Silica hydride intermediate for octadecylsilica and phenyl bonded phase preparation via heterogeneous hydrosilation in supercritical carbon dioxide

• Published in: Journal of Chromatography A 2011-04, Vol.1218 (15), p.1974-1982
• Main Authors: Scully, N.M., Ashu-Arrah, B.A., Nagle, A.P., Omamogho, J.O., O'Sullivan, G.P., Friebolin, V., Dietrich, B., Albert, K., Glennon, J.D.
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Bonding; Carbon dioxide; Chemistry; Chromatographic methods and physical methods associated with chromatography; chromatography; Conversion; dioxane; Endcapping; Exact sciences and technology; Green chemistry; Hydrides; Hydrosilation; nuclear magnetic resonance spectroscopy; Other chromatographic methods; Reaction time; silica; Silica hydride; Silicon dioxide; Solvents; spectral analysis; styrene; Supercritical carbon dioxide; Supercritical fluids; Supercritical functionalisation; temperature; toluene
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2010.11.046

Investigations into the preparation of silica hydride intermediate in supercritical carbon dioxide (sc-CO 2) that avoids the use of organic solvents such as toluene or dioxane are described. The effects of reaction temperature, pressure and time on the surface coverage of the supercritical fluid generated silica hydride intermediate were studied. Under optimised supercritical conditions of 120 °C, 483 bar and 3 h reaction time, silica hydride (Si–H) conversion efficiencies of ca. 40% were achieved for the hydride intermediate prepared from a monofunctional silane reagent (dimethylmethoxysilane). Si–H conversion efficiencies (as determined from 29Si CP-MAS NMR spectral analysis) for the hydride intermediate prepared from triethoxysilane (TES) in sc-CO 2 were found to be comparable to those obtained using a TES silanisation approach in an organic solvent. 13C and 29Si CP-MAS-NMR spectroscopy was employed to provide a complete structural assignment of the silica hydride intermediates. Furthermore, supercritical CO 2 was subsequently employed as a reaction medium for the heterogenous hydrosilation of silica hydride with octadecene and with styrene, in the presence of a free radical initiator. These supercritical fluid generated reversed-phase materials were prepared in a substantially reduced reaction time (3 h) compared to organic solvent based methods (100 h reaction time). Silica functionalisation in sc-CO 2 presents an efficient and clean alternative to organic solvent based methods for the preparation of important silica hydride intermediate and silica bonded stationary phases via a hydrosilation approach.