Issue 34, 2017, Issue in Progress

One-pot redox synthesis of Pt/Fe3O4 catalyst for efficiently chemoselective hydrogenation of cinnamaldehyde

Abstract

External additives (i.e., ionic electride donors) are usually necessary to obtain a high catalytic performance in an electron-density-dependent chemoselective hydrogenation reaction. Here, a sphere-shaped Pt/Fe3O4 catalyst is prepared through a one-pot redox reaction using Pt(IV) and Fe(II) precursors. The experimental results show that the prepared Pt/Fe3O4 catalyst with an Fe to Pt mole ratio of 100 : 1 can afford a high conversion of 94.2% towards cinnamaldehyde (CAL) and good selectivity of 92.2% towards cinnamyl alcohol (COL) under the mild conditions of 303 K, 5 bar H2 for 150 min in the chemoselective reduction of CAL. The excellent catalytic performance could be attributed to the dissociation of H2 and adsorption of CAL via a vertical configuration modulated by the electronic effect between Pt and Fe3O4, and the abundant available active sites induced by uniformly dispersed Pt nanoparticles. Additionally, the intrinsic magnetism of Fe3O4 nanospheres endows the catalyst with a rapid separation property, favourable for repeated use of a catalyst.

Graphical abstract: One-pot redox synthesis of Pt/Fe3O4 catalyst for efficiently chemoselective hydrogenation of cinnamaldehyde

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2017
Accepted
06 Apr 2017
First published
12 Apr 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 21107-21113

One-pot redox synthesis of Pt/Fe3O4 catalyst for efficiently chemoselective hydrogenation of cinnamaldehyde

Y. Zhang, C. Chen, W. Gong, J. Song, Y. Su, H. Zhang, G. Wang and H. Zhao, RSC Adv., 2017, 7, 21107 DOI: 10.1039/C7RA02898A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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