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Electron transfer reactions. Reaction of furanones and bifurandiones with potassium and oxygen
Author(s) -
Pandey Bipin,
Tikare Ravindra K.,
Muneer Mohammed,
Kamat Prashant V.,
George Manapurathu V.
Publication year - 1986
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19861190315
Subject(s) - chemistry , benzophenone , potassium , benzoic acid , medicinal chemistry , oxygen , fragmentation (computing) , photochemistry , organic chemistry , computer science , operating system
Treatment of furanones ( 1a – c, 25, 34 ) and bifurandiones ( 23, 37 ) with potassium in THF gave rise to radical anion intermediates, which reacted with oxygen to give superoxide and ultimately products derived through the reaction of superoxide with the starting furanones and bifurandiones. Thus, the reaction of 1a with potassium gave a mixture of 4‐oxo‐2,2,4‐triphenylbutanoic acid ( 7a ), 1,3,3‐triphenyl‐2‐propen‐1‐one ( 11a ), and benzoic acid ( 12 ). The reaction of 11a itself, under similar conditions, gave a mixture of benzophenone ( 18a ) and 12 . Similar reactions have been observed in the case of 1b and c . The bifurandione 23 , on treatment with potassium, gave a mixture of the 2(5 H )‐furanone 25 , 2,3‐diphenylpropenoic acid ( 31 ), and 12 . The reaction of 25 itself with potassium under similar conditions gave the same mixture of 31 and 12 . Treatment of 3‐phenyl‐2(3 H )‐benzofuranone ( 34 ) with potassium, however, did not give any isolable product; only the starting material could be recovered. Under similar conditions, the bifurandione 37 gave the fragmentation product 34 . Cyclic voltammetric studies have been employed to measure the reduction potentials, leading to radical anions, and these intermediates have been characterized through their electronic spectra.