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dc.contributor.authorIbis, Cemil
dc.contributor.authorAyla, Sibel Sahinler
dc.date.accessioned2021-03-05T16:20:06Z
dc.date.available2021-03-05T16:20:06Z
dc.date.issued2011
dc.identifier.citationIbis C., Ayla S. S. , "The Synthesis of New Thiosubstituted Compounds with Butadienyl and Butenynyl Groups", PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, cilt.186, ss.58-66, 2011
dc.identifier.issn1042-6507
dc.identifier.otherav_c01f178b-5199-485d-869a-d4a8bb049f44
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/127526
dc.identifier.urihttps://doi.org/10.1080/10426501003781624
dc.description.abstractMono(thio)substituted butadiene 3a, tetrakis(thio)substituted butadiene 4b, and bis(thio)substituted butadiene 10j were synthesized from 1,1,3,3,4,4-hexachloro butene and aromatic thiols in dimethylformamide at room temperature in the presence of triethylamine. Thiosubstituted butenyne compounds 5c, 6a, 7a,h, and 11i and butadiene compounds 3f,g, 4d, 8g, 9d, and 10i were synthesized from 1,1,3,3,4,4-hexachloro butene and different thiols in EtOH with NaOH solution. The thiosubstituted butadienes 13e and 14f were obtained from the reactions of 2H-1,1,3,4,-tetrachloro-4-bromo-butadiene and thiols in EtOH/H2O solution of NaOH. The structures of the new compounds were determined by microanalysis, FT-IR, UV/Vis, 1H NMR, 13C NMR, 19F NMR, MS, and fluorescence spectrophotometry. GRAPHICAL ABSTRACT[image omitted].
dc.language.isoeng
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.subjectBiyoinorganik Kimya
dc.subjectİnorganik Kimya
dc.subjectKİMYA, ORGANİK
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, İNORGANİK VE NÜKLEER
dc.titleThe Synthesis of New Thiosubstituted Compounds with Butadienyl and Butenynyl Groups
dc.typeMakale
dc.relation.journalPHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume186
dc.identifier.issue1
dc.identifier.startpage58
dc.identifier.endpage66
dc.contributor.firstauthorID198697


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