1960 年 80 巻 9 号 p. 1275-1278
Of the three absorption bands, ν1, ν2 and ν3, present in the region of 1600-1500cm-1 in α, β-unsaturated β-amino-ketones formed by substitution of enolic hydroxyl in 1, 3-cyclohexanediones with anilino, benzylamino, and phenethylamino group, ν3 corresponds to the amide-II band in the secondary amide, and ν1, and ν2 were considered to be explanable in a same manner as the coupling vibration of C=O and C=C described in Part I of this series. The intensity of this in-phase vibration was found to be proportional to the aromaticity of the substituted amines.