Ortho-, meta-, and para-phenylenediamines were polymerized using hydrogen peroxide as an oxidant and horseradish peroxidase as a catalyst in mixed solvents of 1,4-dioxane and water. The yield of the polymers was strongly dependent on solvent composition, and maximum yields were obtained at 15-30% 1,
Oxidative polymerization of phenylenediamines by enzyme and magnetic properties of the products
โ Scribed by Daigo Ichinohe; Toshitaka Muranaka; Hideo Kise
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 145 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
โฆ Synopsis
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 stick, the obtained polymer responded to a permanent magnet at room temperature in the air. From the ICP emission spectroscopic analysis, it was found that these polymers contained small amounts of transition metals, such as Fe and Ni. The magnetic properties of the obtained polymers were studied with a superconducting quantum interference device (SQUID). The M (magnetization)-H (magnetic field) curves showed sigmoid behavior at 300 K, but did not exhibit a residual magnetization and a coercive force. These properties resembled those of soft ferromagnetic materials. The ferromagnetic behavior was indicated even at 800 K. Polymers of o-and p-phenylenediamines exhibited lower values of saturation magnetization than polymers of m-phenylenediamine.
๐ SIMILAR VOLUMES
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. T
M. B
In this report, we describe the use of in situ NMR spectroscopy to elucidate the mechanism of horseradish peroxidase-catalyzed oxidative free-radical coupling of phenols. We demonstrate the potential of the technique for the polymerization of 8-hydroxyquinoline-5-sulfonate (HQS). Based on the struct