Electro-induced oxidative polymerization of N-vinylcarbazole
✍ Scribed by A. Sezai Saraç; Esma Sezer
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 128 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7147
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✦ Synopsis
In this study, a novel procedure to increase the yield of the non-crosslinked, photoconductive, white form of linear poly(N-vinylcarbazole) (LPVCz) is reported. The yield of LPVCz is increased (up to 53%) by the addition of catalytic amounts of ceric ammonium nitrate as an oxidant during the electrochemical polymerization of Nvinylcarbazole in a divided electrochemical cell. The concentration of Ce(IV) remained constant during the polymerization since Ce(III) is readily oxidized to Ce(IV) electrochemically. Since the electrochemical oxidation of Ce(III) to Ce(IV) took place simultaneously at the anode, the deposition of dark green crosslinked polyvinylcarbazole on the electrode surface, which hinders the formation of white LPVCz, can be prevented. The Fourier transform infrared, ultraviolet±visible and fluorescence spectra of white LPVCz showed that the structures of polymers are the same as those produced by conventional polymerization.
📜 SIMILAR VOLUMES
Poly (N-vinylcarbazole), poly(N-carbazole) and poly(Nethylcarbazole) powders were chemically synthesized by the reaction of ceric ammonium nitrate (CAN) with N-vinylcarbazole carbazole and N-ethylcarbazole in acetonitrile. Products were characterized by elemental analysis, Fourier transform infrared
In this communication, we first used [60]fullerene as initiator to initiate the bulk polymerization of N-vinylcarbazole (NVC) monomer at 70°C (slightly higher than the melting point temperature, 65°C, of NVC). A reasonable polymerization reaction pathway via C 60 -NVC ion-radical pairs is suggested.