Pathways of 1O2, transfer in the oxidation of anthracenes with the H2O2/VV/AcOH system

被引:9
作者
Gekhman, AE
Amelichkina, GE
Moiseeva, NI
Vargaftik, MN
Moiseev, II
机构
[1] Russian Acad Sci, NS Kurnakov Gen & Inorgan Chem Inst, Moscow 117907, Russia
[2] Russian Acad Sci, NN Semenov Chem Phys Inst, Moscow 117977, Russia
基金
俄罗斯基础研究基金会;
关键词
hydrogen peroxide decomposition; homogeneous catalysis; singlet dioxygen formation; vanadium(V) complexes; kinetic of anthracenes oxidation; singlet dioxygen transfer to substrate molecule;
D O I
10.1016/S1381-1169(00)00325-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Anthracene and its alkyl derivatives were found to undergo oxidation by the V-V/H2O2/AcOH catalytic system via a polar mechanism involving the transfer of singlet dioxygen from the vanadium(V)/O-I(2) exniplex to the molecule of unsaturated substrate. The free singlet dioxygen O-1(2)((1)Delta (g)) molecule is practically inactive toward anthracene in the AcOH solution. The vanadium(V) complex with the singlet dioxygen ligand was suggested to be the only oxidant species active in the reaction. The deactivation rate of the complex is similar to 1.5 times less than the rate of its reaction with 2-ethylanthracene (10(-2) M). Meantime, the analogous ratio of the O-1(2) dissolved in AcOH solution is similar to 15 at the same 2-ethylanthracene concentration. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:111 / 124
页数:14
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