Issue 19, 1999

Spectroscopic and thermodynamic study of the H-bonding of olefins onto the isolated hydroxyl of amorphous silica

Abstract

FTIR data are reported concerning the adsorption of ethene, propene, but-1-ene, trans-but-2-ene, cyclohexene and methylcyclohexene on Aerosil outgassed at 800°C. H-bonding is the only process occurring with the four lighter molecules, and a strictly Langmuir-type behaviour is found. With the two heavier species, plain physisorption also takes place, causing the solvation of H-bonded adducts, which are best defined at low coverage. From the intensity of the ν(OH) mode of the free hydroxyls as a function of pressure, the equilibrium constant for the H-bond formation is calculated in different ways, according to the role of physisorption. Several correlations are drawn for Δν(OH) and ΔG°. The contribution of the substituents to the basicity of the double bond as measured by the shift in frequency is discussed, as well as the role of H-bonding and van der Waals forces in dictating the energetics of the interaction.

Article information

Article type
Paper

Phys. Chem. Chem. Phys., 1999,1, 4649-4654

Spectroscopic and thermodynamic study of the H-bonding of olefins onto the isolated hydroxyl of amorphous silica

E. Garrone, A. Barbaglia, B. Onida, B. Civalleri and P. Ugliengo, Phys. Chem. Chem. Phys., 1999, 1, 4649 DOI: 10.1039/A903682B

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