Issue 3, 2012

RuxPtySnzcluster-derived nanoparticlecatalysts: spectroscopic investigation into the nature of active multinuclear single sites

Abstract

Cluster-derived RuxPtySnznanoparticles are active catalysts in the hydrogenation of nitrobenzene. The nature of the active sites has been elucidated by FTIR spectroscopy using CO and NO as probe molecules. A new metal carbonyl cluster precursor, Pt2Ru2(SnBut3)2(CO)9(μ-H)2, has been synthesized to obtain a Ru2Pt2Sn2/SiO2 catalyst, that displayed remarkably high levels of conversion and selectivities compared to other bi-and monometallic analogues. Spectroscopic comparisons with Ru5PtSn/SiO2 indicate that both the nature and the stoichiometry of the metals play a key role in modulating the catalytic activities and selectivities. A multinuclear single-site containing Pt centers, which facilitate the hydrogen activation, coupled with a highly reactive Ru site, possibly involved in the nitrobenzene activation, can be hypothesized. The oxophilicity of tin helps with the anchoring of the nanoparticles, aids the dispersion of the other metals, and can play an important role in influencing the selectivity to aniline.

Graphical abstract: RuxPtySnzcluster-derived nanoparticle catalysts: spectroscopic investigation into the nature of active multinuclear single sites

Supplementary files

Article information

Article type
Paper
Submitted
29 Jun 2011
Accepted
11 Oct 2011
First published
18 Nov 2011

Dalton Trans., 2012,41, 982-989

RuxPtySnzcluster-derived nanoparticle catalysts: spectroscopic investigation into the nature of active multinuclear single sites

M. Manzoli, V. N. Shetti, J. A. L. Blaine, L. Zhu, D. Isrow, V. Yempally, B. Captain, S. Coluccia, R. Raja and E. Gianotti, Dalton Trans., 2012, 41, 982 DOI: 10.1039/C1DT11243K

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