## Abstract We prepared triphenylamine (TPA)βcontaining polymers by a direct oxidativeβcoupling method, which showed high thermostability, good solubility, high quantum efficiency, and blue light emission. The polymers are characterized by Fourier transform infrared spectroscopy, ^1^HβNMR, ultravio
On the structure of macromolecules obtained by oxidative polymerization of polyhydroxyphenols and quinones
β Scribed by Cataldo, Franco
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 187 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
The chemical structure of synthetic humic acid or synthetic melanin, obtained by oxidative polymerization of hydroquinone or para-benzoquinone in alkali solutions was determined by means of elemental analysis, 1H NMR, electronic and FTIR spectroscopies, and by high temperature zinc dust treatment. The shiny black material obtained was proved to be a poly(hydroxyhydroquinone-co-hydroxybenzoquinone) having the monomeric units connected at the ortho position and hence having a poly(ortho-phenylene) backbone instead of the other possible structure with a poly(para-phenylene) backbone. The chemical similarity between this synthetic humic acid and natural humic acids and natural melanins is discussed.
1998 SCI.
π SIMILAR VOLUMES
Oxidative polymerization of m-phenylenediamine was carried out using H 2 O 2 as an oxidant and horseradish peroxidase as a catalyst in mixtures of aqueous buffer solution and 1,4-dioxane or in reversed micellar solutions. When the reaction mixture was brought into contact with a stainless steel stic