Geometrical Structure Information Of 5-Phenyl-2-Pyridinamine Derivatives By Means Of FTIR.

T. Visser; J. F.C. Stavenuiter; G. Zomer

doi:10.1117/12.969396

1 December 1989 Geometrical Structure Information Of 5-Phenyl-2-Pyridinamine Derivatives By Means Of FTIR.

T. Visser, J. F.C. Stavenuiter, G. Zomer

Proceedings Volume 1145, 7th Intl Conf on Fourier Transform Spectroscopy; (1989) https://doi.org/10.1117/12.969396
Event: Seventh International Conference on Fourier and Computerized Infrared Spectroscopy, 1989, Fairfax, VA, United States

Abstract

Infrared N-H, O-H and C=0 absorption bands of N-substituted hydroxy-, acetyl- and acetoxy- pyridinamines and biphenyl amines have been studied. Band deconvolution has been applied to determine the presence of rotational isomers. Ortho methyl substitution and the position of the pyridine nitrogen atom are found to affect the orientation of the amino substituents.

Citation Download Citation

T. Visser, J. F.C. Stavenuiter, and G. Zomer "Geometrical Structure Information Of 5-Phenyl-2-Pyridinamine Derivatives By Means Of FTIR.", Proc. SPIE 1145, 7th Intl Conf on Fourier Transform Spectroscopy, (1 December 1989); https://doi.org/10.1117/12.969396

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