Copper(I) iodine clusters have drawn intense attention due to their advantageous photophysical properties, such as a high luminescence efficiency, large Stokes shift, and tunable luminescence lifetimes. In this work, a copper(I) iodine cluster (CuI-CHCN) was synthesized, which exhibits unique afterglow emission, ultrahigh quantum yield (90.1 % in solid state) and aggregation-induced emission (AIE) behavior. It was found that thermally activated delayed fluorescence (TADF) and long-lifetime phosphorescence occur simultaneously in CuI-CHCN. The unique photoluminescence properties of CuI-CHCN were attributed to the large spin-orbit coupling (SOC) and long-term rigidity of the crystal. The high quantum efficiency, TADF characteristics, and heavy-atom composition of CuI-CHCN endow it with excellent X-ray excited luminescence (XEL) properties, making it a promising X-ray scintillator. A flexible scintillator screen made of CuI-CHCN was successfully fabricated and used for X-ray imaging with a spatial resolution of 23.6 LP mm.
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http://dx.doi.org/10.1002/anie.202500481 | DOI Listing |
Angew Chem Int Ed Engl
February 2025
Tianjian Laboratory of Advanced Biomedical Sciences, Henan Key Laboratory of Crystalline Molecular Functional Materials, College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.
Copper(I) iodine clusters have drawn intense attention due to their advantageous photophysical properties, such as a high luminescence efficiency, large Stokes shift, and tunable luminescence lifetimes. In this work, a copper(I) iodine cluster (CuI-CHCN) was synthesized, which exhibits unique afterglow emission, ultrahigh quantum yield (90.1 % in solid state) and aggregation-induced emission (AIE) behavior.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemistry, University of Cincinnati, Cincinnati, Ohio 45221, United States.
Cu-catalyzed enantioconvergent cross-coupling of alkyl halides has emerged as a powerful strategy for synthesizing enantioenriched molecules. However, this approach is intrinsically limited by the weak reducing power of copper(I) species, which restricts the scope of compatible nucleophiles and necessitates extensive ligand optimization or the use of complex chiral scaffolds. To overcome these challenges, we introduce an aryl-radical-enabled strategy that decouples the alkyl halide activation step from the chiral Cu center.
View Article and Find Full Text PDFChemistry
December 2024
Laboratory of Analytical and Bioinorganic Chemistry, Division of Analytical and Physical Sciences, Kyoto Pharmaceutical University, 5 Nakauchi-cho, Misasagi, Yamashina-ku, Kyoto, 607-8414, Japan.
The copper-catalyzed Chan-Evans-Lam (CEL) coupling reaction advances carbon-heteroatom cross-coupling and has facilitated the development of radiohalogenation methodologies in radiochemistry. This study investigated the mechanisms and side reactions of CEL iodination under conditions relevant to radiosynthesis and typical organic synthesis, focusing on the effects of sodium iodide. The concentrations of copper and iodide, as well as the copper-to-iodide ratio, were identified as significant factors for successful copper-mediated CEL iodination, influencing the reaction mechanisms and side reactions.
View Article and Find Full Text PDFJ Am Chem Soc
June 2024
Department of Chemistry, University of Cincinnati, Cincinnati, Ohio 45221, United States.
Stepwise oxidative addition of copper(I) complexes to form copper(III) species via single electron transfer (SET) events has been widely proposed in copper catalysis. However, direct observation and detailed investigation of these fundamental steps remain elusive owing largely to the typically slow oxidative addition rate of copper(I) complexes and the instability of the copper(III) species. We report herein a novel aryl-radical-enabled stepwise oxidative addition pathway that allows for the formation of well-defined alkyl-Cu species from Cu complexes.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2023
School of Pharmacy, Third Military Medical University, Gao Tanyan Avenue, Chongqing, 400038, China.
Aryne insertions into the carbon-iodine bond of heteroaryl iodides has been achieved for the first time. This novel reaction provides an efficient pathway for the synthesis of valuable building blocks 2-iodoheterobiaryls from heteroaryl iodides and o-silylaryl triflates in excellent regioselectivity. The copper(I) catalyst, which bears a N-heterocyclic carbene (NHC) ligand, is essential to accomplish the reaction.
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