2,2’-[Tiyobis P-Fenilennitrilometilidin ]Bis 4-Kloro/ Bromo/Metil/Nitro/Metoksi Fenol'ün Spektroskopik Özellikleri

4’-diaminodifenil sülfit ile 2-hidroksi-5-sübstitüebenzaldehit ve 2-hidroksinaftaldehitin tepkimesi ile yeni Schiff bazları sentezlendi. Bileşiklerin yapıları elementel analiz, FT-IR, 1H NMR, 13C NMR ile aydınlatıldı. Bileşiklerin polar ve apolar çözücülerdeki asidik ve bazik ortamlardaki UV-vis. spektrumları incelendi. UV-vis. sonuçlarına göre çözücü ortamında enol-imin tautomerinin daha baskın olduğu görüldü

Anahtar Kelimeler:

Schiff bazı, Daimin bileşikleri, Benzaldehit, Keto-enol tautomer

Spectroscopic Properties of 2,2’-[Thiobis P- Phenylenenitrilomethylidyne ]Bis 4-Chloro/ Bromo/Methyl/Nitro/Methoxy Phenol

Novel Schiff base has been synthesized from the reaction of 4,4’-diaminodiphenyl sulfide with 2-hydroxy- 5-substituebenzaldehyde and 2-hydroxynaphtaldehyde. The compounds were characterized by elemental analysis, FT-IR, 1H NMR,13C NMR. The UV-visible spectra of the compounds were studied in polar and nonpolar solvents in acidic and basic media. İt is point out that the enol-imine tautomer is dominant only in the solution form the compound 1a-e.

Keywords:

Schiff base, Diamine compounds, Benzaldehyde, Keto-enol tautomer,

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