It has been evidenced that microcrystalline chitosan (MCCh) with a determined (by the potentiometric method in nonaqueous medium) degree of deacetylation of 0.87 acts as a polymeric chelating agent with cobalt(I1) and zinc(I1). The predomination of hydrolytic reactions, in the case of copper(I1) ion
Redox reactions of peroxo terpyridine complexes of Cu(II), Zn(II), and Cu(II)Zn(II): A pulse radiolysis study
β Scribed by Sudhir Kapoor; M. S. Sastry
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 123 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
β¦ Synopsis
The reactions of e aq Οͺ , CH 2 OHβ , (CH 3 ) 2 COHβ , O H β and N 3 β radicals with peroxo ΨΟͺ CO , 2 terpyridine complexes of Cu(II), Zn(II), and Cu(II)-Zn(II) in aqueous solution were investigated by pulse radiolysis. The primary products from the reduction and oxidation of the macrocyclic complexes were assigned a radical nature by comparing their optical spectra with those of Cu(I), Zn(I), and Cu(III) species. Such metal-ligand radical products undergo disproportionation that does not lead to the formation of Cu(0) or colloidal copper.
π SIMILAR VOLUMES
In this work the influence of the porphyrin structure and of the nature of the mobile phase upon retention parameters is examined by means of reversed phase high-performance liquid chromatography (HPLC). Acetonitrileβethyl acetate and other mixtures were used as eluents. An increase in the retention
Poly(propylene imine) dendrimers having 8, 32, and 64 primary amine end groups form diamino Cu(II), diamino Zn(II), and tetramino Co(III) complexes that are identified spectrophotometrically and titrimetrically. The dendrimer-metal ion complexes catalyze the hydrolysis of p-nitrophenyl diphenyl phos