| Titolo | Diastereotopic styrene arrangement in the heterosequences of random styrene-ethylene copolymers |
|---|---|
| Tipo di pubblicazione | Articolo su Rivista peer-reviewed |
| Anno di Pubblicazione | 2008 |
| Autori | Longo, P., Napoli M., and Ricciardi Rosa |
| Rivista | Macromolecular Chemistry and Physics |
| Volume | 209 |
| Paginazione | 1050-1055 |
| ISSN | 10221352 |
| Parole chiave | ABS resins, Butadiene, Complexation, Copolymerization, Copolymers, Diffraction, Ethylene, Ethylene copolymers, Fourier transform infrared spectroscopy, Fourier transforms, FTIR spectrums, Glass transition, Intermediate temperatures, Isotactic, Methine, Methylene carbons, Model compounds, NMR, Nmr spectroscopies, Nuclear magnetic resonance, Nuclear magnetic resonance spectroscopy, Pentadecane, Phenyl groups, Phenyl substituents, Plastic products, Polymers, Polystyrenes, Powder diffractions, Powders, Resonance, Single glass transitions, Stereoregularity, styrene, Synthesis of, thermal analysis, Thermoanalysis, X ray diffraction analysis |
| Abstract | {Random styrene-ethylene copolymers have been synthesized by the hydrogenation of styrene-butadiene copolymers. The samples were characterized by 13C NMR spectroscopy, X-ray powder diffraction, thermal analysis, and Fourier transform IR (FTIR) spectroscopy. In the 13C NMR spectra, the resonance of the methylene carbon next to a methine bearing a phenyl group presents splitting due to its diastereotopic positions with respect to the phenyl substituents of the second and third inserted styrene units. A definitive assignment of the resonances of the SEES sequences (S = styrene |
| Note | cited By 0 |
| URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-55349142495&doi=10.1002%2fmacp.200800007&partnerID=40&md5=985459dea6ac6d99af3418ac145a940c |
| DOI | 10.1002/macp.200800007 |
| Citation Key | Longo20081050 |
