Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8268
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dc.contributor.authorŞener, İzzet-
dc.contributor.authorŞener, Nesrin-
dc.contributor.authorErişkin, Selinay-
dc.date.accessioned2019-08-16T12:37:52Z
dc.date.available2019-08-16T12:37:52Z
dc.date.issued2013-
dc.identifier.issn0143-7208-
dc.identifier.urihttps://hdl.handle.net/11499/8268-
dc.identifier.urihttps://doi.org/10.1016/j.dyepig.2012.08.015-
dc.description.abstractIn this study, a convenient method for the synthesis of thirteen novel tetrakisazo dyes containing 25,27-bis-(4-nitrobenzyloxy)-26,28-dihydroxycalix[4] arene have been described. 5,11,17,23-Tetra-tert-butyl-25,26,27,28- tetrahydroxycalix[4]arene, 25,26,27,28-tetrahydroxycalix[4]arene and 25,27-bis-(4-nitrobenzyloxy)-26,28-dihydroxycalix[4]arene were synthesized. 2-arylhydrazone-3-ketiminobutyronitriles 1(a-m) were synthesized and reacted with hydrazine hydrate to afford the corresponding 5-amino-4-arylazo-3-methyl-1- H-pyrazoles 2(a-m). Thirteen novel hetaryltetrakisazocalix[4]arene derivatives 6(a-m) were achieved by diazotisation of 5-amino-4-arylazo-3-methyl-1-H- pyrazoles using nitrosylsulphuric acid, coupling with 25,27-bis-(4- nitrobenzyloxy)-26,28-dihydroxycalix[4]arene. The obtained hetaryltetrakisazocalix[4]arene dyes 6(a-m) were characterized based on FT-IR, 1H NMR and Mass spectroscopic techniques as well as Elemental Analysis. The solvatochromic behaviour of these dyes in various solvents was examined. Acid-base effect on the visible absorption maxima of the dyes were also reported. © 2012 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofDyes and Pigmentsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAzocalix[4]arenesen_US
dc.subjectDiazo-coupling reactionen_US
dc.subjectDiazotizationen_US
dc.subjectDisazo dyesen_US
dc.subjectPyrazoleen_US
dc.subjectSolvaatochromismen_US
dc.subjectPyrazolesen_US
dc.subjectHydratesen_US
dc.subjectAzo dyesen_US
dc.titleSynthesis and absorption spectra of some novel hetaryltetrakisazocalix[4] arene derivativesen_US
dc.typeArticleen_US
dc.identifier.volume96en_US
dc.identifier.issue1en_US
dc.identifier.startpage256
dc.identifier.startpage256en_US
dc.identifier.endpage263en_US
dc.authorid0000-0003-0540-7523-
dc.authorid0000-0001-5370-6048-
dc.identifier.doi10.1016/j.dyepig.2012.08.015-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-84866000365en_US
dc.identifier.wosWOS:000310409100035en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept17.01. Chemistry-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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