Synthesis spectroscopic and molecular structure characterizations of some azo derivatives of 2 hydroxyacetophenone
Yazarlar (5)
Prof. Dr. Çiğdem ALBAYRAK KAŞTAŞ Sinop Üniversitesi, Türkiye
Ismail E. Gümrükçüoǧlu
Ondokuz Mayis Üniversitesi, Türkiye
Mustafa Odabaşoǧlu
Pamukkale Üniversitesi, Türkiye
Prof. Dr. Nazan Ocak Iskeleli Ondokuz Mayis Üniversitesi, Türkiye
Erbil Aǧar
Ondokuz Mayis Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Journal of Molecular Structure (Q3)
Dergi ISSN 0022-2860 Dergi Bilgileri (2009)
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 08-2009
Kabul Tarihi Yayınlanma Tarihi 01-08-2009
Cilt / Sayı / Sayfa 932 / 1 / 43–54 DOI 10.1016/j.molstruc.2009.05.043
Makale Linki http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=15&SID=N2PHr9GtJvTfxHUgNeq&page=2&doc=52&cacheurlFromRightClick=no
UAK Araştırma Alanları
Organik Kimya
Özet
Some novel azo compounds were prepared by the reaction of 2-hydroxyacetophenone with aniline and its substituted derivatives. The structures of synthesized azo compounds were determined by IR, UV–Vis, 1H NMR and 13C NMR spectroscopic techniques and the structures of some of these compounds were also determined by X-ray diffraction studies. Structural analysis using IR in solid state shows that the azo form is favoured in the azo compounds whereas UV–Vis analysis of the azo compounds in solution has shown that there is a azo and ionic form. The azo compounds in the basic solvents dimethylformamide (DMF) and dimethylsulfoxide (DMSO) are both azo and ionic form while these compounds in ethyl alcohol (EtOH) and chloroform (CHCl3) are only azo form.
Anahtar Kelimeler
2-Hydroxyacetophenone | Azo dyes | Azobenzene | Spectral characterization | X-ray analysis
Science Direct
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 25
Scopus 26
Google Scholar 29
Synthesis spectroscopic and molecular structure characterizations of some azo derivatives of 2 hydroxyacetophenone

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