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作 者:刘桂杰 付正强 陈飞[1] 徐彩霞[1] 李敏[1] 刘宁[1] Liu Guijie;Fu Zhengqiang;Chen Fei;Xu Caixia;Li Min;Liu Ning(State Key Laboratory Incubation Base for Green Processing of Chemical Engineering,School of Chemistry and Chemical Engineering,Shihezi University,Shihezi,Xinjiang 832003)
机构地区:[1]石河子大学化学化工学院、化工绿色过程省部共建国家重点实验室培育基地,新疆石河子832003
出 处:《有机化学》2023年第2期629-635,共7页Chinese Journal of Organic Chemistry
基 金:Project supported by the Bingtuan Young and Middle-Aged Innovative Leading Scientists Program(No.2020CB027);the Shihezi Young and Middle-Aged Innovative Leading Scientists Program(No.2019RC01)。
摘 要:该工作发展了一类二齿N-杂环卡宾(NHC)-吡啶锰配合物催化CO_(2)和环氧化物偶联反应的方法.锰配合物和四丁基碘化铵(TBAI)构成的二元催化体系对环氧化物和CO_(2)合成环状碳酸酯的反应表现出了较高的活性.该二元催化体系适用于广泛的底物范围,例如端环氧化物和高位阻的内环氧化物.通过紫外-可见光谱、红外光谱和高分辨质谱的研究对反应机理进行了阐述.The bidentate N-heterocyclic carbene(NHC)-pyridine nitrogen manganese complex catalyzed coupling reaction of epoxides with CO_(2)was developed.The binary system resulting from the manganese complex Mn-2 in combination with tetrabutylammonium iodide(TBAI)exhibits the high activity for the synthesis of cyclic carbonate from epoxides and CO_(2).The binary catalytic system is suitable for a broad range of substrates scope,such as terminal epoxides and sterically hindered internal epoxides.A possible catalytic pathway was elaborated by UV-vis,FT-IR and HRMS method.
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