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Synthesis and properties of PBO precursors having bulky groups and ether linkages in the main chain  

Yoon, Doo-Soo (Dept. of Polymer Science & Engineering, Chosun University)
Kim, Hee-Sun (Dept. of Polymer Science & Engineering, Chosun University)
Choi, Jae-Kon (Dept. of Polymer Science & Engineering, Chosun University)
Hong, Wan-Hae (Dept. of Chemical Engineering, Chosun University)
Publication Information
Elastomers and Composites / v.43, no.4, 2008 , pp. 271-280 More about this Journal
Abstract
Aromatic polyhydroxyamides (PHAs) having bulky groups and ether linkages in the polymer main chain were synthesized by the low temperature solution polycondensation reaction. FT-IR, $^{1}H-NMR$, DSC, and TGA were used to study the properties of these polymers. The PHAs were converted into polybenzoxazoles (PBOs) by a thermal cyclization reaction, and endothermic peaks were observed in the range of $220{\sim}400^{\circ}C$. The introduction of the ether and bulky groups in the main chain improved the solubility of the PHAs in aprotic solvents such as DMSO and DMF, but the PBOs were nearly insoluble in common solvents. All the PBOs, except for PBO 5 with 2,6-dimethylphenoxy pendant and 2,3-dihydroxyquinoxaline ring, and PBO 6 with 2,6-dimethylphenoxy pendant and 2,3-dihydroxyquinoxaline ring, exhibited $T_g in the range from 149 to $217^{\circ}C$ by DSC. The thermogravimetric analyses indicated that most of the PBOs were thermally stable up to $400^{\circ}C$ in nitrogen. Maximum weight loss temperatures of PHA 5 and PBO 5 with 2,6-dimethylphenoxy pendant and 2,3-dihydroxyquinoxaline ring were $707^{\circ}C$ and $683^{\circ}C$, respectively, which were the hightest temperatures among the corresponding copolymers. The PBOs in nitrogen exhibited relatively high char yields in the range of $63{\sim}70%$ at $900^{\circ}C$.
Keywords
polyhydroxyamides; polybenzoxazoles; copolymerization; thermal cyclization reaction;
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