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首页> 外文期刊>Journal of Chemical Education >Synthesis of well-defined copper N-heterocyclic carbene complexes and their use as catalysts for a 'click reaction': A multistep experiment that emphasizes the role of catalysis in green chemistry
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Synthesis of well-defined copper N-heterocyclic carbene complexes and their use as catalysts for a 'click reaction': A multistep experiment that emphasizes the role of catalysis in green chemistry

机译:定义明确的N-杂环卡宾铜配合物的合成及其在“点击反应”中的催化剂用途:强调催化在绿色化学中的作用的多步骤实验

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摘要

A multistep experiment for an advanced synthesis lab course that incorporates topics in organic-inorganic synthesis and catalysis and highlights green chemistry principles was developed. Students synthesized two N-heterocyclic carbene ligands, used them to prepare two well-defined copper(I) complexes and subsequently utilized the complexes as catalysts in the Huisgen 1-3 dipolar cycloaddition of benzyl azide and phenylacetylene. The catalytic reaction exhibits high atom economy, is performed without a solvent at room temperature, and is high yielding. Thus, students were able to practice and apply concepts of green chemistry through catalysis. In the process of preparing ligands and complexes, several techniques were utilized that were aimed at performing reactions more efficiently (microwave experiments) or performing reactions in benign solvents (H 2O). Another major component of this experiment is emphasis on technical writing through student preparation of formal communications and full paper using the formal ACS format.
机译:开发了一个高级合成实验室课程的多步骤实验,该课程将有机-无机合成和催化的主题纳入其中,并着重介绍了绿色化学原理。学生合成了两个N-杂环卡宾配体,用它们制备了两个明确定义的铜(I)配合物,随后将该配合物用作苄基叠氮化物和苯乙炔的Huisgen 1-3偶极环加成反应的催化剂。催化反应具有高原子经济性,在室温下无需溶剂即可进行,并且产率高。因此,学生能够通过催化实践和应用绿色化学的概念。在制备配体和配合物的过程中,利用了几种旨在更有效地进行反应(微波实验)或在良性溶剂(H 2O)中进行反应的技术。该实验的另一个主要组成部分是通过学生准备正式的交流和使用正式的ACS格式的全文来强调技术写作。

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