Aerobic Oxidations of Conjugated Dienes Using a Catalytic Palladium(II)−Quinone−Heteropolyacid System for Electron Transfer from Organic Substrates to Molecular Oxygen

1998 ◽  
Vol 17 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Katarina Bergstad ◽  
Helena Grennberg ◽  
Jan-E. Bäckvall
RSC Advances ◽  
2021 ◽  
Vol 11 (35) ◽  
pp. 21359-21366
Author(s):  
Debabrata Chatterjee ◽  
Marta Chrzanowska ◽  
Anna Katafias ◽  
Maria Oszajca ◽  
Rudi van Eldik

[RuII(edta)(L)]2–, where edta4– =ethylenediaminetetraacetate; L = pyrazine (pz) and H2O, can reduce molecular oxygen sequentially to hydrogen peroxide and further to water by involving both outer-sphere and inner-sphere electron transfer processes.


2015 ◽  
Vol 68 (11) ◽  
pp. 1640 ◽  
Author(s):  
Eietsu Hasegawa ◽  
Shin-ya Takizawa

2-Aryl-1,3-dimethylbenzimidazolines (DMBIHs) have been applied to photoinduced electron-transfer reductions of various organic substrates. Either direct or indirect electron transfer between the substrates and DMBIHs is utilized to promote the desired transformations. Photoexcitation of the substrates using light above 280 nm was carried out in the former protocol whereas a photosensitization method using materials such as substituted pyrenes, ruthenium and iridium complexes that absorb longer-wavelength light was employed in the latter. In these reactions, DMBIHs undergo initial electron transfer and subsequent proton or hydrogen atom transfer.


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