Cyclomethicone
A siloxane is a functional group in organosilicon chemistry with the Si–O–Si linkage. The parent siloxanes include the oligomeric and polymeric hydrides with the formulae H(OSiH2)nOH and (OSiH2)n. Siloxanes also include branched compounds, the defining feature of which is that each pair of silicon centres is separated by one oxygen atom. The siloxane functional group forms the backbone of silicones, the premier example of which is polydimethylsiloxane. The functional group (RO)3Si is called siloxy.
Siloxanes generally adopt structures expected for linked tetrahedral ("sp3-like") centers. The Si–O bond is 1.64 Å (vs Si–C distance of 1.92 Å) and the Si–O–Si angle is rather open at 142.5°. By way of contrast, the C–O distance in a typical dialkyl ether is much shorter at 1.414(2) Å with a more acute C–O–C angle of 111°. It can be appreciated that the siloxanes would have low barriers for rotation about the Si–O bonds as a consequence of low steric hindrance. This geometric consideration is the basis of the useful properties of some siloxane-containing materials, such as their low glass transition temperatures.
The main route to siloxane functional group is by condensation of two silanols:
Usually the silanols are generated in situ by hydrolysis of silyl chlorides. With a disilanol, R2Si(OH)2 (derived from double hydrolysis of a silyldichloride), the condensation can afford linear products terminated with silanol groups:
Alternatively the disilanol can afford cyclic products
Starting from trisilanols, cages are possible, such as the species with the formula (RSi)nO3n/2 with cubic (n = 8) and hexagonal prismatic (n = 12). (RSi)8O12 structures. The cubic cages are cubane-type clusters, with silicon centers at the corners of a cube oxygen centres spanning each of the twelve edges.
Oxidation of organosilicon compounds, including siloxanes, gives silicon dioxide. This conversion is illustrated by the combustion of hexamethylcyclotrisiloxane:
...
Wikipedia