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Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene
Chemical Communications ( IF 4.9 ) Pub Date : 2024-05-08 , DOI: 10.1039/d4cc00922c
Wenhao Chen 1 , Haisheng Hu 1 , Jie Feng 1 , Lei Zhu 2 , Di Wu 1
Affiliation  

The salt metathesis of a boryl-ethynyl lithium salt {[(HCDipN)2]B-CC-Li} with a monochlorosilylene [LSi(:)Cl; L = PhC(NtBu)2] produced an isolable boryl-ethynyl silylene {1; [(HCDipN)2]B–C[triple bond, length as m-dash]C–Si(L)}. The Si(II) center in 1 possesses a nonbonding lone pair and forms a covalent bond with the ethynyl group. The characterization of 1 was carried out by multinuclear NMR spectroscopy, single-crystal X-ray structure analysis and DFT calculations. Additionally, a reactivity study of 1 was conducted towards oxygen-containing and aryl C–F substrates.

中文翻译:


硼基乙炔基硅烯的合成、结构和反应性研究



硼基-乙炔基锂盐{[(HCDipN) 2 ]B-CC-Li}与一氯亚甲硅基[LSi(:)Cl的盐复分解; L = PhC(N t Bu) 2 ] 产生可分离的硼基-乙炔基亚甲硅基 {1; [(HCDipN) 2 ]B–C [triple bond, length as m-dash] C–Si(L)}。 1中的Si(II)中心具有非键合孤对电子,并与乙炔基形成共价键。通过多核NMR谱、单晶X射线结构分析和DFT计算对1进行了表征。此外,还对含氧和芳基 C-F 底物进行了 1 的反应性研究。
更新日期:2024-05-08
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