Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на этот ресурс: http://elar.urfu.ru/handle/10995/130588
Полная запись метаданных
Поле DCЗначениеЯзык
dc.contributor.authorAl-Ithawi, W. K. A.en
dc.contributor.authorKhasanov, A. F.en
dc.contributor.authorKovalev, I. S.en
dc.contributor.authorNikonov, I. L.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorPlatonov, V. A.en
dc.contributor.authorSantra, S.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorRanu, B. C.en
dc.date.accessioned2024-04-05T16:26:38Z-
dc.date.available2024-04-05T16:26:38Z-
dc.date.issued2023-
dc.identifier.citationAl-Ithawi, WKA, Khasanov, AF, Kovalev, IS, Nikonov, IL, Kopchuk, DS, Platonov, VA, Santra, S, Zyryanov, GV & Ranu, BC 2023, 'Mechanosynthesis of Diaminobiphenyls-Based Schiff’s Bases as Simple Probes for the Naked-Eye Detection of Cyanide Ion', Chemistry (Switzerland), Том. 5, № 2, стр. 978-986. https://doi.org/10.3390/chemistry5020066harvard_pure
dc.identifier.citationAl-Ithawi, W. K. A., Khasanov, A. F., Kovalev, I. S., Nikonov, I. L., Kopchuk, D. S., Platonov, V. A., Santra, S., Zyryanov, G. V., & Ranu, B. C. (2023). Mechanosynthesis of Diaminobiphenyls-Based Schiff’s Bases as Simple Probes for the Naked-Eye Detection of Cyanide Ion. Chemistry (Switzerland), 5(2), 978-986. https://doi.org/10.3390/chemistry5020066apa_pure
dc.identifier.issn2624-8549-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85163654667&doi=10.3390%2fchemistry5020066&partnerID=40&md5=e93e27911c608c3239be5f43bf57f2eb1
dc.identifier.otherhttps://www.mdpi.com/2624-8549/5/2/66/pdf?version=1682421956pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130588-
dc.description.abstractCyanide ions are known to be lethal for insects and mammals and harmful for the environment, and new methods for their selective detection are in high demand. Herein, the mechanosynthesis of simple Schiff’s bases-based probes S1–S3 for visual detection of CN− anion is reported. These probes were obtained by means of a reaction between isomeric 4,4-, 3,3- and 2,2-diaminobiphenyls and 4-nitrobenzaldehyde under ball milling conditions. The probes showed high selectivity and sensitivity toward CN− anion via a dramatic “yellow-to-dark purple” color change with a detection limit of 26 × 103, 8.7 × 103 and 14 × 103 ppm for S1–S3, respectively. The proposed mechanism of the detection suggests the deprotonation of a proton from an imine moiety, followed by the formation of charge transfer complexes (CTC). © 2023 by the authors.en
dc.description.sponsorshipMinistry of Education and Science of the Russian Federation, Minobrnauka: 075-15-2022-1118en
dc.description.sponsorshipThis research was funded by the Ministry of Science and Higher Education of the Russian Federation (Agreement # 075-15-2022-1118 accessed on 29 June 2022).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMDPIen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceChemistry2
dc.sourceChemistry (Switzerland)en
dc.subjectCOLOR CHANGEen
dc.subjectCYANIDE ION DETECTIONen
dc.subjectMECHANOSYNTHESISen
dc.subjectSCHIFF BASESen
dc.titleMechanosynthesis of Diaminobiphenyls-Based Schiff’s Bases as Simple Probes for the Naked-Eye Detection of Cyanide Ionen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/chemistry5020066-
dc.identifier.scopus85163654667-
local.contributor.employeeAl-Ithawi, W.K.A., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, Energy and Renewable Energies Technology Center, University of Technology-Iraq, Baghdad, 10066, Iraqen
local.contributor.employeeKhasanov, A.F., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeKovalev, I.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeNikonov, I.L., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeeKopchuk, D.S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeePlatonov, V.A., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeSantra, S., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeZyryanov, G.V., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeeRanu, B.C., Chemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federation, School of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, 700032, Indiaen
local.description.firstpage978-
local.description.lastpage986-
local.issue2-
local.volume5-
dc.identifier.wos001014173000001-
local.contributor.departmentChemical Engineering Institute, Ural Federal University, 19 Mira St, Yekaterinburg, 620002, Russian Federationen
local.contributor.departmentEnergy and Renewable Energies Technology Center, University of Technology-Iraq, Baghdad, 10066, Iraqen
local.contributor.departmentI. Ya. Postovsky Institute of Organic Synthesis of RAS (Ural Division), 22/20 S. Kovalevskoy/Akademicheskaya St, Yekaterinburg, 620219, Russian Federationen
local.contributor.departmentSchool of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, 700032, Indiaen
local.identifier.pure41541854-
local.identifier.eid2-s2.0-85163654667-
local.identifier.wosWOS:001014173000001-
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

Файлы этого ресурса:
Файл Описание РазмерФормат 
2-s2.0-85163654667.pdf1,32 MBAdobe PDFПросмотреть/Открыть


Лицензия на ресурс: Лицензия Creative Commons Creative Commons