Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorPütün, Ayşe Eren
dc.contributor.authorBereket, Gözen
dc.contributor.authorÖzbay, Nurgül
dc.date.accessioned2019-10-20T14:27:56Z
dc.date.available2019-10-20T14:27:56Z
dc.date.issued1996
dc.identifier.issn1303-6017
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TXpZMk1EZzQ=
dc.identifier.urihttps://hdl.handle.net/11421/17930
dc.description.abstractThe acidity constants of 4,5-diphenyl imidazole, 2,4,5-triphenyl imidazole, and 2,4,5-triphenyl imidazole derivatives in nitrobenzene, acetonitrile and glacial acetic acid were determined. Perchloric acid, prepared in 1,4-dioxane, was used as the titrant for the measurement which were done in acetonitrile; perchloric acid, prepared in nitrobenzene, was used as the titrant for the measurements that were done in nitrobenzene and perchloric acid, prepared in glacial acetic acid, was used as the titrant for the measurements which were done in glacial acetic acid. The pKa values were obtained from the half neutralization potentials which were obtained from an analysis of the potentiometric titrations. The ranging of the increasing acidic strengths were determined by considering whether the compounds had a substituent on 4, 5 position or not.en_US
dc.description.abstractThe acidity constants of 4,5-diphenyl imidazole, 2,4,5-triphenyl imidazole, and 2,4,5-triphenyl imidazole derivatives in nitrobenzene, acetonitrile and glacial acetic acid were determined. Perchloric acid, prepared in 1,4-dioxane, was used as the titrant for the measurement which were done in acetonitrile; perchloric acid, prepared in nitrobenzene, was used as the titrant for the measurements that were done in nitrobenzene and perchloric acid, prepared in glacial acetic acid, was used as the titrant for the measurements which were done in glacial acetic acid. The pKa values were obtained from the half neutralization potentials which were obtained from an analysis of the potentiometric titrations. The ranging of the increasing acidic strengths were determined by considering whether the compounds had a substituent on 4, 5 position or not.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMühendisliken_US
dc.subjectKimyaen_US
dc.titlePotentiometric titration of some imidazole derivatives in nonaqueous solventen_US
dc.typearticleen_US
dc.relation.journalCommunications Series:B Chemistry and Chemical Engineeringen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Kimya Bölümüen_US
dc.identifier.volume42en_US
dc.identifier.issue1-2en_US
dc.identifier.startpage1en_US
dc.identifier.endpage7en_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US]


Bu öğenin dosyaları:

Thumbnail

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster