烯类反应
桤木
己烯
1-己烯
Diels-Alder反应
化学
药物化学
有机化学
生物
植物
乙烯
催化作用
作者
Jingqin Xu,Puyi Lang,Shijie Liang,Jie Zhang,Yunfan Fei,Yajie Wang,Dexiang Gao,Takanori Hattori,Jun Abe,Xiao Dong,Haiyan Zheng,Kuo Li
标识
DOI:10.1021/acs.jpclett.4c03696
摘要
The Alder-ene reaction is a chemical reaction between an alkene with an allylic hydrogen, and it provides an efficient method to construct the C-C bond. Traditionally, this reaction requires catalysts, high temperatures, or photocatalysis. In this study, we reported a high-pressure-induced solid-state Alder-ene reaction of 1-hexene at room temperature without a catalyst. 1-Hexene crystallizes at 4.3 GPa and polymerizes at 18 GPa, forming olefins. By exploring gas chromatography-mass spectrometry, we discovered that 1-hexene generates dimeric products through the Alder-ene reaction under high pressures. The in situ neutron diffraction shows that the reaction process did not obey the topochemical rule. A six-membered ring transition state including one C-H σ bond and two alkene π bonds was evidenced by the theoretical calculation, whose energy obviously decreased when compressed to 20 GPa. Our work offers a novel and promising method to realize the Alder-ene reaction at room temperature without a catalyst, expanding the application of this important reaction.
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