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摘要
以苯并咪唑、对甲基苯胺和氯乙酰氯为原料合成二(1-苯并咪唑基)甲烷和2-氯-N-(p-甲苯基)乙酰胺,并采用溶剂热法制备了一种新型酰胺官能化氮杂环卡宾钯配合物[(amide-NHC) Pd2Cl4]。通过PXRD、TGA、FT-IR和SCD对其进行表征。结果表明,目标配合物属于单斜晶系、P21/c空间群。将[(amide-NHC) Pd2Cl4]配合物应用于Suzuki-Miyaura偶联反应,当催化剂摩尔分数为2%时,催化产率高达98.74%。
Abstract
Using benzimidazole, p-methylaniline and chloroacetyl chloride as starting materials, Bis(1-benzimidazolyl)methane and 2-chloro-N-(p-tolyl)acetamide are obtained, and synthesized into a novel amide-functionalized nitrogen-heterocyclic-carbene (NHC) palladium complex[(amide-NHC)Pd2Cl4] by solvothermal method.It is characterized by means of PXRD, TGA, FT-IR and SCD.The results show that the complex belongs to a monoclinic crystal system, P21/c space group.The catalytic yield reaches as high as 98.74% when[(amide-NHC)Pd2Cl4] complex is applied for the Suzuki-Miyaura coupling reaction, with a dosage of only 2%.
关键词
氮杂环卡宾
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Suzuki-Miyaura偶联反应
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催化
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钯配合物
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酰胺官能化
Key words
nitrogen heterocyclic carbene
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Suzuki-Miyaura cross-coupling reaction
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catalysis
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palladium complexes
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amide-functionalized
Author summay
韩悦(1997-),女,硕士研究生,研究方向为金属有机催化,875627339@qq.com
双核酰胺官能化NHC—钯(Ⅱ)配合物的合成及催化Suzuki-Miyaura交叉偶联反应研究[J].
现代化工, 2023, 43(9): 104-108 DOI:10.16606/j.cnki.issn0253-4320.2023.09.022