Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10811
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dc.contributor.authorŞener, N.-
dc.contributor.authorErişkin, Selinay-
dc.contributor.authorGür, M.-
dc.contributor.authorŞener, İ.-
dc.date.accessioned2019-08-16T13:33:04Z
dc.date.available2019-08-16T13:33:04Z
dc.date.issued2018-
dc.identifier.issn0022-152X-
dc.identifier.urihttps://hdl.handle.net/11499/10811-
dc.identifier.urihttps://doi.org/10.1002/jhet.3129-
dc.description.abstract5,11,17,23-Tetra-tert-butyl-25,26,27,28-tetrahydroxycalix[4]arene and 25,26,27,28-tetrahydroxycalix[4]arene were synthesized based on previous literature. Firstly, several azo dyes were synthesized, and then, these dyestuffs were chlorinated through reaction with thionyl chloride. Secondly, the azo compounds bonded with methylene chloride and reacted with 25,26,27,28-tetrahydroxycalix[4]arene, and then, six novel disazocalix[4]arene derivatives 4(a–f) were achieved. Their structures were characterized as Fourier transform infrared, 1H-NMR, and elemental analysis. In this study, we investigated the solvatochromic properties of the compounds and the acid–base effect on their ultraviolet–visible absorption by using six solvents. © 2018 Wiley Periodicals, Inc.en_US
dc.language.isoenen_US
dc.publisherHeteroCorporationen_US
dc.relation.ispartofJournal of Heterocyclic Chemistryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectacetic aciden_US
dc.subjectacetonitrileen_US
dc.subjectazo dyeen_US
dc.subjectcalixareneen_US
dc.subjectchloroformen_US
dc.subjectchromogenic substrateen_US
dc.subjectdichloromethaneen_US
dc.subjectdimethyl sulfoxideen_US
dc.subjectdisazocalix[4]arene derivativeen_US
dc.subjectheterocyclic amineen_US
dc.subjectmethanolen_US
dc.subjectn,n dimethylformamideen_US
dc.subjectunclassified drugen_US
dc.subjectArticleen_US
dc.subjectchemical bonden_US
dc.subjectchemical structureen_US
dc.subjectchlorinationen_US
dc.subjectelemental analysisen_US
dc.subjectinfrared spectroscopyen_US
dc.subjectpHen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectsynthesisen_US
dc.subjecttautomeren_US
dc.subjectultraviolet spectrophotometryen_US
dc.titleNovel disubstituted calix[4]arenes containing chromogenic groups on the lower rim: Synthesis, structural identification, and absorption propertiesen_US
dc.typeArticleen_US
dc.identifier.volume55en_US
dc.identifier.issue4en_US
dc.identifier.startpage988
dc.identifier.startpage988en_US
dc.identifier.endpage994en_US
dc.identifier.doi10.1002/jhet.3129-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85041852227en_US
dc.identifier.wosWOS:000430179800027en_US
dc.identifier.scopusqualityQ4-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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