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• W2428172092 endingPage "2819" @default.
• W2428172092 startingPage "2811" @default.
• W2428172092 abstract "A trifunctional benzoxazine, 1,3,5-tris(3-phenyl-3,4-dihydro-2H-benzo[1,3]oxazin-6-yl)benzene (T-Bz) was synthesized and in an effort to reduce its curing temperature (curing maxima at 238 °C), it was mixed with various phenolic nucleophiles such as phenol (PH), p-methoxy phenol (MPH), 2-methyl resorcinol (MR), hydroquinone (HQ), pyrogallol (PG), 2-naphthol (NPH), 2,7-dihydroxy naphthalene (DHN), and 1,1'-bi-2-naphthol (BINOL). The influence of these phenolic nucleophiles on ring-opening polymerization temperature of T-Bz was examined by DSC and FTIR analysis. T-Bz undergoes a complete ring-opening addition reaction in the presence of bi- and trifunctional phenolic nucleophiles (MR/HQ/PG/DHN) at 140 °C (heated for 3 h) and forms a networked polybenzoxazine (NPBz). The NPBzs showed a high thermal stability with Td20 of 350–465 °C and char yield of 67–78% at 500 °C; however, a diminutive weight loss (6.9–9.8%) was observed at 150–250 °C (Td5: 215–235 °C) due to degradation of phenolic end groups. This article also gives an insight on how the traces of phenolic impurities can alter the thermal properties of pure benzoxazine monomer as well as its corresponding polymer. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 2811–2819" @default.
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• W2428172092 date "2016-06-18" @default.
• W2428172092 modified "2023-09-29" @default.
• W2428172092 title "Synthesis of novel tri-benzoxazine and effect of phenolic nucleophiles on its ring-opening polymerization" @default.
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• W2428172092 doi "https://doi.org/10.1002/pola.28167" @default.
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