Photosensitized electron-transfer reactions in .beta.-cyclodextrin aqueous media: effects on dissociation of ground-state complexes, charge separation, and hydrogen evolution

1986 ◽  
Vol 108 (16) ◽  
pp. 4696-4700 ◽  
Author(s):  
Eti. Adar ◽  
Yinon. Degani ◽  
Zafrir. Goren ◽  
Itamar. Willner
1983 ◽  
Vol 36 (10) ◽  
pp. 1923 ◽  
Author(s):  
JMB Harrowfield ◽  
L Spiccia ◽  
DW Watts

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.


1978 ◽  
Vol 82 (17) ◽  
pp. 1879-1885 ◽  
Author(s):  
D. Meyerstein ◽  
J. Rabani ◽  
M. S. Matheson ◽  
D. Meisel

2019 ◽  
Vol 55 (8) ◽  
pp. 1176-1176
Author(s):  
Elin Sundin ◽  
Maria Abrahamsson

Correction for ‘Long-lived charge separation in dye–semiconductor assemblies: a pathway to multi-electron transfer reactions’ by Elin Sundin et al., Chem. Commun., 2018, 54, 5289–5298.


1976 ◽  
Vol 29 (1) ◽  
pp. 97 ◽  
Author(s):  
BA Matthews ◽  
DW Watts

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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