The thermolysis of
![[triple bond, length as m-dash]](https://www.rsc.org/images/entities/char_e002.gif)
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]](https://www.rsc.org/images/entities/char_e002.gif)
Si–O)
2
SnMe
2
, (
![[triple bond, length as m-dash]](https://www.rsc.org/images/entities/char_e002.gif)
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.
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