Q.If the starting material for the manufacture of silicones is RSiCl3, write the structure of the product formed.
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Start your 14-day free trial to unlock the full solution →RSiCl's three chlorines each hydrolyse to –OH, and because all three condense with neighbouring units, the polymer that forms is cross-linked (3-D network), unlike the linear chains RSiCl would give.
- Hydrolysis of RSiCl. In moist air/water, each Si–Cl bond is hydrolysed to Si–OH:
This gives a silanol, RSi(OH), with three –OH groups on each silicon (i.e. RSiCl is "trifunctional").
- Condensation polymerisation. These silanol units then undergo intermolecular condensation: an –OH on one silicon reacts with an –OH on a neighbouring silicon, eliminating a water molecule and forming an Si–O–Si linkage:
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Why the product is cross-linked (3-D), not linear. Because each silicon atom retains three –OH groups (after losing only one Cl-derived bond to its own R group), it can condense with up to three different neighbouring silicon atoms — one Si can therefore branch out to link with three others rather than just two, as would be the case for the difunctional RSiCl (which gives simple linear chains). This trifunctional linking builds a cross-linked, three-dimensional (sheet-like/network) silicone structure.
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Resulting structure. Each silicon atom sits at a branch point, bonded to its own R group and to three oxygen bridges connecting it to neighbouring silicon atoms, each of which is in turn bonded to its own R group and further oxygen bridges — extending indefinitely into a cross-linked polymer: …
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