Publication: 2-Hidroksi-5-Metilbenzaldehit İçeren Bazı Yeni Schiff Bazlarının Sentezi ve Spektroskopik Özelliklerinin İncelenmesi
Abstract
Bu çalışmada, 2-hidroksi-5-metilbenzaldehit; 2-amino-5-metilfenol, 2-amino-4-nitrofenol, 5-amino-2-metilfenol, 3,4-dimetoksibenzilamin, 3-klor-4-metilanilin, 2-aminobenzonitril, 2-metil-3-nitroanilin, 4-metilanilin, 4-(triflormetil)anilin ve 3,5-difloranilin ile reaksiyona sokularak karşılık gelen azometin bileşikleri elde edildi. Sentezlenen bileşikler, (Z)-6-(((2-hidroksi-4-metilfenil)amino)metilen)-4-metilsiklohekza-2,4-dien-1-on, (Z)-6-(((2-hidroksi-5-nitrofenil)amino)metilen)-4-metilsiklohekza-2,4-dien-1-on, (Z)-2-(((3-hidroksi-4-metilfenil)imino)metil)-4-metilfenol, (E)-2-(((3,4-dimetoksibenzil)imino)metil)-4-metilfenol, (E)-2-(((3-klor-4-metilfenil)imino)metil)-4-metilfenol, (E)-2-((2-hidroksi-5-metilbenziliden)amino) benzonitril, (E)-4-metil-2-(((2-metil-3-nitrofenil)imino)metil)fenol, (E)-4-metil-2-(((4-metilfenil)imino)metil)fenol, (E)-4-metil-2-(((4-(triflormetil)fenil)imino) metil)fenol ve (E)-2-(((3,5-diflorfenil)imino)metil)-4-metilfenol'dur. Sentezlenen bu azometin bileşiklerinin yapıları IR, 1H-NMR, 13C-NMR ve UV-Vis spektroskopik teknikleri kullanılarak aydınlatıldı. Uygun çözücülerde tek kristalleri hazırlanan bileşiklerin kristalografik ve moleküler yapıları X-Işınları difraksiyon yöntemiyle de belirlendi.
In this study, 2-hydroxy-5-methylbenzaldehyde was reacted with 2-amino-5-methylphenol, 2-amino-4-nitrophenol, 5-amino-2-methylphenol, 3,4-dimethoxybenzylamine, 3-chloro-4-methylaniline, 2-aminobenzonitrile, 2-methyl-3-nitroaniline, 4-methylaniline, 4-(trifluoromethyl)aniline and 3,5-difluoroaniline to give the corresponding azomethine compounds. The synthesized compounds are (Z)-6-(((2-hydroxy-4-methylphenyl)amino)methylene)-4-methylcyclohexa-2,4-dien-1-one, (Z)-6-(((2-hydroxy-5-nitrophenyl)amino)methylene)-4-methylcyclohexa-2,4-dien-1-one, (Z)-2-(((3-hydroxy-4-methylphenyl)imino)methyl)-4-methylphenol, (E)-2-(((3,4-dimethoxybenzyl)imino)methyl)-4-methylphenol, (E)-2-(((3-chloro-4-methylphenyl)imino)methyl)-4-methylphenol, (E)-2-((2-hydroxy-5-methylbenzylidene)amino)benzonitrile, (E)-4-methyl-2-(((2-methyl-3-nitrophenyl) imino)methyl)phenol, (E)-4-methyl-2-((((2-methyl-3-nitrophenyl)imino)methyl) phenol, (E)-4-methyl-2-(((4-methylphenyl)imino)methyl)phenol, (E)-4-methyl-2-((((4-(trifluoromethyl) phenyl)imino)methyl)phenol and (E)-2-(((3,5-difluorophenyl) imino)methyl)-4-methylphenol. The structures of these synthesized azomethine compounds were determined by IR, 1H-NMR, 13C-NMR and UV-Vis spectroscopic techniques.The crystallographic and molecular structures of the azomethine compounds,which single crystalls had been prepared in suitable solvents, were also determined by X-Ray diffraction method.
In this study, 2-hydroxy-5-methylbenzaldehyde was reacted with 2-amino-5-methylphenol, 2-amino-4-nitrophenol, 5-amino-2-methylphenol, 3,4-dimethoxybenzylamine, 3-chloro-4-methylaniline, 2-aminobenzonitrile, 2-methyl-3-nitroaniline, 4-methylaniline, 4-(trifluoromethyl)aniline and 3,5-difluoroaniline to give the corresponding azomethine compounds. The synthesized compounds are (Z)-6-(((2-hydroxy-4-methylphenyl)amino)methylene)-4-methylcyclohexa-2,4-dien-1-one, (Z)-6-(((2-hydroxy-5-nitrophenyl)amino)methylene)-4-methylcyclohexa-2,4-dien-1-one, (Z)-2-(((3-hydroxy-4-methylphenyl)imino)methyl)-4-methylphenol, (E)-2-(((3,4-dimethoxybenzyl)imino)methyl)-4-methylphenol, (E)-2-(((3-chloro-4-methylphenyl)imino)methyl)-4-methylphenol, (E)-2-((2-hydroxy-5-methylbenzylidene)amino)benzonitrile, (E)-4-methyl-2-(((2-methyl-3-nitrophenyl) imino)methyl)phenol, (E)-4-methyl-2-((((2-methyl-3-nitrophenyl)imino)methyl) phenol, (E)-4-methyl-2-(((4-methylphenyl)imino)methyl)phenol, (E)-4-methyl-2-((((4-(trifluoromethyl) phenyl)imino)methyl)phenol and (E)-2-(((3,5-difluorophenyl) imino)methyl)-4-methylphenol. The structures of these synthesized azomethine compounds were determined by IR, 1H-NMR, 13C-NMR and UV-Vis spectroscopic techniques.The crystallographic and molecular structures of the azomethine compounds,which single crystalls had been prepared in suitable solvents, were also determined by X-Ray diffraction method.
Description
Citation
WoS Q
Scopus Q
Source
Volume
Issue
Start Page
End Page
138
