Prospects of Application of Mo–V-Phosphoric Heteropolyacid Solutions as Bifunctional Catalysts for Syntheses of Anthraquinones and Their Substituted Derivatives
Научная публикация
Общее |
Язык:
Английский,
Жанр:
Статья (Full article),
Статус опубликования:
Опубликована,
Оригинальность:
Переводная
|
Журнал |
Russian Chemical Bulletin
ISSN: 1066-5285
, E-ISSN: 1573-9171
|
Вых. Данные |
Год: 2015,
Том: 64,
Номер: 9,
Страницы: 2069-2075
Страниц
: 7
DOI:
10.1007/s11172-015-1119-8
|
Ключевые слова |
anthraquinones, diene synthesis, heteropolyacids |
Авторы |
Gogin L.
1
,
Zhizhina E.G.
1
,
Pai Z.P.
1
,
Parmon V.N.
1,2
|
Организации |
1 |
G. K. Boreskov Institute of Catalysis, Russian Academy of Sciences, 5 prosp. Akad. Lavrent´eva, 630090 Novosibirsk, Russian Federation.
|
2 |
Novosibirsk State University, 2 ul. Pirogova, 630090 Novosibirsk, Russian Federation
|
|
The acid-catalyzed condensation of 1,3-butadienes with p-quinones and oxidation of the obtained adducts can be carried out as one-pot process in the presence of aqueous solutions of Mo–V–P-heteropolyacids (HPA) of the general composition HaPzMoyVxOb. These solutions act as bifunctional catalysts, since they simultaneously behave as strong Brönsted acids and fairly strong reversible oxidants. The condensation of 1,4-naphthoquinone (NQ) with 1,3-butadiene in solutions of high-vanadium HPA of the empirical compositions H15P4Mo18V7O89 and H17P3Mo16V10O89 in the presence of water-miscible organic solvents (acetone, 1,4-dioxane) affords 9,10-anthraquinone in a yield of ~70% and purity up to 97% at a complete conversion of NQ. Under similar conditions, the reactions of NQ and substituted 1,3-butadienes afford substituted anthraquinones in the yields up to 90% and purity up to 99%. The catalysts are regenerated with oxygen in an individual step and can be reused.