Issue 10, 1997

Surface organometallic chemistry of tin: Thermal transformation, in vacuo, of [triple bond, length as m-dash]Si–O–SnMe3 supported on silica; in situ IR, 13C CP MAS NMR and TPD experiments

Abstract

The thermolysis of [triple bond, length as m-dash]Si–O–SnMe 3 grafted onto partially dehydroxylated silicas has been studied by in situ IR, 13 C CP MAS NMR and TPD. The only detected gaseous product was methane, showing that the thermolysis process passes through a simple hydrolysis reaction between the grafted organometallic fragment and silanol groups. This reaction leads to the formation of ([triple bond, length as m-dash]Si–O) 2 SnMe 2 , ([triple bond, length as m-dash]Si–O) 3 SnMe, and finally tin compounds without organic ligands. The relative proportions of these surface organometallic fragments have been quantitatively determined by three independent methods which gave concordant results. Due to the higher density of hydroxy groups on SiO 2 200, the reactions proceed at a lower temperature on this surface. After thermal treatment at 400 °C, no more methyl ligands remain on the surface and all tin species are probably present as tin(IV) compounds.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans., 1997,93, 1987-1992

Surface organometallic chemistry of tin: Thermal transformation, in vacuo, of [triple bond, length as m-dash]Si–O–SnMe3 supported on silica; in situ IR, 13C CP MAS NMR and TPD experiments

C. Nédez, F. Lefebvre and J. Basset, J. Chem. Soc., Faraday Trans., 1997, 93, 1987 DOI: 10.1039/A607613K

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