Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7655
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dc.contributor.authorŞener, İzzet-
dc.contributor.authorAydin, G.-
dc.date.accessioned2019-08-16T12:31:08Z
dc.date.available2019-08-16T12:31:08Z
dc.date.issued2014-
dc.identifier.issn0975-1491-
dc.identifier.urihttps://hdl.handle.net/11499/7655-
dc.description.abstractObjective: The aim of the work was to designed and synthesized novel heterocyclic tetrakisazo dyes.en_US
dc.description.abstractMethods: 2,2'[(4,4'-dihydrazonebiphenyl)]-bis(3-iminobuthyronitrile) (1) were synthesized by diazotization of benzidine using hydrochloric acid in water. Compounds (1) reacted with hydrazine hydrate to afford the corresponding 4,4'-bis [3-methyl-5-amino-1-H-pyrazol-4-ylazo]biphenyl (2). Seven novel hetaryltetrakisazobenzidine Derivatives 3(a-g) were achieved by diazotization of 4,4'-bis [3-methyl-5-amino-1-H-pyrazol-4-ylazo]biphenyl and coupling with various coupling components.en_US
dc.description.abstractResults: The obtained hetaryltetrakisazo dyes 3(a-g) were characterized based on FT-IR, 1H-NMR, and mass spectroscopic techniques as well as elemental analysis. The solvatochromic behavior of these dyes in various solvents was examined. Acid-base effects on the visible absorption maxima of the dyes were also reported.en_US
dc.description.abstractConclusion: Synthesis and characterization of seven of these nine novel compounds synthesized, which are hetaryltetrakisazo dyes 3(a-g). © 2014,International Journal of Pharmacy and Pharmaceutical Sciences All Rights Reserved.en_US
dc.language.isoenen_US
dc.publisherInternational Journal of Pharmacy and Pharmaceutical Scienceen_US
dc.relation.ispartofInternational Journal of Pharmacy and Pharmaceutical Sciencesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiazo-coupling reactionen_US
dc.subjectDiazotizationen_US
dc.subjectPyrazoleen_US
dc.subjectSolvatochromismen_US
dc.subjectTetrakisazo dyesen_US
dc.subject4,4' bis [(2',4' dihyroxyquinoline 3') ylazo1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (2' hydroxynaphthaline 1' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (2' hydroxypyridine 3' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (3' methyl 5' hydroxy 1' h pyrazole 4' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (4' hydroxy 6' methyl 2' pyrone 3' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (4' hydroxycoumarine 3' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subject4,4' bis [3 methyl 5 (8' hydroxyquinoline 7' ylazo) 1 h pyrazole 4 ylazo] biphenylen_US
dc.subjectazo compounden_US
dc.subjecthetaryltetrakisazobenzidine derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectabsorptionen_US
dc.subjectArticleen_US
dc.subjectdiazotizationen_US
dc.subjectdrug synthesisen_US
dc.subjectinfrared spectroscopyen_US
dc.subjectmass spectrometryen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectsolvent effecten_US
dc.subjectthin layer chromatographyen_US
dc.subjectultraviolet spectrophotometryen_US
dc.titleSynthesis, Characterization and absorption properties of some novel heterocyclic tetrakisazo dyesen_US
dc.typeArticleen_US
dc.identifier.volume6en_US
dc.identifier.issue9en_US
dc.identifier.startpage540
dc.identifier.startpage540en_US
dc.identifier.endpage545en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-84907814918en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.dept17.01. Chemistry-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
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