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dc.contributor.advisorÜngören, Şevket Hakan
dc.contributor.authorDilekoğlu, Emine
dc.date.accessioned2021-05-07T08:25:05Z
dc.date.available2021-05-07T08:25:05Z
dc.date.submitted2011
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/596586
dc.description.abstractBu çalışmada potansiyel herbisit olarak yeni 1,2,4-triazin ve pirazin-2,3-dikarbonitril iskeletine sahip heterosiklik bileşikler sentezlenmiştir. Metot başlangıç maddesi olan bazı furan-2,3-dionların, S-metilizotiyosemikarbazit ve diaminomaleonitril ile yeniden halkalaşma reaksiyonuna dayanır. Buna ilave olarak sentezlenen pirazin-2,3-dikarbonitril bileşiklerinin hidrolizi edilerek bu bileşiklerin bazı türevleri elde edilmiştir.Sentezlenen yeni bileşikler moleküler spektroskopik metotlarla karakterize edilmiştir.
dc.description.abstractIn this study, novel 1,2,4-triazine and pyrazine-2,3-dicarbonitrile derivatives were synthesized as potential herbicides. The method was based on cyclocondensation of furan-2,3-diones with S-methylisothiosemicarbazide and diaminomaleonitrile. Moreover, the synthesized pyrazine-2,3-dicarbonitrile derivatives were transformed to its corresponding new derivatives by hydrolyze reactions.The synthesized new compounds were characterized with molecular spectroscopic methods.en_US
dc.languageTurkish
dc.language.isotr
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAttribution 4.0 United Statestr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectKimyatr_TR
dc.subjectChemistryen_US
dc.titlePotansiyel herbisit olarak yeni 1,2,4-triazin ve pirazin-2,3-dikarbonitril türevi heterohalkalı bileşiklerin sentezi
dc.title.alternativeSynthesise of 1,2,4-triazine and pyrazine-2,3-dicarbonitrile derivatives as potential herbicides
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentKimya Ana Bilim Dalı
dc.subject.ytmFuran-2,3-dione
dc.subject.ytm1,2,4-triazine
dc.identifier.yokid421628
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityBOZOK ÜNİVERSİTESİ
dc.identifier.thesisid300157
dc.description.pages80
dc.publisher.disciplineDiğer


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