In aqueous solution, bis(nucleoside) complexes formed by the reaction of cis-[Pt(NH3)2(H2O)2]2+ with an excess of either adenosine (ado) or a mixture of adenosine and guanosine (guo) undergo a slow N7--> N1 linkage isomerisation in the adenine moiety. The isomerisation probably involves the breaking
Kinetics of Fe(II) reduction of cis-halogeno(dodecylamine) bis(ethylenediamine)- cobalt(III) complex ion in aqueous solutions
✍ Scribed by K. Santhakumar; N. Kumaraguru; S. Arunachalam; M. N. Arumugham
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 208 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
Kinetics of reduction of the surfactant complex ions, cis‐chloro/bromo (dodecylamine)bis(ethylenediamine)cobalt(III) by iron(II) in aqueous solution was studied at 303, 308, and 313 K by spectrophotometry method under pseudo‐first‐order conditions, using an excess of the reductant. The second‐order rate constant remains constant below critical micelle concentration (cmc), but increases with cobalt(III) concentration above cmc, and the presence of aggregation of the complex itself alters the reaction rate. The rate of reaction was not affected by the added [H^+^]. Variation of ionic strength (μ) influences the reaction rate. Activation and thermodynamic parameters have been computed. It is suggested that the reaction of Fe^2+^ (aq) with cobalt(III) complex proceeds by the inner‐sphere mechanism. © 2005 Wiley Periodicals, Inc. Int J Chem Kinet 38: 98–105, 2006
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