Non-Marcus Energy Gap Dependence of Back Electron Transfer in Contact Ion Pairs

1994 ◽  
Vol 116 (6) ◽  
pp. 2434-2436 ◽  
Author(s):  
M. Tachiya ◽  
S. Murata



1990 ◽  
Vol 45 (8) ◽  
pp. 1197-1204 ◽  
Author(s):  
H. Bock ◽  
P. Hänel ◽  
H.-F. Herrmann

The radical anion of dimesityltetraketone (ERed, I = -0.40 V) is easily generated in THF by potassium mirror/[2.2.2]-cryptand reduction. Its contact ion pairs with Na⊕, Cs⊕ and Ba⊕⊕ counter cations, prepared in THF solution by single electron transfer from the respective metals, are characterized by their ESR/ENDOR spectra, which exhibit temperature-dependent metal couplings of aNa⊕ = 0.061 mT (190 K), aCs⊕ = 0.021 mT (190 K), and aBa⊕⊕ = 0.145 mT (295 K).



2018 ◽  
Vol 122 (28) ◽  
pp. 15819-15825 ◽  
Author(s):  
Ayan Bhattacharyya ◽  
Soumalya Mukherjee ◽  
Anju Chadha ◽  
Edamana Prasad


ChemInform ◽  
1989 ◽  
Vol 20 (6) ◽  
Author(s):  
H. BOCK ◽  
P. HAENEL ◽  
H.-F. HERRMANN ◽  
H. TOM DIECK


1988 ◽  
Vol 43 (10) ◽  
pp. 1240-1246 ◽  
Author(s):  
Hans Bock ◽  
Peter Hänel ◽  
H.-F Herrmann ◽  
Heindirk torn Dieck

The structurally different radical anions M⊖ of peralkylated 1-sila-2,5-diazacyclopentane-3,4-dithione and of tetrakis(isopropylthio)-p-benzoquinone are generated by reduction with potassium/2.2.2-cryptand under aprotic conditions in THF solution. On addition of Li⊕B(C6H5)4⊖, both form hitherto elusive sulfur-containing contact ion pairs, which are characterized by their ESR/ENDOR spectra.



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