Abstract
The reaction of γ-aminopropylorganosiloxanes with phenolphthalein yields monomeric and oligomeric N-alkylsiloxy-3,3-bis(4-hydroxyphenyl)phthalimidines. Their structures and compositions were confirmed by IR and NMR spectroscopy and by HPLC-MS. Studies by GLC and MALDI mass spectrometry showed that the action of the amine and of the water released in the reaction leads to the rearrangement of the siloxane bond in the course of the synthesis with the formation of linear and cyclic carbofunctional oligomeric siloxanephenols and mixed oligophenolaminosiloxanes. The possibility of modification of epoxy resins with the synthesized oligomers was revealed.
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