The lithium bis(imino)stannylenoid (NIPr)2 Sn(Li)Cl (1; NIPr=bis(2,6-diisopropylphenyl)imidazolin-2-imino) was prepared by the reaction of LiNIPr with 0.5 equiv of SnCl2 ⋅diox (diox=1,4-dioxane) and the ambiphilic character of the compound was demonstrated by investigations into its reactivity. Treatment of 1 with I2 or MeI yielded the oxidative addition products (NIPr)2 SnI2 and (NIPr)2 Sn(Me)I, respectively. In contrast, the reaction of 1 with one equivalent of Me3 SiCl resulted in the formation of Me3 SiNIPr and the chlorostannylene dimer [NIPrSnCl]2 . Moreover, the substitution reaction of compound 1 with MeLi led to the formation of the methyl-substituted stannate (NIPr)2 Sn(Li)Me.
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http://dx.doi.org/10.1002/anie.201602178 | DOI Listing |
Nat Commun
November 2024
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, 610064, Chengdu, People's Republic of China.
Heavier group 14 carbene analogues, exhibiting transition-metal-like behavior, display remarkable capability for small molecule activation and coordination chemistry. However, their application in redox catalysis remains elusive. In this paper, we report the synthesis and isolation of a stannylene with carbodiphosphorane ligand.
View Article and Find Full Text PDFPrecis Chem
May 2024
Key Laboratory of Precision and Intelligent Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, China.
Metal-nitrogen double bonds have been commonly reported for conventional metal complexes, but the coexistence of both transition metal-nitrogen and lanthanide-nitrogen double bonds bridged by nitrogen within one compound has never been reported. Herein, by encapsulating a ternary transition metal-lanthanide heteronuclear dimetallic nitride into a C fullerene cage, transition metal-nitrogen and lanthanide-nitrogen double bonds are costabilized simultaneously within the as-formed clusterfullerene TiCeN@C(12)-C, which is a representative heteronuclear dimetallic nitride clusterfullerene. Its molecular structure was unambiguously determined by single-crystal X-ray diffraction, revealing a slightly bent μ-bridged nitride cluster with short Ti-N (1.
View Article and Find Full Text PDFEJNMMI Radiopharm Chem
October 2024
Department of Medical Physics, University of Wisconsin, Madison, WI, 53705, USA.
Background: Radiopharmaceutical therapy (RPT) uses radionuclides that decay via one of three therapeutically relevant decay modes (alpha, beta, and internal conversion (IC) / Auger electron (AE) emission) to deliver short range, highly damaging radiation inside of diseased cells, maintaining localized dose distribution and sparing healthy cells. Antimony-119 (Sb, t = 38.19 h, EC = 100%) is one such IC/AE emitting radionuclide, previously limited to in silico computational investigation due to barriers in production, chemical separation, and chelation.
View Article and Find Full Text PDFInorg Chem
October 2024
Key Laboratory of High-Temperature and High-Pressure Study of the Earth's Interior, Institute of Geochemistry, Chinese Academy of Sciences, Guizhou 550081, China.
Chem Commun (Camb)
October 2024
Frontiers Science Center for Flexible Electronics, Xi'an Institute of Flexible Electronics (IFE), Northwestern Polytechnical University, 127 West Youyi Road, Xi'an 710072, China.
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