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Oxidation, Oxidative Esterification and Ammoxidation of Acrolein over Metal Oxides: Do These Reactions Include Nucleophilic Acyl Substitution? Научная публикация

Конференция 11th European Workshop on Selective Oxidation - Selectivity in Oxidation - Key to New Resources Valorization (ISO) during the 12th European Congress on Catalysis - Balancing the Use of Fossil and Renewable Resources (Europacat)
30 авг. - 4 сент. 2015 , Kazan
Журнал Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Вых. Данные Год: 2017, Том: 279, Страницы: 90-94 Страниц : 5 DOI: 10.1016/j.cattod.2015.12.030
Ключевые слова Acrolein, Acrylic acid, Acrylonitrile, Methyl acrylate, Nucleophilic acyl substitution, Vanadium mixed oxide catalyst
Авторы Koltunov Konstantin Yu. 1,2 , Sobolev Vladimir I. 1,3 , Bondareva Valentina M. 1
Организации
1 Boreskov Institute of Catalysis, Russian Academy of Sciences, Pr. Akademika Lavrentieva, 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova, 2, Novosibirsk 630090, Russia
3 Tomsk State University, 36 Lenina Ave., Tomsk 634050, Russia

Информация о финансировании (1)

1 Федеральное агентство научных организаций России V.44.2.7.

Реферат: It is known that nucleophilic acyl substitution in the RCOX compounds with “good leaving” groups X is a fundamental and energetically favorable route to carboxylic acid derivatives. When water, alcohols and ammonia are used as nucleophiles, carboxylic acids, esters and amides (or nitriles) are obtained, respectively. On the other hand, the same products are derived from aldehydes upon their catalytic aerobic oxidation, on condition that water, alcohols and ammonia are present in the feed gas. Therefore, one can surmise that nucleophilic substitution reactions are involved intrinsically in the catalytic oxidation reactions. In agreement with this hypothesis we have shown, as an example, that the selfsame catalyst, MoVTeNb mixed oxides, enables successful oxidation, oxidative esterification and ammoxidation of acrolein. The mechanistic aspects of these reactions are considered based on established organic and general chemistry principles.
Библиографическая ссылка: Koltunov K.Y. , Sobolev V.I. , Bondareva V.M.
Oxidation, Oxidative Esterification and Ammoxidation of Acrolein over Metal Oxides: Do These Reactions Include Nucleophilic Acyl Substitution?
Catalysis Today. 2017. V.279. P.90-94. DOI: 10.1016/j.cattod.2015.12.030 WOS Scopus РИНЦ OpenAlex CAPlus
Даты:
Поступила в редакцию: 5 окт. 2015 г.
Принята к публикации: 17 дек. 2015 г.
Опубликована online: 11 февр. 2016 г.
Опубликована в печати: 1 янв. 2017 г.
Идентификаторы БД:
≡ Web of science: WOS:000388778100013
≡ Scopus: 2-s2.0-84993138288
≡ РИНЦ: 28222838
≡ OpenAlex: W2254786750
≡ Chemical Abstracts: 2016:234354
Цитирование в БД:
≡ Web of science 13 Сбор данных от 13.02.2026
≡ Scopus 15 Сбор данных от 15.02.2026
≡ РИНЦ 14 Сбор данных от 08.02.2026
≡ OpenAlex 16 Сбор данных от 15.02.2026
Альметрики: