1,5-hydrogen transfer — a hitherto ignored decay channel in the photodegradation of poly(2,6-dimethyl-1,4-phenylene oxide)
✍ Scribed by Siegfried Schneider; Peter Gedeck; Josef Harrer; Frauke Richter; Timothy Clark
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 401 KB
- Volume
- 257
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
We present the results of a theoretical study and put forward a novel mechanism for the photodegradation of the polymer poly(2,6-dimethyl-l,4-phenylene oxide) (PPE). The primary step is a 1,5-hydrogen transfer from the methyl group of one ring system to the ipso-earbon of the adjacent monorneric unit. Therefore, in contrast to other proposed mechanisms, the primary step is a result of the three-dimensional structure of PPE rather than a consequence of structural defects in the polymer chain or of impurities.
📜 SIMILAR VOLUMES
## Abstract **Summary:** A novel approach of in situ polymerization and in situ compatibilization was adopted to prepare poly(2,6‐dimethyl‐1,4‐phenylene oxide) (PPO) and polyamide 6 (PA6) nanoblends. Anionic ring‐opening polymerization of __ε__‐caprolactam was carried out in the presence of PPO, th
Molecular relaxation behavior in terms of the a, b, and g transitions of miscible PS/PPO blends has been studied by means of DMTA and preliminary work has been carried out using DSC. From DSC and DMTA (by tan d), the observed a relaxation ( T a or T g ) of PS, PPO, and the blends, which are intermed
The oxidation of Ix)ly ( 2,6-dimethyl-C, 4-phenylene ether) (PPE) during polymerization has been examined as a function of molecular weight, using spectroscopic techniques. The visible light absorption and the IR absorption at 1660cm -I increased as the molecular weight decreased. A most probable ch