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Kinetic studies of a catalyzed metalloporphyrin formation

✍ 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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✦ 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.


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Kinetic studies of liquid-phase acetal f
✍ Satoshi Sato; Keisuke Sagara; Hiromi Furuta; Fumio Nozaki πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 753 KB

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