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一种用于间歇式和连续流动式通用卡宾转移反应的完全可回收的多相铜催化剂。

A fully recyclable heterogenized Cu catalyst for the general carbene transfer reaction in batch and flow.

作者信息

Maestre Lourdes, Ozkal Erhan, Ayats Carles, Beltrán Álvaro, Díaz-Requejo M Mar, Pérez Pedro J, Pericàs Miquel A

机构信息

Laboratorio de Catálisis Homogénea , Unidad Asociada al CSIC , CIQSO-Centro de Investigación en Química Sostenible and Departamento de Química y Ciencia de Materiales , Universidad de Huelva , 21007 Huelva , Spain . Email:

Institute of Chemical Research of Catalonia (ICIQ) , Avda. Països Catalans 16 , 43007 , Tarragona , Catalonia , Spain . Email:

出版信息

Chem Sci. 2015 Feb 1;6(2):1510-1515. doi: 10.1039/c4sc03277b. Epub 2014 Nov 28.

DOI:10.1039/c4sc03277b
PMID:29560239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5811104/
Abstract

A polystyrene-linked tris(triazolyl)methanecopper(i) cationic catalyst operates under heterogeneous conditions for the reaction of ethyl diazoacetate (EDA) with an array of substrates. Carbon-hydrogen as well as X-H (X = O, N) functionalization derived from the formal transfer of the carbene moiety (:CHCOEt) from the copper center and subsequent insertion have been achieved, the reactions permitting repeated catalyst recycling and reuse. The addition of the same carbene unit to benzene leading to a cycloheptatriene derivative (Büchner reaction) or to phenylacetylene (cyclopropenation) took place at similar rates to the insertion processes and with the same catalyst recyclability. The use of this heterogenized cationic Cu catalyst in continuous flow has also been implemented. Key characteristics of the flow process are its high and constant turnover frequency (TOF) (residence times of 1 min still lead to full conversion in the reaction with ethanol after 48 h operation) and its suitability for the sequential performance of different types of carbene transfer reactions with a simple and affordable experimental setup.

摘要

一种聚苯乙烯连接的三(三唑基)甲烷铜(Ⅰ)阳离子催化剂在多相条件下用于重氮乙酸乙酯(EDA)与一系列底物的反应。通过铜中心卡宾部分(:CHCOEt)的形式转移以及随后的插入实现了碳-氢以及X-H(X = O,N)官能化,这些反应允许催化剂重复循环和再利用。相同的卡宾单元加成到苯上生成环庚三烯衍生物(布赫纳反应)或苯乙炔(环丙烷化反应)的速率与插入过程相似,并且具有相同的催化剂可循环性。这种多相化阳离子铜催化剂也已用于连续流动过程。流动过程的关键特性是其高且恒定的周转频率(TOF)(运行48小时后,停留时间为1分钟在与乙醇的反应中仍能实现完全转化)以及它适用于使用简单且经济实惠的实验装置依次进行不同类型的卡宾转移反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/c392ec5733ea/c4sc03277b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/4a6a3d35aae8/c4sc03277b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/f2fab332512e/c4sc03277b-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/f62e22d0fc1c/c4sc03277b-s3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/905a36cd234f/c4sc03277b-s4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/626c76cb4ecc/c4sc03277b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/3dfb29210735/c4sc03277b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/c392ec5733ea/c4sc03277b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/4a6a3d35aae8/c4sc03277b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/f2fab332512e/c4sc03277b-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/f62e22d0fc1c/c4sc03277b-s3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/905a36cd234f/c4sc03277b-s4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/626c76cb4ecc/c4sc03277b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/3dfb29210735/c4sc03277b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798d/5811104/c392ec5733ea/c4sc03277b-f3.jpg

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