Issue 8, 2013

Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium

Abstract

Functionalized flower-like mesoporous silica with a chiral organorhodium functionality incorporated within its silica framework is prepared through an assembly of chiral 4-((trimethoxysilyl)ethyl)phenylsulfonyl-1,2-diphenylethylenediamine and tetraethoxysilane under a cooperative dual-template approach followed by complexation with organorhodium complexes. Structural characterization discloses its mesostructure and well-defined single-site chiral organorhodium functionality, while electron microscopy analyses reveal the uniformly distributed three-dimensional spherical flowers constructed by the stacking of leaf-shaped nanoflakes. In particular, as a bifunctionalized heterogeneous catalyst, it shows excellent catalytic activity and high enantioselectivity in the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium (more than 99% conversion and up to 97% ee). The superior catalytic performance is attributed to the synergistic effect of the salient cetyltrimethylammonium bromide phase-transfer function and confined chiral organorhodium catalytic nature. Furthermore, this heterogeneous catalyst could be recovered easily and reused repeatedly (ten times) without affecting its ee value, showing a practical application in asymmetric synthesis.

Graphical abstract: Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium

Supplementary files

Article information

Article type
Paper
Submitted
23 Mar 2013
Accepted
13 May 2013
First published
13 May 2013

Green Chem., 2013,15, 2208-2214

Flower-like mesoporous silica: a bifunctionalized catalyst for rhodium-catalyzed asymmetric transfer hydrogenation of aromatic ketones in aqueous medium

F. Gao, R. Jin, D. Zhang, Q. Liang, Q. Ye and G. Liu, Green Chem., 2013, 15, 2208 DOI: 10.1039/C3GC40547H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements