Issue 3, 2015

A highly efficient and reusable MCM-41-immobilized bipyridine copper(i) catalyst for the C–Se coupling of organoboronic acids with diaryl diselenides

Abstract

A highly efficient MCM-41-immobilized bipyridine copper(I) complex [MCM-41-bpy-CuI] was prepared from 4,4′-bis[3-(triethoxysilyl)propylaminomethyl]-2,2′-bipyridine via immobilization on the mesoporous material MCM-41, followed by reaction with CuI. In the presence of 5 mol% MCM-41-bpy-CuI, the cross-coupling reaction of organoboronic acids with diaryl diselenides proceeded smoothly in DMSO/H2O (2/1) at 110 °C under air to afford a variety of diorganyl selenides in good to excellent yields. This heterogeneous copper catalyst can be recovered and recycled by a simple filtration of the reaction solution and used for at least 10 consecutive trials without any decrease in activity.

Graphical abstract: A highly efficient and reusable MCM-41-immobilized bipyridine copper(i) catalyst for the C–Se coupling of organoboronic acids with diaryl diselenides

Supplementary files

Article information

Article type
Paper
Submitted
30 Sep 2014
Accepted
07 Jan 2015
First published
08 Jan 2015

New J. Chem., 2015,39, 2106-2115

A highly efficient and reusable MCM-41-immobilized bipyridine copper(I) catalyst for the C–Se coupling of organoboronic acids with diaryl diselenides

H. Zhao, Y. Jiang, Q. Chen and M. Cai, New J. Chem., 2015, 39, 2106 DOI: 10.1039/C4NJ01687D

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