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Aqueous Solutions of Mo-V-Phosphoric Heteropoly Acids as Bifunctional Catalysts for Preparation of 9,10-Anthraquinone and Its Hydrogenated Derivatives Full article

Journal ChemCatChem
ISSN: 1867-3880 , E-ISSN: 1867-3899
Output data Year: 2012, Volume: 4, Number: 9, Pages: 1405-1410 Pages count : 6 DOI: 10.1002/cctc.201200039
Tags Cycloaddition, Homogeneous catalysis, Molybdenum, Quinones, Vanadium
Authors Zhizhina Elena G. 1 , Odyakov Viktor F. 1
Affiliations
1 Department of Catalytic Processes of Fine Organic Synthesis Boreskov Institute of Catalysis Siberian Branch of Russian Academy of Sciences Prospekt Akademika Lavrentieva 5, Novosibirsk 630090 (Russia)

Abstract: Acid-catalyzed condensation of 1,3-butadiene with para-quinones and oxidation of resulting adducts can be performed as an one-pot process in the presence of aqueous solutions of Мо-V-P heteropoly acids (HPA) having the general HaPzMoyVxOb composition. The solutions have bifunctional catalytic properties, i.e. they are strong Brönsted acids and reversible oxidants. By condensation of hydroquinone, 1,4-benzoquinone, or 1,4-naphthoquinone with 1,3-butadiene in the HPA solutions, 9,10-anthraquinone (AQ) is prepared in the mixture with tetrahydro-AQ (THA) and dihydro-AQ (DHA). In the course of this one-pot process proceeding without organic solvents, the HPA solution is reduced. A slight soluble mixture of THA, DHA, and AQ almost quantitatively is precipitated and filtered off. The non-Keggin-type Н12P3Mo18V7O85 solution has the highest productivity in this process. This solution can be rapidly regenerated by dioxygen or air at temperatures up to 170С and then reused. The prepared (THA + DHA + AQ) mixture can be successfully used as a catalyst for alkaline delignification of wood. Our homogeneous bifunctional HPA catalyst is very stable and promising for use in similar one-pot processes.
Cite: Zhizhina E.G. , Odyakov V.F.
Aqueous Solutions of Mo-V-Phosphoric Heteropoly Acids as Bifunctional Catalysts for Preparation of 9,10-Anthraquinone and Its Hydrogenated Derivatives
ChemCatChem. 2012. V.4. N9. P.1405-1410. DOI: 10.1002/cctc.201200039 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jan 20, 2012
Accepted: Mar 14, 2012
Published online: Jun 8, 2012
Published print: Sep 1, 2012
Identifiers:
Web of science: WOS:000308037400026
Scopus: 2-s2.0-84865612173
Elibrary: 20473029
Chemical Abstracts: 2012:829344
Chemical Abstracts (print): 158:216353
OpenAlex: W2084178216
Citing:
DB Citing
Web of science 20
Scopus 21
Elibrary 25
OpenAlex 22
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