Reaction of functionalised thiols with oligoisobutenes via free-radical addition. Some new routes to thermoplastic crosslinkable polymers

The functionalisation of vinylidene (isopropenyl) terminated oligoisobutenes (polyisobutenes; PIB) with several thiols has been realised in the presence of free-radical generators. Oxygen (air) is a significant accelerator for this reaction and in some cases, alone, is sufficient to cause the reaction to occur. Free-radicals were generated from peroxydicarbonates, AIBN or UV irradiation. The reaction is of an anti-Markovnikov type with the RS-function adding to the vinylidene =CH2 group selectively in the presence of more substituted olefin groups in commercial PIB. A variety of thiols has been investigated and the synthesis of elastomeric polymers resulting from the hydrolysis and condensation of a trialkoxysilane coupled to PIB via a sulphide link has been demonstrated. The synthesis of comb-like polymers made by the addition of PIB to poly(mercaptopropyl methylsiloxane) has been achieved in a way to leave some non-reacted thiol functions available for crosslinking. A perfluoroalkyl thiol modified PIB shows a significant reduction in surface tension compared to the starting PIB polymer. (C) 2003 Elsevier Science Ltd. All rights reserved.