Abstract
A method for the synthesis of polyphosphosiloxane by the thermal condensation of an equimolar mixture of trimethyl phosphate and (3-aminopropyl)triethoxysilane at 200 °C was developed. The reaction affords ethanol and polyphosphosiloxane-{Si(OEt)[(CH2)3NR1R2]-O-P(O)(OMe)-O}n-(R1 = H, Me; R2 = Me), whose composition and structure were confirmed by 1H, 13C, and 31P NMR spectroscopy, IR spectroscopy, and elemental analysis. The scheme of polymerization involving the intermediate formation of methyl-and dimethylphosphoric acids and their condensation with ethoxysilanes was proposed. The calcination of the obtained polyphosphosiloxane in vacuo at 350 °C results in the elimination of the amino groups and alkoxide substituents, and a spatially cross-linked polymer is formed as an amorphous powder. Its further thermolysis at 600 and 1000 °C gives crystalline phosphosilicates Si5O(PO4)6 or SiP2O7. Their amorphous and crystalline samples were characterized by IR spectroscopy, X-ray diffraction analysis, and solid-state 13C and 31P spectroscopy.