection limit of 42.5 nGys. This superior scintillation performance can be attributed to the synergistic effect of effective X-ray absorption by the heavy CuI core, the high radiation-induced exciton utilization rate in TADF process, and the remarkable suppression of non-radiative transitions by the restriction of intramolecular motions in solid state. Furthermore, the favourable solution processability of the complex facilitates the successful fabrication of a flexible film, achieving high-quality X-ray imaging with a resolution of 17.3 lp mm. This work highlights the potential of hybrid Cu(I) halides with AIE-TADF effects for high-energy radiation detection and imaging, opening up new avenues for the exploration of cost-effective and high-performance scintillators.
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http://dx.doi.org/10.1002/anie.202422995 | DOI Listing |
J Am Chem Soc
March 2025
Department of Chemistry, University of California, Berkeley, Berkeley, California 94720, United States.
Metal halide perovskites have excellent optoelectronic properties. This study aims to determine how the optoelectronic properties of a model perovskite, cesium lead bromide (CsPbBr), change with length and thickness in one dimension (1D). By examining the photophysics of CsPbBr quantum dots (QDs), nanowires (NWs), and nanorods (NRs), we observe the influence of confinement, exciton diffusion, and trapping on their optical properties.
View Article and Find Full Text PDFOrg Lett
March 2025
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Key Laboratory of Research and Development of Natural Products, School of Pharmacy, Yunnan University, Kunming 650500, China.
Visible-light-induced transition metal (TM) catalysis has emerged as a new paradigm to discover unprecedented transformations. The reported nickel species as TM photocatalysts are mainly involved in the homolysis of Ni(II) complex or alkyl halide activation. Herein, we describe that the photoexcited nickel species could facilitate Heck cyclization by accelerating the anti-β-hydride elimination.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
March 2025
Institut für Anorganische und Analytische Chemie, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, Germany.
The complexes - (: = BuPrPSe, = Pd, = Cl; : = Bu PrPSe, = Pd, = Cl; : = Bu PrPSe, = Pd, = Br; : = Bu PrPS, = Pd, = Br; : = Bu PrPS, = Pt, = Cl) {systematic names: (-butyl-diiso-propyl-phosphine selenide-κ)di-chlorido-palladium(II), [PdCl(CHPSe)] (), (di--butyl-iso-propyl-phosphine selenide-κ)di-chloridopalladium(II), [PdCl(CHPSe)] (), di-bromido-(di--butyl-iso-propyl-phosphine selenide-κ)palladium(II), [PdBr(CHPSe)] (), di-bromido-(di--butyl-iso-propyl-phosphine sulfide-κ)palladium(II), [PdBr(CHPS)] (), di-chlorido-(di--butyl-iso-propyl-phosphine sulfide-κ)palladium(II), [PdCl(CHPS)] ()} all display a configuration with square-planar geometry at the metal atom. Compounds and are isotypic. The mol-ecules of and display crystallographic inversion symmetry; compound involves two independent mol-ecules, each with inversion symmetry but with differing orientations of the tri-alkyl-phosphane groups.
View Article and Find Full Text PDFDalton Trans
March 2025
Institute of Chemistry, University of Kassel, Heinrich-Plett-Straße 40, 34132 Kassel, Germany.
[FeCp*{N(SiMe)}] is a high-spin complex with four unpaired electrons according to SQUID magnetometry and Mößbauer spectroscopy. Its reactions with 4-dimethylaminopyridine (DMAP) and NPrX (X = Cl, Br) respectively afford [FeCp*{N(SiMe)}(DMAP)] (6), NBu[FeCp*Cl{N(SiMe)}] (7), and NPr[FeCp*Br{N(SiMe)}] (8). 7 and 8 react with formamidinium tetrafluoroborates fc[(NCHR)CH][BF] (fc = 1,1'-ferrocenylene; R = Ph, Mes) at room temperature in THF to furnish [FeCp*X{fc[(NCHR)C]}] (4: X = Cl, R = Mes; 10: X = Br, R = Mes; 11: X = Cl, R = Ph; 12: X = Br, R = Ph), which contain a ferrocene-based NHC ligand.
View Article and Find Full Text PDFDalton Trans
March 2025
Rudjer Bošković Institute, Bijenička 54, HR-10000 Zagreb, Croatia.
π-Hole interactions between a metal-bound halide and a quinoid ring are described in four novel isostructural co-crystals with the formula [Cu(terpy)ClX]·X'Q (terpy = 2,2':6',2''-terpyridine; Q = quinone; X = Br, I; X' = Cl, Br). An unusually strong π-hole interaction between Cu-X and the quinoid ring is noted. Periodic DFT computations estimate the energy of the X⋯quinone interaction to be -20.
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