Nitroaniline derivatives of 2-oxo-1-naphthaldimines - molecular self-assembling via C-H...O intermolecular hydrogen bonds and stabilization of O-H...N and N-H...O tautomers in solution and solid state (CROSBI ID 101820)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Popović, Zora ; Pavlović, Gordana ; Roje, Vibor ; Došlić, Nađa ; Matković-Čalogović, Dubravka ; Leban, Ivan
engleski
Nitroaniline derivatives of 2-oxo-1-naphthaldimines - molecular self-assembling via C-H...O intermolecular hydrogen bonds and stabilization of O-H...N and N-H...O tautomers in solution and solid state
Three Schiff-bases of the Ar-CH=N-Ar type were synthesized from 2-hydroxy-1-naphthaldehyde and o- m- and p-nitroaniline in order to investigate the changes in the keto-amine/enol-imine tautomeric equilibrium caused by the introduction of the electron-withdrawal nitro group.
Schiff-bases ; 2-hydroxy-1-naphthaldehyde ; X-ray crystallography ; IR ; UV/VIS ; NMR-spectroscopy ; DFT calculations
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