A new aromatic sulfone ether diamine was synthesized by nucleophilic aromatic substitution reaction of 5-amino-1-naphthol with bis(4-chlorophenyl) sulfone in the presence of potassium carbonate in a polar aprotic solvent. Polycondensation reactions of the obtained diamine with pyromellitic dianhydri
Synthesis and thermal properties of thermosetting bis-benzocyclobutene–terminated arylene ether monomers
✍ Scribed by Loon-Seng Tan; N. Venkatasubramanian; Patrick T. Mather; Marlene D. Houtz; Charles L. Benner
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 396 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
A series of new bis-benzocyclobutene-endcapped arylene ether monomers was prepared and characterized. Whereas 2,6-bis(4-benzocyclobutenyloxy)benzonitrile (BCB-EBN) could be prepared in good yield using the standard procedure (K 2 CO 3 / NMP/toluene/Dean-Stark trap/120°C), other bis(benzocyclobutene) (BCB)-terminated monomers containing ether-benzophenone (BCB-EK), ether-phenylsulfone (BCB-ES), and ether-6F-benzoxazole (BCB-EBO) moieties were invariably contaminated by monoendcapped products under similar reaction conditions. This can be attributed to a much greater activating effect of the nitrile group on the ortho-fluorides in the aromatic nucleophilic displacement reaction than the carbonyl, sulfonyl, and benzoxazolyl groups. However, the latter monomers could be synthesized (70 -80%) from 4-trimethylsiloxybenzocyclobutene and respective aromatic fluorides in the presence of CsF at 140°C. Similar curing behaviors under N 2 (DSC: extrapolated onset and peak temperatures at 227-230°and 260 -262°C, respectively) characterized all four monomers. BCB-EK, BCB-ES, and BCB-EBN showed melting transitions at 108, 119, and 146°C, in that order. As BCB-EBO contained more rigid benzoxazole segments, it only exhibited a glass transition (T g ) at 85°C prior to curing exotherm, after it had been previously heated to 125°C. The following T g s were observed for the cured materials: BCB-EK (201°C), BCB-EBN (224°C), BCB-ES (264°C), and BCB-EBO (282°C). The relative thermal stability according to TGA (He) results is: BCB-ES Ͻ BCB-EBN Ͻ BCB-EK Ͻ BCB-EBO. Finally, the results from thermal analysis, infrared spectroscopic, and variable temperature microscopic studies indicated that the nitrile group plays an important role in the cure chemistry, thermal, and microstructural properties of BCB-EBN.
📜 SIMILAR VOLUMES
A series of novel poly(arylene ether ketone)s were synthesized from the reaction of hydroquinone and 4-(4-hydroxyphenyl)-2,3-phthalazin-1-one with 4,4Ј-difluorobenzophenone in N-cyclohexylpyrrolidinone containing anhydrous potassium carbonate. The polymers exhibited high glass transition temperature