ملخص
The reduction of VO(η2-O2)(pyridine-2-carboxylate) by Fe(H2O)6 2+ proceeds via formation of the transient complex (pyridine-2-carboxylate)(O)VV(μ-η2: η2-O2)FeII(H2O)3 2+ that is transformed via intramolecular electron transfer into (pyridine-2-carboxylate)(O)VIV(μ-η2: η2-O2)FeIII(H2O)3 2+. The latter transient reacts with another Fe(H2O)6 2+ to yield 2Fe(H2O)6 3+ + VVO(OH)(pyridine-2-carboxylate)+. These results point out that: (1) VV does not activate the η2 bound peroxide toward the Fenton-like reaction. In this aspect, VV differs from FeIII in (H2O)5Fe–OOH2+ and (2) transients of the type LmMn(μ-η2: η2-O2)M′L″l have to be considered in the reductions of complexes of η2-bound peroxides.
اللغة الأصلية | الإنجليزيّة |
---|---|
الصفحات (من إلى) | 1722-1729 |
عدد الصفحات | 8 |
دورية | Journal of Coordination Chemistry |
مستوى الصوت | 69 |
رقم الإصدار | 11-13 |
المعرِّفات الرقمية للأشياء | |
حالة النشر | نُشِر - 2 يوليو 2016 |