## Abstract Using the analysis of the splitting constants of the ESR spectra, factor are described which affect the stability of free phenoxyls and of phenoxyls co‐ordinated on cobalt, generated by the reaction of __tert__‐butyleperoxyls and 4,4′‐biphenyldiols (1), 4,4′–thiobisphenols (2 and 5), 4,
Enzymatic synthesis of a soluble polyphenol derivative from 4,4′-biphenyldiol
✍ Scribed by Shiro Kobayashi; Hideharu Kurioka; Hiroshi Uyama
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 295 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
Enzymatic oxidative polymerization of 4,4′‐biphenyldiol was performed in an aqueous organic solvent using horseradish peroxidase as catalyst. In the polymerization using a mixture of 1,4‐dioxane and phosphate buffer (pH 7.0) (80:20 vol‐%) as solvent, the monomer was quantitatively consumed to give powdery polymeric materials in a high yield. The resulting polymer is soluble in polar solvents such as N,N‐dimethylformamide, dimethyl sulfoxide, and acetone. The molecular weight of the methylated product is 7.3 × 10^3^. The polymer exhibits high thermal stability under nitrogen.
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New aromatic diamines [(1) and ( 2)] containing polycycloalkane structures between two benzene rings were synthesized by HCl-catalyzed condensation reaction of aniline hydrochloride and corresponding polycycloalkanone derivatives. The structures of diamines were identified by 1 H-NMR, 13 C-NMR, FTIR
UV-Vis spectra of 6F-HAB-ETPVP polymer films exposed to unpolarized UV light (260 -380 nm) at varying exposure dose.
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