Форма представления | Статьи в зарубежных журналах и сборниках |
Год публикации | 2019 |
Язык | английский |
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Ямбушев Фарид Джамалетдинович, автор
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Библиографическое описание на языке оригинала |
Yambyshev, F.D. Synthesis method and investigation of O-, M-, p-nitrophenylarsonic acid properties // Journal of Computational and Theoretical Nanoscience. - 2019, V.16, Is.11.- P. 4481-4485 |
Аннотация |
Journal of Computational and Theoretical Nanoscience |
Ключевые слова |
Arsenization; Arylarsonic Acid; Derivatives of Arsenic; Diazotization; Phenylarsonic Acid |
Название журнала |
Journal of Computational and Theoretical Nanoscience
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URL |
https://www.researchgate.net/publication/338212556_Synthesis_Method_and_Investigation_of_o-_m-_p-Nitrophenylarsonic_Acid_Properties |
Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на эту карточку |
https://repository.kpfu.ru/?p_id=283524 |
Полная запись метаданных |
Поле DC |
Значение |
Язык |
dc.contributor.author |
Ямбушев Фарид Джамалетдинович |
ru_RU |
dc.date.accessioned |
2019-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2019-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2019 |
ru_RU |
dc.identifier.citation |
Yambyshev, F.D. Synthesis method and investigation of O-, M-, p-nitrophenylarsonic acid properties // Journal of Computational and Theoretical Nanoscience. - 2019, V.16, Is.11.- P. 4481-4485 |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/?p_id=283524 |
ru_RU |
dc.description.abstract |
Journal of Computational and Theoretical Nanoscience |
ru_RU |
dc.description.abstract |
The importance of studying arylated arsenic derivatives is conditioned by a number of reasons. In particular, as biologically active substances, they attract attention in terms of their fungicidal activity and stimulating effect on cardiac activity. Besides, they serve as an interesting object for intermolecular interaction study conditioned by the H-bond. Finally, as the main starting products, they are the source of a wide range of arsenic-organic compound synthesis, including aromatic primary, secondary arsinghalides, tertiary asymmetric arsines and their derivatives. The aim of the present work was to study the possibility of diazonium salt use obtained from weakly basic arylamines in a strongly acidic medium for arylation of arsinic acid sodium salt. This article discusses the methods for the synthesis of arylated arsenic derivatives containing the substituents in the benzene ring that affect the electronic structure, reactivity, and biological properties of the compounds. They studied the ability of an arsenic atom to transit from a four-coordinate state to a five-coordinate state with the formation of strong monohydrates. They showed the disadvantages and positive aspects of the already known and used synthesis methods. The most practical version of arylated arsenic compound synthesis has been tested and recommended. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
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ru_RU |
dc.title |
Synthesis method and investigation of O-, M-, p-nitrophenylarsonic acid properties |
ru_RU |
dc.type |
Статьи в зарубежных журналах и сборниках |
ru_RU |
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