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Vanadium-substituted polyoxomolybdate

Also, the vanadium-substituted polyoxomolybdate, Q5[PV2Moio04o] (see Figure 9.1b, Q = (C4Hg)4N ) was catalytically active and highly selective in the oxidation of primary and secondary alcohols with nitrous oxide to yield aldehydes and ketones, respectively. Scheme 9.3 [25]. In addition, the same catalyst under similar conditions catalyzed the oxidation of alkylarenes. Scheme 9.3. In the oxidation of alkylarenes with hydrogen atoms at P positions, the substrate is dehydrogenated, for example, cumene to a-methylstyrene, whereas in the absence of p hydrogen atoms ketones are formed, for example, diphenylmethane to benzophenone. [Pg.321]

Also the vanadium substituted polyoxomolybdate, " Q5[PV2Moio04o], [see Figure 1(b), = (C4H9)4N ], was catalyticaUy active and highly selective in the oxidation of... [Pg.181]

Catalytic Tetrahydropyranylation of Phenols and Alcohols Using Vanadium(V)-Substituted Polyoxomolybdates... [Pg.97]

Gharib A, Jahangir M (2012) Catalytie tetrahydropyranylation of phenols and alcohols using vanadium(V)-substituted polyoxomolybdates. J Serb Chem Soc 77 287-296... [Pg.104]


See other pages where Vanadium-substituted polyoxomolybdate is mentioned: [Pg.92]    [Pg.70]    [Pg.310]   
See also in sourсe #XX -- [ Pg.321 ]




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Polyoxomolybdate

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