Issue 9, 2016

Electronic interactions between a stable electride and a nano-alloy control the chemoselective reduction reaction

Abstract

Controlling the electronic structure of heterogeneous metal catalysts is considered an efficient method to optimize catalytic activity. Here, we introduce a new electronic effect induced by the synergy of a stable electride and bimetallic nanoparticles for a chemoselective reduction reaction. The electride [Ca24Al28O64]4+·(e)4, with extremely low work function, promotes the superior activity and selectivity of a Ru–Fe nano-alloy for the conversion of α,β-unsaturated aldehydes to unsaturated alcohols in a solvent-free system. The catalyst is easily separable from the product solution and reusable without notable deactivation. Mechanistic studies demonstrate that electron injection from the electride to the Ru–Fe bimetallic nanoparticles promotes H2 dissociation on the highly charged active metal and preferential adsorption of C[double bond, length as m-dash]O bonds over C[double bond, length as m-dash]Cs bond of the unsaturated aldehydes, to obtain the thermodynamically unfavorable but industrially important product.

Graphical abstract: Electronic interactions between a stable electride and a nano-alloy control the chemoselective reduction reaction

Supplementary files

Article information

Article type
Edge Article
Submitted
28 Apr 2016
Accepted
20 May 2016
First published
24 May 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 5969-5975

Electronic interactions between a stable electride and a nano-alloy control the chemoselective reduction reaction

T. Ye, J. Li, M. Kitano, M. Sasase and H. Hosono, Chem. Sci., 2016, 7, 5969 DOI: 10.1039/C6SC01864E

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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