化学
异氰
反应性(心理学)
稀土
环加成
晶体结构
金属
结晶学
立体化学
戒指(化学)
药物化学
催化作用
有机化学
矿物学
病理
替代医学
医学
作者
Zhengqi Chai,Junnian Wei,Wen‐Xiong Zhang
出处
期刊:Organometallics
[American Chemical Society]
日期:2023-09-06
卷期号:42 (19): 2736-2741
被引量:3
标识
DOI:10.1021/acs.organomet.3c00301
摘要
As the key intermediates in metal-catalyzed [2 + 2 + 2] cycloaddition reactions of three alkynes, main-group and transition-metal metallacycloheptatrienes have been studied for decades, but rare-earth analogues have remained illusive. Herein, we report the well-defined rare-earth metallacycloheptatrienes 2-Sc and 2-Lu obtained in high yields via the reaction of Cp*Li (Cp* = pentamethylcyclopentadienyl) and RECl3 (RE = Sc, Lu) with TMEDA-coordinated 2,2′-dilithio-Z-stilbene 1. The single-crystal structure of 2-Sc (RE = Sc) reveals it to be a separate ion pair, and the scandacycloheptatriene ring adopts a nonplanar boat-like conformation. The reactivity of compounds 2-Sc and 2-Lu has been investigated. When 2-Sc was treated with 2,6-dimethylphenyl isocyanide, compound 3 was obtained via the successive 1,1-insertion and 1,2-insertion of the isocyanide. The structure of 3 was also fully characterized.
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