The Role of Water-Based Hydrogen Atom Wires in Long-Range Electron-Transfer Reactions in Aqueous Media for the FeII-FeIIISelf-Exchange and Related Systems

2013 ◽  
Vol 19 (48) ◽  
pp. 16187-16191 ◽  
Author(s):  
Araceli G. Campaña ◽  
Elena Buñuel ◽  
Juan M. Cuerva ◽  
Diego J. Cárdenas
Keyword(s):  
Electron Transfer ◽  
Hydrogen Atom ◽  
Long Range ◽  
Aqueous Media ◽  
Transfer Reactions ◽  
Electron Transfer Reactions ◽  
Water Based

Electron-transfer reactions in non-aqueous media. VII. Reduction of CoF(NH3)52+ and Co(HCOO)(NH3)52+ by copper(I) in dimethyl sulfoxide-water mixtures

1983 ◽  
Vol 36 (10) ◽  
pp. 1923 ◽  
Author(s):  
JMB Harrowfield ◽  
L Spiccia ◽  
DW Watts
Keyword(s):  
Electron Transfer ◽  
Dimethyl Sulfoxide ◽  
Aqueous Media ◽  
Mixed Solvents ◽  
Transfer Reactions ◽  
Aprotic Solvents ◽  
Aqueous Mixtures ◽  
Electron Transfer Reactions ◽  
Dipolar Aprotic Solvents ◽  
Sphere Mechanism

Previous work on the reduction of a series of cobalt(III) complexes by iron(II) in dipolar aprotic solvents and in aqueous mixtures has been extended to reduction by copper(I). The greater stability of copper(I) to disproportionation in these media has permitted the study of the reduction of CoF(NH3)52+ and Co(HCOO)(NH3)52+ in range of solvents over a number of temperatures with a precision not possible in previous studies in water. The results are consistent with an inner-sphere mechanism in which the copper(I) reductant is preferentially solvated by dimethyl sulfoxide to the exclusion of water in mixed solvents.

2-Hydroxyphenyl-1,3-dimethylbenzimidazolines. Formal Two Hydrogen Atom-donors for Photoinduced Electron Transfer Reactions

2004 ◽  
Vol 33 (1) ◽  
pp. 18-19 ◽  
Author(s):  
Eietsu Hasegawa ◽  
Naoki Chiba ◽  
Tomoya Takahashi ◽  
Shinya Takizawa ◽  
Takashi Kitayama ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Hydrogen Atom ◽  
Photoinduced Electron Transfer ◽  
Transfer Reactions ◽  
Electron Transfer Reactions

Electron-transfer reactions in non-aqueous media. II. Reduction of CoF(NH3)52+, CoCl(NH3)52+ and CoBr(NH3)52+ by iron(II) in dimethyl sulphoxide-water mixtures

1976 ◽  
Vol 29 (1) ◽  
pp. 97 ◽  
Author(s):  
BA Matthews ◽  
DW Watts
Keyword(s):  
Electron Transfer ◽  
Aqueous Media ◽  
Activation Parameters ◽  
Solvent Composition ◽  
Dimethyl Sulphoxide ◽  
Transfer Reactions ◽  
Octahedral Coordination ◽  
Electron Transfer Reactions ◽  
Kinetics Of

The kinetics of the reduction of the cobalt(111) octahedral complexes, CoF(NH3)52+, CoCl(NH3)52+ and CoBr(NH3)52+, by iron((11) in various Me2SO-H2O mixtures have been studied over a range of temperatures. The activation parameters obtained for the chloro and bromo systems are consistent with a change in the stereochemistry of the iron (11) atom in the bridged intermediate from octahedral in water to tetrahedral with increasing Me2SO concentration. The fluoro system, however, has activation parameters which are less sensitive to solvent composition and consistent with the iron(11) atom maintaining octahedral coordination.

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