2018
DOI: 10.5937/zasmat1801119v
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Solvatochromism of 5-(4-substituted arylazo)-4-phenyl-6-methyl-3-cyano-2-pyridones

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“…The 1 H NMR spectrum of the ligand showed clear signals involved singlet at δ (2.5) ppm belong to the proton of solvent (DMSO) and multiples signals at δ (7.3-7.9) ppm which were assigned to aromatic protons of phenyl rings.The proton of amine group (N-H) for the imidazole ring appeared in the chemical displacement(13.3 ppm) [21;22]. while the protons of the two methoxy group appeared at the chemical displacement(3.75 ppm) [23] as shown in Figure .( 2).…”
Section: H-nmr Spectrum Of Ligandmentioning
confidence: 99%
“…The 1 H NMR spectrum of the ligand showed clear signals involved singlet at δ (2.5) ppm belong to the proton of solvent (DMSO) and multiples signals at δ (7.3-7.9) ppm which were assigned to aromatic protons of phenyl rings.The proton of amine group (N-H) for the imidazole ring appeared in the chemical displacement(13.3 ppm) [21;22]. while the protons of the two methoxy group appeared at the chemical displacement(3.75 ppm) [23] as shown in Figure .( 2).…”
Section: H-nmr Spectrum Of Ligandmentioning
confidence: 99%