Issue 2, 2014

The synthesis of multiphasic ionic liquid-coated Pt/Al2O3 catalysts: the selective synchronous hydrogenation of C[double bond, length as m-dash]C and C[double bond, length as m-dash]O bonds and the modeling of the ionic liquid and solvent effects

Abstract

Various ionic liquids (ILs) and their mixtures were coated on the Pt/Al2O3 catalyst and the resulting IL-coated catalysts were used in the synchronous hydrogenation of cyclohexene and acetone. The rate constant (k) and selectivity (S) toward C[double bond, length as m-dash]O hydrogenation were determined for several catalysts in various solvents. The solvatochromic parameters (ETN, normalized polarity parameter; π*, dipolarity–polarizability; β, hydrogen-bond acceptor basicity; α, hydrogen-bond donor acidity) were determined for the used ILs and solvents and the obtained selectivities were modeled based on the solvatochromic parameters of the IL layer and bulk solvent while using the Multiparameter Linear Regression (MLR) method for the first time. Selectivity toward the C[double bond, length as m-dash]O bond increases by increasing the percentage of 2-hydroxy ethylammonium formate (HEAF) in the IL layer and decreasing the polarity of the solvents. The single-parameter correlations of lnS versus π* presented the best correlation for the prepared catalysts in all solvents.

Graphical abstract: The synthesis of multiphasic ionic liquid-coated Pt/Al2O3 catalysts: the selective synchronous hydrogenation of C [[double bond, length as m-dash]] C and C [[double bond, length as m-dash]] O bonds and the modeling of the ionic liquid and solvent effects

Article information

Article type
Paper
Submitted
17 Jul 2013
Accepted
15 Oct 2013
First published
17 Oct 2013

Catal. Sci. Technol., 2014,4, 447-455

The synthesis of multiphasic ionic liquid-coated Pt/Al2O3 catalysts: the selective synchronous hydrogenation of C[double bond, length as m-dash]C and C[double bond, length as m-dash]O bonds and the modeling of the ionic liquid and solvent effects

R. V. Meidanshahi, M. Tasviri, M. Khodadadi-Moghaddam and M. R. Gholami, Catal. Sci. Technol., 2014, 4, 447 DOI: 10.1039/C3CY00510K

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