Abstract
The four-step preparation of a new monomer, 1,2,3-tris(4-cyanatophenoxy)-,3′,5,5-tris-phenoxy-2λ5,4λ5,6λ5-[1,3,5,2,4,6]-triazatriphosphinine, is reported. Characterization of the monomer is undertaken using spectroscopic and chromatographic methods and elemental analysis and the data are in agreement with the proposed structure (as a mixture of isomers). The thermal polymerization of the monomer and its behaviour within selected blends containing 2,2-bis(4-cyanatophenyl)propane (AroCy B10) are studied using differential scanning calorimetry. The blends appear to melt sharply at ca. 80 °C onset of polymerization (corresponding to the melting point of the commercial dicyanate) before commencing polymerization directly thereafter. Typical exothermic peak maxima at ca. 135 °C are observed, whilst the cure is apparently concluded by 200 °C under the scanning conditions. On rescan, the cured samples display glass transition values in the region of 160–190 °C, depending on composition with the higher values reflecting increasing amounts of the new material. The cured polycyanurate of the tricyclophosphazene is also analysed using thermogravimetric analysis and displays a mass loss of 5% at approximately 381 °C in air and 366 °C in nitrogen. When 1,2,3-tris(4-cyanatophenoxy)-,3′,5,5-tris-phenoxy-2λ5,4λ5,6λ5-[1,3,5,2,4,6]-triazatriphosphinine is combined with AroCy B10, the cured copolymers (containing between 10 and 30 wt% of the tricyclophosphazene) show disappointing thermal stability with a progressive reduction in the onset of degradation with increasing phosphazine content; this may be a result of incomplete cure.