Kinetics and Thermodynamics of Formation and Electron‐Transfer Reactions of Surfactant Cobalt(III) Complexes Containing Polypyridyl Ligands with Fe(CN)64− in Microheterogeneous Environment. Issue 3 (16th January 2015)
- Record Type:
- Journal Article
- Title:
- Kinetics and Thermodynamics of Formation and Electron‐Transfer Reactions of Surfactant Cobalt(III) Complexes Containing Polypyridyl Ligands with Fe(CN)64− in Microheterogeneous Environment. Issue 3 (16th January 2015)
- Main Title:
- Kinetics and Thermodynamics of Formation and Electron‐Transfer Reactions of Surfactant Cobalt(III) Complexes Containing Polypyridyl Ligands with Fe(CN)64− in Microheterogeneous Environment
- Authors:
- Nagaraj, Karuppiah
Murugan, Krishnan Senthil
Thangamuniyandi, Pilavadi
Sakthinathan, Subramanian - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <p>The electron‐transfer reaction of some surfactant cobalt(III) complexes, <italic>cis</italic>‐[Co(ip)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>1</bold>, <italic>cis</italic>‐[Co(dpq)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>2</bold>, and <italic>cis</italic>‐[Co(dpqc)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>3</bold> (ip = imidazo[4, 5‐f][1, 10]phenanthroline, dpq = dipyrido[3, 2‐d:2′‐3′‐f]quinoxaline, dpqc = dipyrido[3, 2‐a:2′, 4′‐c](6, 7, 8, 9‐tetrahydro)phenazine, C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub> = dodecylamine) with the Fe(CN)<sub>6</sub><sup>4−</sup> ion has been investigated in microheterogeneous media (micelles, β‐cyclodextrin) at different temperatures by the spectrophotometric method under pseudo‐first‐order conditions using an excess of the reductant. Experimentally, the reaction was found to be second order and the electron transfer postulated as an outer sphere. The rate constant for the electron‐transfer reaction in micelles was found to increase with an increase in the initial concentration of the surfactant–cobalt(III) complex. This peculiar behavior of dependence of the second‐order rate constant on the initial concentration of one of the reactants has been attributed to the presence of various concentrations of micelles under different<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <p>The electron‐transfer reaction of some surfactant cobalt(III) complexes, <italic>cis</italic>‐[Co(ip)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>1</bold>, <italic>cis</italic>‐[Co(dpq)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>2</bold>, and <italic>cis</italic>‐[Co(dpqc)<sub>2</sub>(C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub>)<sub>2</sub>]<sup>3+</sup><bold>3</bold> (ip = imidazo[4, 5‐f][1, 10]phenanthroline, dpq = dipyrido[3, 2‐d:2′‐3′‐f]quinoxaline, dpqc = dipyrido[3, 2‐a:2′, 4′‐c](6, 7, 8, 9‐tetrahydro)phenazine, C<sub>12</sub>H<sub>25</sub>NH<sub>2</sub> = dodecylamine) with the Fe(CN)<sub>6</sub><sup>4−</sup> ion has been investigated in microheterogeneous media (micelles, β‐cyclodextrin) at different temperatures by the spectrophotometric method under pseudo‐first‐order conditions using an excess of the reductant. Experimentally, the reaction was found to be second order and the electron transfer postulated as an outer sphere. The rate constant for the electron‐transfer reaction in micelles was found to increase with an increase in the initial concentration of the surfactant–cobalt(III) complex. This peculiar behavior of dependence of the second‐order rate constant on the initial concentration of one of the reactants has been attributed to the presence of various concentrations of micelles under different initial concentrations of the surfactant–cobalt(III) complex in the reaction medium. Inclusion of the long aliphatic chain of the surfactant complex ion into β‐cyclodextrin leads to decrease in the rate constant. Kinetic data and activation parameters are interpreted in terms of an outer‐sphere electron‐transfer mechanism. All these results have been interpreted in terms of the hydrophobic effect and the reactants with the opposite charge.</p> </abstract> … (more)
- Is Part Of:
- International journal of chemical kinetics. Volume 47:Issue 3(2015:Mar.)
- Journal:
- International journal of chemical kinetics
- Issue:
- Volume 47:Issue 3(2015:Mar.)
- Issue Display:
- Volume 47, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 47
- Issue:
- 3
- Issue Sort Value:
- 2015-0047-0003-0000
- Page Start:
- 174
- Page End:
- 182
- Publication Date:
- 2015-01-16
- Subjects:
- Chemical kinetics -- Periodicals
541.394 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4601 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/kin.20901 ↗
- Languages:
- English
- ISSNs:
- 0538-8066
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.165000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3423.xml