کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1524207 | 995335 | 2012 | 9 صفحه PDF | دانلود رایگان |

Up to date, only a few kinds of poly(azomethine-urethane)s (PAMUs) were synthesized and studied with thermal degradation steps. However, polyphenol based PAMUs including azomethine linkages have not been investigated yet. The polyurethanes were prepared by condensation reaction of 2,4-dihydroxybenzaldehyde (2,4-DHBA) with toluene-2,4-diisocyanate (TDI) under argon atmosphere. Synthesized polyurethane was converted to its poly(azomethine urethane) species (TP-2AP, TP-3AP, and TP-4AP) by graft copolymerization reactions with amino phenols (2-amino phenol, 3-amino phenol, and 4-amino phenol). Obtained poly(azomethine urethane)s were converted to their polyphenol species (P-TP-2AP, P-TP-3AP, and P-TP-4AP) by oxidative polymerization reaction (OP) using NaOCl as the oxidant. The structures of the obtained compounds were confirmed by FT-IR, UV–vis, 1H NMR, and 13C NMR techniques. The molecular weight distribution parameters of the synthesized compounds were determined by the size exclusion chromatography (SEC). The synthesized compounds were also characterized by solubility tests, TG-DTA, and DSC. Fluorescence measurements were carried out in various concentrated DMF solutions to determine the optimum concentrations to obtain the maximal PL intensities.
▶ Synthesis, characterization, and thermal stability of novel poly(azomethine-urethane)s and polyphenol derivatives derived from 2,4-dihydroxy benzaldehyde and toluene-2,4-diisocyanate.Figure optionsDownload as PowerPoint slideHighlights
► New pol(azomethine-urethane)s were synthesized.
► PAMUs were converted to their polyphenol species by oxidative polymerization reaction with NaOCl.
► The synthesized compounds were characterized by solubility tests, TGA and DSC.
► Tg values of PAMUs were between 137 and 178 °C and thermal stabilities of them were very good.
► Obtained compounds can be promising candidates for aerospace applications.
Journal: Materials Chemistry and Physics - Volume 133, Issue 1, 15 March 2012, Pages 269–277