Synthesis of octasubstituted cobalt phthalocyanines and their redox properties
β Scribed by Keiichi Sakamoto; Eiko Ohno-Okumura
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 63 KB
- Volume
- 03
- Category
- Article
- ISSN
- 1088-4246
No coin nor oath required. For personal study only.
β¦ Synopsis
Octakis(alkoxymethyl) cobalt phthalocyanines with relatively short side chains were synthesized which exhibited no thermotropic liquid crystalline behaviour. The final products as well as the intermediates have been characterized by proton magnetic resonance, infrared and electron spectra and elemental analysis. Cyclic voltammograms were measured for octakis(alkoxymethyl) cobalt phthalocyanines in order to examine their electron transfer properties. The electron transfer properties of octakis (alkoxymethyl) cobalt phthalocyanines depend on the kind and number of substituents and are due to the interaction between the phthalocyanine ring, the central metal which is influenced by the conjugated p electron current of the porphyrazine ring.
π SIMILAR VOLUMES
A series of 4-(polyfluoroalkoxy)phthalonitriles have been prepared in high yield by nucleophilic substitution of the nitro group in 4-nitrophthalonitrile on polyfluoroalkoxy groups at room temperature. These dinitriles have been cyclotetramerized in the presence of cobalt or copper salts into the co
Thermostable polyamideimides with inherent viscosity of 1.02-1.50 dL/g were synthesized from reacting of diamine-terminated aromatic amide prepolymer with various diisocyanate terminated imide prepolymers. The imide prepolymer was prepared by using 4,4'-diphenylmethane diisocyanate to react with 3,3