Novel Copolymers of Styrene. 18. Halogen Ring-Trisubstituted Methyl 2-Cyano-3-Phenyl-2-Propenoates

التفاصيل البيبلوغرافية
العنوان: Novel Copolymers of Styrene. 18. Halogen Ring-Trisubstituted Methyl 2-Cyano-3-Phenyl-2-Propenoates
المؤلفون: Hui Feng, Ahlam Shahbain, Sara M. Rocus, Gregory B. Kharas, Teresa Spann, Hemal S. Bhavsar, William S. Schjerven
المصدر: Journal of Macromolecular Science, Part A. 52:90-94
بيانات النشر: Informa UK Limited, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Ethylene, Polymers and Plastics, Chemistry, General Chemistry, Styrene, chemistry.chemical_compound, Monomer, Polymer chemistry, Materials Chemistry, Ceramics and Composites, Copolymer, Reactivity (chemistry), Knoevenagel condensation, Piperidine, Polystyrene
الوصف: Novel trisubstituted ethylene monomers, halogen ring-trisubstituted methyl 2-cyano-3-phenyl-2-propenoates, RPhCH=C(CN)CO2CH3, where R is 4-bromo-2,6-difluoro, 3-chloro-2,6-difluoro, 4-chloro-2,6-difluoro, 2,3,5-trichloro, 2,3,6-trichloro, and 2,4,5-trifluoro, were prepared and copolymerized with styrene. The monomers were synthesized by the piperidine catalyzed Knoevenagel condensation of halogen ring-trisubstituted benzaldehydes and methyl cyanoacetate, and characterized by CHN analysis, IR, 1H and 13C-NMR. All the ethylenes were copolymerized with styrene (M1) in solution with radical initiation (ABCN) at 70°C. The compositions of the copolymers were calculated from nitrogen analysis and the structures were analyzed by IR, 1H and 13C-NMR. The order of relative reactivity (1/r1) for the monomers is 3-Cl-2,6-F2 (4.2) > 4-Cl-2,6-F2 (3.9) > 4-Br-2,6-F2 (1.8) > 2,3,5-Cl3 (1.1) > 2,4,5-F3 (0.9) > 2,3,6-Cl3 (0.5). Relatively high Tg of the copolymers in comparison with that of polystyrene indicates a decrease ...
تدمد: 1520-5738
1060-1325
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b8e9da997c77ba8bd6430e60c190b713
https://doi.org/10.1080/10601325.2015.980712
رقم الأكسشن: edsair.doi...........b8e9da997c77ba8bd6430e60c190b713
قاعدة البيانات: OpenAIRE