Yayın:
Synthesis, structural analysis, and absorption properties of disperse benzothiazol-derivative mono-azo dyes

Basit Görünüm
dc.contributor.authorŞener, İzzet
dc.contributor.authorŞener, Nesrin
dc.contributor.authorGür, Mahmut
dc.date.accessioned2026-01-04T12:27:47Z
dc.date.issued2018-12-01
dc.description.abstractAbstract A series of carbocyclic amines was reacted with 3-aminocrotonitrile to give the 2-arylhydrazone-3-ketiminobutyronitriles 1(a–m). Separately, 2-aminobenzothiazole was treated with hydrazine monohydrate to afford 2-hydrazinobenzothiazole. Then, compounds 1(a–m) were reacted with 2-hydrazinobenzimidazole under reflux in ethanol to give the 1-(1,3-benzothiazol-2-yl)-3-methyl-4-arylazo-5-aminopyrazole compounds 2(a–m). The structures of the synthesized compounds were investigated using FT-IR and 1H NMR spectroscopic methods and elemental analysis. Furthermore, the absorption profiles of the dyes in different solvents and in acidic and basic media were investigated.
dc.description.urihttps://doi.org/10.1016/j.molstruc.2018.04.052
dc.description.urihttps://dx.doi.org/10.1016/j.molstruc.2018.04.052
dc.identifier.doi10.1016/j.molstruc.2018.04.052
dc.identifier.endpage17
dc.identifier.issn0022-2860
dc.identifier.openairedoi_dedup___::073f5fef2f9d37233e13fbb6e2cbd414
dc.identifier.orcid0000-0003-0540-7523
dc.identifier.orcid0000-0001-9942-6324
dc.identifier.scopus2-s2.0-85054573372
dc.identifier.startpage12
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37062
dc.identifier.volume1174
dc.identifier.wos000449132500004
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofJournal of Molecular Structure
dc.rightsCLOSED
dc.subject.sdg3. Good health
dc.titleSynthesis, structural analysis, and absorption properties of disperse benzothiazol-derivative mono-azo dyes
dc.typeArticle
dspace.entity.typePublication
local.api.response{"authors":[{"fullName":"İzzet Şener","name":"İzzet","surname":"Şener","rank":1,"pid":{"id":{"scheme":"orcid","value":"0000-0003-0540-7523"},"provenance":null}},{"fullName":"Nesrin Şener","name":"Nesrin","surname":"Şener","rank":2,"pid":null},{"fullName":"Mahmut Gür","name":"Mahmut","surname":"Gür","rank":3,"pid":{"id":{"scheme":"orcid","value":"0000-0001-9942-6324"},"provenance":null}}],"openAccessColor":null,"publiclyFunded":false,"type":"publication","language":{"code":"eng","label":"English"},"countries":null,"subjects":[{"subject":{"scheme":"FOS","value":"01 natural sciences"},"provenance":null},{"subject":{"scheme":"FOS","value":"0104 chemical sciences"},"provenance":null},{"subject":{"scheme":"SDG","value":"3. Good health"},"provenance":null}],"mainTitle":"Synthesis, structural analysis, and absorption properties of disperse benzothiazol-derivative mono-azo dyes","subTitle":null,"descriptions":["Abstract A series of carbocyclic amines was reacted with 3-aminocrotonitrile to give the 2-arylhydrazone-3-ketiminobutyronitriles 1(a–m). Separately, 2-aminobenzothiazole was treated with hydrazine monohydrate to afford 2-hydrazinobenzothiazole. Then, compounds 1(a–m) were reacted with 2-hydrazinobenzimidazole under reflux in ethanol to give the 1-(1,3-benzothiazol-2-yl)-3-methyl-4-arylazo-5-aminopyrazole compounds 2(a–m). The structures of the synthesized compounds were investigated using FT-IR and 1H NMR spectroscopic methods and elemental analysis. Furthermore, the absorption profiles of the dyes in different solvents and in acidic and basic media were investigated."],"publicationDate":"2018-12-01","publisher":"Elsevier BV","embargoEndDate":null,"sources":["Crossref"],"formats":null,"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_14cb","label":"CLOSED","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":{"name":"Journal of Molecular Structure","issnPrinted":"0022-2860","issnOnline":null,"issnLinking":null,"ep":"17","iss":null,"sp":"12","vol":"1174","edition":null,"conferencePlace":null,"conferenceDate":null},"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"doi_dedup___::073f5fef2f9d37233e13fbb6e2cbd414","originalIds":["S0022286018304940","10.1016/j.molstruc.2018.04.052","50|doiboost____|073f5fef2f9d37233e13fbb6e2cbd414","2796732154"],"pids":[{"scheme":"doi","value":"10.1016/j.molstruc.2018.04.052"}],"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":18,"influence":3.4707979e-9,"popularity":1.15024426e-8,"impulse":10,"citationClass":"C4","influenceClass":"C4","impulseClass":"C4","popularityClass":"C4"}},"instances":[{"pids":[{"scheme":"doi","value":"10.1016/j.molstruc.2018.04.052"}],"license":"Elsevier TDM","type":"Article","urls":["https://doi.org/10.1016/j.molstruc.2018.04.052"],"publicationDate":"2018-12-01","refereed":"peerReviewed"},{"alternateIdentifiers":[{"scheme":"mag_id","value":"2796732154"},{"scheme":"doi","value":"10.1016/j.molstruc.2018.04.052"}],"type":"Article","urls":["https://dx.doi.org/10.1016/j.molstruc.2018.04.052"],"refereed":"nonPeerReviewed"}],"isGreen":false,"isInDiamondJournal":false}
local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus

Dosyalar

Koleksiyonlar

Publications