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Study of biologically active solid-phase systems based on halogen-substituted nitrobenzofuroxans by the ir spectroscopy method

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dc.contributor.author Khuziakhmetova A.N.
dc.contributor.author Gorelova E.G.
dc.contributor.author Yusupova L.M.
dc.contributor.author Kurmaeva A.A.
dc.date.accessioned 2021-02-25T21:01:09Z
dc.date.available 2021-02-25T21:01:09Z
dc.date.issued 2020
dc.identifier.issn 2305-2066
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/162892
dc.description.abstract © Khuziakhmetova A. N., Gorelova E. G., Yusupova L. M., Kurmaeva A. A., 2020. Introduction. Biologically active compounds 4,6-dinitro-5,7-dichlorobenzofuroxan (4,6-DNDHBFO) and 5-nitro-4,6-dichlorobenzofuroxan (5-NDHBFO) effectively in-hibit ultra-resistant microorganisms: Staphylococcus aureus, pathogenic fungi – Aspergillius niger, Coniophora cerebella, Candida albicanas and other microor-ganisms. Mixed systems based on 4,6-DNDHBFO and 5-NDHBFO exhibit high potentiated synergistic activity against Aspergillius niger. Currently, there are no full-fledged studies about the mechanism of synergism of 5-NDHBFO and 4,6-DNDHBFO in a solid-phase system. The results of the study of solid-phase sys-tems 5-NDHBFO – 4,6-DNDHBFO by IR spectroscopy will make it possible to establish the nature of the interaction between the components of the binary mix-ture. Aim. Experimental study of the intermolecular interaction of 5-NDHBFO with 4,6-DNDHBFO by the IR spectroscopy method. Materials and methods. The intermolecular interaction of 5-NDHBFO with 4,6-DNDHBFO at different ratios in a solid-phase system was studied by the IR spectroscopy method. Results and discussion. Based on the results of the study, the physico-chemical interaction of 5-NDHBPO with 4,6-DNDHBFO in solid-phase systems was revealed. Shifts and changes in the intensities of the characteristic frequencies of functional groups involved in the formation of intermolecular bonds between 5-NDHBPO and 4,6-DNDHBPO were revealed. Conclusion. The nature of the interaction between 4,6-DNDHBFO and 5-NDHBFO in the solid-phase system was established, leading to the appearance of a synergy effect. The interaction of 5-NDHBFO with 4,6-DNDHBFO in a bi-nary system is due to the formation of an intermolecular hydrogen bond. The in-teraction involves the proton of the 5-NDHBFO molecule, the oxygen of the fu-roxan ring of 4,6-DNDHBFO, as well as the halogen atom of 4,6-DNDHBFO at an equimolar ratio of the components of the solid-phase system.
dc.relation.ispartofseries Drug Development and Registration
dc.subject 4,6-dinitro-5,7-dichlorobenzofuroxan
dc.subject 5-nitro-4,6-dichlorobenzofuroxan
dc.subject Binary solid-phase systems
dc.subject Intermolecular hydrogen bond
dc.subject IR spec-troscopy method
dc.subject Synergistic effect
dc.title Study of biologically active solid-phase systems based on halogen-substituted nitrobenzofuroxans by the ir spectroscopy method
dc.type Article
dc.relation.ispartofseries-issue 4
dc.relation.ispartofseries-volume 9
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 32
dc.source.id SCOPUS23052066-2020-9-4-SID85097266238


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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