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Oxidative polymerization of phenylenediamines in reversed micelles

✍ Scribed by Daigo Ichinohe; Norihiro Saitoh; Hideo Kise


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
480 KB
Volume
199
Category
Article
ISSN
1022-1352

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πŸ“œ SIMILAR VOLUMES


Oxidative polymerization of phenylenedia
✍ Daigo Ichinohe; Toshitaka Muranaka; Toshiya Sasaki; Masami Kobayashi; Hideo Kise πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 169 KB πŸ‘ 2 views

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 phenylenedia
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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

Deactivation and conformational changes
✍ E. P. Melo; C. M. L. Carvalho; M. R. Aires-Barros; S. M. B. Costa; J. M. S. Cabr πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 75 KB πŸ‘ 1 views

Deactivation data and fluorescence intensity changes were used to probe functional and structural stability of cutinase in reverse micelles. A fast deactivation of cutinase in anionic (AOT) reverse micelles occurs due to a reversible denaturation process. The deactivation and denaturation of cutinas