alexa Theoretical IR, UV, 1H And 13C-NMR Spectra Of Certain Schiff Bases Derived Substituted-2-aminophenol And Hydroxyl Benzaldehyde
ISSN: 2150-3494

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4th European Chemistry Congress
May 11-13, 2017 Barcelona, Spain

Dila Ercengiz, Halil Berber and Ulku Dilek Uysal
Anadolu University,Turkey
Posters & Accepted Abstracts: Chem Sci J
DOI: 10.4172/2150-3494-C1-009
Schiff bases are compounds formed by the condensation of an active carbonyl group with primary amine or N-substituted imine containing an imino group (R-C=N-). They have been used as ligands, liquid crystals, heterogeneous catalysts, high-performance organic light emitting diodes (OLED), and to design molecular ferromagnet, in catalysis and biological applications [1]. In this study, five Schiff bases (Figure 1) have been synthesized and characterized with 1H and 13C-NMR. These Schiff bases’ Gibbs Free Energies, Dipole moments, HOMO-LUMO values, theoretical IR, UV, 1H and 13C-NMR spectra have been researched by DFT method with Gaussian09 program (B3LYP/6-311++G(d,p)) [2] and compared than those with experimental values. Structure- reactivity relationship for these molecules was also searched.

Dila Ercengiz has completed her Bachelor’s degree in 2015 from Anadolu University. She is student of Anadolu University at Graduate School of Sciences.

Email: [email protected]

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