Kinetic studies of a catalyzed metalloporphyrin formation
β Scribed by Adegboye O. Adeyemo; M. Krishnamurthy
- Book ID
- 102445287
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 382 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Kinetics of the incorporation of mercury(I1) ion in tetra (p-trimethylammonium-pheny1)porphine have been investigated in aqueous solution at 30.0"C and 0.2 M (NaN03) ionic strength. The reaction was found to be first order each in mercury(I1) and the porphyrin. The forward (formation) and the reverse (dissociation) rate constants were found to be 1.9 ? 0.2 x lo3 M-'s-' and 7 ? 2 x lo6 M-'s-', respectively. Kinetics of zincflI) incorporation in tetra(p-trimethylammoniumpheny1)porphine catalyzed by mercury(I1) were also investigated. This catalysis is explained in terms of steady-state formation of mono mercury(II) porphyrin followed by zinc(II) displacement of mercury(I1) ion from the porphyrin. Such a mechanism also illustrates the importance of porphyrin core deformation to metal incorporation.
π SIMILAR VOLUMES
Various acetal formation reactions were examined by a Keggin-type heteropolyacid. The reaction kinetics of the acetal formation was also investigated through comparison of heteropolyacids with other acid catalysts in the reaction between cyclohexanone and 1,2-butandiol to produce cyclohexanone ethyl