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dc.contributor.advisorBektaş, Hakan
dc.contributor.authorKurt, Zafer
dc.date.accessioned2020-12-04T13:45:50Z
dc.date.available2020-12-04T13:45:50Z
dc.date.submitted2019
dc.date.issued2019-11-08
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/87888
dc.description.abstractBu tez 5,6-dikloro-2- (4-florobenzil) -lH-benzimidazol'den başlayarak, asetat (1), hidrazid (2,3), 1,3,4-oksadiazol (4, 5), tiyosemikarbazit (6a-c), 1,2,4-triazol (7a-c) ve 1,3,4-tiadiazol (8a-c) sentezlenmiştir. Sentezlenen bu hidrazit bileşiğinin değişik aldehitlerle reaksiyonlarından schiff bazlari sentezlendi. Ayrıca yine hidrazit bileşiği değişik izotiyosyanatlarla reaksiyonu ve ardından halka kapamaları ile değişik heterosiklik bileşikler sentezlendi.Yapılan çalışmalar spektroskopik ( IR,UV,NMR..) yöntemler yardımıyla aydınlatımış olup çalışmalarımız başarılı şekilde yapılımıştır
dc.description.abstractIn this study, benzimidazole compounds were obtained from the reaction between 4,5-dichloro-o-phenylenediamine and ethylcyclopropylethaneimidiate hydrochloride by the help of the N-H proton. After that, these benzimidazole compounds were fistly converted to ester functionality and then hydrazide functionality. The reaction between obtained hydrazide derivatives and different aldehydes resulted in the formation of Schiff bases. In addition to these reactions, different heterocyclic compounds were synthesized with the reaction between hydrazides and isothiocyanates..Studies spectroscopic (IR, UV, ...) are methods that help illuminate ...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.titleYeni benzimidazol türevlerinin sentezi
dc.title.alternativeSynthesis of novel benzi̇mi̇dazole derivatives
dc.typemasterThesis
dc.date.updated2019-11-08
dc.contributor.departmentKimya Anabilim Dalı
dc.identifier.yokid10267499
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityGİRESUN ÜNİVERSİTESİ
dc.identifier.thesisid575859
dc.description.pages67
dc.publisher.disciplineDiğer


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