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A novel star-shaped cyclotriphosphazene substituted by glycinomethylesterphenoxy and its intermediates are synthesized from hexachlorocyclotriphosphazene (HCCP). The structures are characterized by 1H NMR,13C NMR,31P NMR,FTIR and elemental analysis. Their thermal properties are clarified by thermogravimetric analysis (TGA),differential scanning calorimentry (DSC) and FTIR,while hydrolytic degradation behaviour is studied with UV-vis spectrophotometer and by measuring the weight loss,and the phosphorus content of residue. According to hydrolysis behaviour of hexa[p-(carbonylglycinomethylester)phenoxy]cyclotriphosphazene (HGPCP) under different conditions,it is easy to hydrolyze in hydrochloric acid (pH 1.0) than in phosphate buffer (pH 7.4) at 37℃. And the sample hydrolytic degradation still remains at the stage of side groups’ break. The TGA data show that the thermal stability of the hexa[p-(aldehyde)phenoxy]cyclotriphosphazene (HAPCP),hexa[p-(carboxyl) phenoxy]cyclotriphosphazene (HCPCP) and HGPCP is so high that their char residues are 75%,47% and 47% at 800℃,respectively,probably due to cross-linking between molecules.
A novel star-shaped cyclotriphosphazene substituted by glycinomethylester phenoxy and its intermediates are synthesized from hexachlorocyclotriphosphazene (HCCP). The structures are characterized by 1H NMR, 13C NMR, 31P NMR, FTIR and elemental analysis. Their thermal properties are clarified by thermogravimetric analysis (TGA) , differential scanning calorimentry (DSC) and FTIR, while hydrolytic degradation behavior is studied with UV-vis spectrophotometer and by measuring the weight loss, and the phosphorus content of the residue. According to resistance behavior of hexa [p- (carbonylglycinomethylester) phenoxy] cyclotriphosphazene (HGPCP) under different conditions, it is easy to hydrolyze in hydrochloric acid (pH 1.0) than in phosphate buffer (pH 7.4) at 37 ° C. And the sample hydrolytic degradation still remains at the stage of side groups’ break. The TGA data show that the thermal stability of the hexa [p- (aldehyde) phenoxy] cyclotriphosphazene (HAPCP), hexa [p- (carboxyl) phenoxy] cyclotriphosphazene HCPCP) and HGPCP are so high that their char residues are 75%, 47% and 47% at 800 ° C, respectively, probably due to cross-linking between molecules.