CATALYSIS BY TOPOLOGICALLY ANCHORED METAL-COMPLEXES - LIQUID-PHASE HYDROXYLATION OF BENZENE BY H2O2 IN THE PRESENCE OF ZEOLITE-SUPPORTED FE(II) PHTHALOCYANINE
Ns. Zefirov et An. Zakharov, CATALYSIS BY TOPOLOGICALLY ANCHORED METAL-COMPLEXES - LIQUID-PHASE HYDROXYLATION OF BENZENE BY H2O2 IN THE PRESENCE OF ZEOLITE-SUPPORTED FE(II) PHTHALOCYANINE, Canadian journal of chemistry, 76(6), 1998, pp. 955-959
Fe(LI) phthalocyanine topologically anchored on NaA zeolite has been p
repared. The catalytic activity of zeolite-supported Fe(II) phthalocya
nine has been studied in the liquid-phase hydroxylation of benzene by
H2O2. The main product of the reaction at room temperature is phenol.
By refluxing, the reaction proceeds to give the products of subsequent
oxidation, i.e., hydroquinone and p-benzoquinone, in low yields.