The conversion of the precursor into poly(phenylenevinylene) (PPV) was studied by means of photoelectron spectroscopy (XPS) and electron spin resonance (ESR) on precursor films synthesized from the polymerization of pxylene-tetrahydrophenium halides. The sulfonium precursor containing chlorine or br
The thermal conversion of the tetrahydrothiophene-precursor polymer to poly(p-phenylene vinylene)
β Scribed by M. Herold; J. Gmeiner; M. Schwoerer
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 337 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7147
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β¦ Synopsis
This paper reports the thermal conversion of the tetrahydrothiophene (THT)-precursor to poly(p-phenylene vinylene) (PPV). Detailed investigations of the conversion process show that the leaving groups THT and HCl do not eliminate simultaneously. Moderate temperatures ( 125 Β°C) are sufficient to eliminate the THT while a higher temperature of %150 Β°C is necessary for the leaving group HCl. Furthermore, the THT groups split off at two characteristic temperatures. Our investigations have shown that a consistent picture of the reaction mechanism can only be obtained if the configuration of the polymer chain is considered. For the total reaction of the THT-precursor to PPV a reaction mechanism is suggested that consists of at least four steps.
π SIMILAR VOLUMES
The use of sulfinyl groups as thermally eliminable groups in precursor routes towards poly(para-phenylene vinylene), PPV is relatively new and has not yet been fully explored. In this paper the elimination of sulfinyl groups in a sulfinyl precursor, poly[1,4-phenylene (1-n-alkyl sulfinyl)-ethylene],