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

Chem Sci

Materials Research Center for Element Strategy , Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku , Yokohama 226-8503 , Japan . Email: ; Email:

Published: September 2016

AI Article Synopsis

  • The study explores a new method to enhance catalytic activity by using a stable electride combined with bimetallic nanoparticles, specifically a Ru-Fe nano-alloy.
  • The electride [CaAlO]·(e) has a low work function, increasing the catalyst's effectiveness in converting α,β-unsaturated aldehydes to unsaturated alcohols without the need for solvents.
  • The synergistic effect between the electride and the nanoparticles allows for better H dissociation and the preferred adsorption of specific chemical bonds, making it possible to produce valuable chemicals that are otherwise difficult to obtain.

Article 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 [CaAlO]·(e), 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 H 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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022174PMC
http://dx.doi.org/10.1039/c6sc01864eDOI Listing

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