Publication:
Synthesis, Characterization, and Pharmacological Studies of Ferrocene-1H Hybrids

dc.authorscopusid55204383500
dc.authorscopusid7202490093
dc.authorscopusid7201618346
dc.authorscopusid37101705000
dc.authorscopusid57194548522
dc.authorscopusid57201620841
dc.authorscopusid36197168600
dc.contributor.authorHaque, A.
dc.contributor.authorHsieh, M.-F.
dc.contributor.authorHassan, S.I.
dc.contributor.authorHaque Faizi, M.S.
dc.contributor.authorSaha, A.
dc.contributor.authorDege, N.
dc.contributor.authorAhmad Rather, J.A.
dc.date.accessioned2020-06-21T13:17:59Z
dc.date.available2020-06-21T13:17:59Z
dc.date.issued2017
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Haque] Ashanul, Department of Chemistry, Sultan Qaboos University, Muscat, Oman; [Hsieh] Mingfa, Department of Biomedical Engineering, Chung Yuan Christian University, Taoyuan, Taiwan; [Hassan] Syed Imran, Department of Chemistry, Sultan Qaboos University, Muscat, Oman; [Haque Faizi] Md Serajul, Department of Chemistry, Sultan Qaboos University, Muscat, Oman; [Saha] Anannya, Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, WB, India; [Dege] Necmi, Department of Physics, Ondokuz Mayis University Faculty of Science and Arts, Samsun, Turkey; [Ahmad Rather] Jahangir Ahmad, Department of Chemistry, Sultan Qaboos University, Muscat, Oman; [Khan] Muhammad S., Department of Chemistry, Sultan Qaboos University, Muscat, Omanen_US
dc.description.abstractA series of ferrocene-1H-1,2,3-triazole hybrids namely 1-(4-nitrophenyl)-4-ferrocenyl-1H-1,2,3-triazole (1), 1-(4,4′-dinitro-2-biphenyl)-4-ferrocenyl-1H-1,2,3-triazole (2), 1-(3-chloro-4-fluorophenyl)-4-ferrocenyl-1H-1,2,3-triazole (3), 1-(4-bromophenyl)-4-ferrocenyl-1H-1,2,3-triazole (4) and 1-(2-nitrophenyl)-4-ferrocenyl-1H-1,2,3-triazole (5) were designed and synthesized by copper-catalyzed azide alkyne cycloaddition (CuAAC) reaction. All the new hybrids were characterized by microanalyses, NMR (1H and 13C), UV–vis, IR, ESI-MS and electrochemical techniques. Crystal structure of the compound (3) was solved by single crystal X-ray diffraction method. The structural (single crystal) and spectroscopic (UV–Vis. and IR) properties of the compound 3 have been analyzed and compared by complementary quantum modeling. Hybrids 1–5 exhibited low toxicity and demonstrated neuroprotective effect. © 2017 Elsevier B.V.en_US
dc.identifier.doi10.1016/j.molstruc.2017.06.027
dc.identifier.endpage545en_US
dc.identifier.issn0022-2860
dc.identifier.scopus2-s2.0-85020741173
dc.identifier.scopusqualityQ1
dc.identifier.startpage536en_US
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2017.06.027
dc.identifier.volume1146en_US
dc.identifier.wosWOS:000406985800064
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofJournal of Molecular Structureen_US
dc.relation.journalJournal of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnti-Inflammatoryen_US
dc.subjectClick-Chemistryen_US
dc.subjectCopper-Catalyzed Azide-Alkyne Cycloaddition Reactionen_US
dc.subjectFerroceneen_US
dc.subjectToxicityen_US
dc.subjectViabilityen_US
dc.titleSynthesis, Characterization, and Pharmacological Studies of Ferrocene-1H Hybridsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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