57701-98-1Relevant articles and documents
Hydroxyl-radical-induced Oxidation of Cyclohexa-1,4-diene by O2 in Aqueous Solution. A Pulse Radiolysis and Product Study
Pan, Xian-Ming,Schuchmann, Man Nien,Sonntag, Clemens von
, p. 1021 - 1028 (2007/10/02)
Hydroxyl radicals have been generated radiolytically in N2O/O2 (4 : 1)-saturated aqueous solutions.They react with cyclohexa-1,4-diene by H-abstraction and by addition to a double bond yielding equal amounts of cyclohexadienyl 1 and 6-hydroxycyclohex-3-enyl radicals 2.As shown by pulse radiolysis, 1 and 2 react with O2 with an overall rate constant of k = 1.2 * 109 dm3 mol-1s-1.Radical 1 yields two isomeric peroxyl radicals: 4(cyclohexa-1,3-diene structure) and 5(cyclohexa-1,4-diene structure).Since the C-H ... radical-O-O distance in 4 is only ca. 1.8 Angstroem, it is suggested that 4 is the radical which rapidly eliminates HO2(radical) (k 8 * 105 s-1 as measured by pulse radiolysis) yielding benzene (ca. 60percent of 4 + 5).The peroxyl radical 5 which has a longer C-H ...radical-O-O distance (ca. 3.8 Aongstrem) might not undergo this reaction.Instead it undergoes intramolecular cyclization thereby forming endoperoxidic intermediates which are believed to be the precursors of products which upon reduction with NaBH4 yield trihydroxycyclohexenes.In the presence of superoxide dismutase to remove O2(anion) radicals and at low cyclohexa-1,4-diene concentration (4 * 10-4 mol dm-3), the 6-hydroxycyclohex-3-en-yl-peroxyl radicals 6 and 7 derived from 2 decay bimolecularly yielding equal amounts of 4,5-dihydroxycyclohexene, 6-hydroxycyclohex-3-enone and oxygen (k = 1.3 * 108 dm3 mol-1 s-1).At high cyclohexa-1,4-diene concentration (10-2 mol dm-3) 6 and 7 abstract H-atoms from the substrate (k = 820 dm3 mol-1 s-1) yielding the corresponding 6-hydroxycyclohex-3-enyl hydroperoxides.In competition with these bimolecular reactions, 6 and 7 also undergo intramolecular cyclization similar to radical 5.In subsequent reactions endoperoxidic products are formed which have been identified as tetrahydroxycyclohexanes after reduction with NaBH4.A number of fragment products with one to three carbon atoms have also been found which may result from the degradation of some of the endoperoxidic intermediates derived from the radicals 5, 6 and 7.A material balance is presented which accounts for the oxygen consumed in this system.
The Strength of the R-O2. Bond in Peroxy-radicals and the Reversibility of the Reaction R. + O2 ->/.
Finkel'shtein, E. I.,Gerasimov, G. N.
, p. 570 - 572 (2007/10/02)
An equation is proposed for the calculation of the R-O2. bond strength in peroxy-radicals: DR-O2. = DR-H - 254.4 kJ mol-1.The calculated equilibrium constants of the reactions R. + O2 ->/-
