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Proceedings Paper

Geometrical Structure Information Of 5-Phenyl-2-Pyridinamine Derivatives By Means Of FTIR.
Author(s): T. Visser; J. F.C. Stavenuiter; G. Zomer
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Paper 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.

Paper Details

Date Published: 1 December 1989
PDF: 2 pages
Proc. SPIE 1145, 7th Intl Conf on Fourier Transform Spectroscopy, (1 December 1989); doi: 10.1117/12.969396
Show Author Affiliations
T. Visser, National Institute for Public Health and Environmental Protection (The Netherlands)
J. F.C. Stavenuiter, National Institute for Public Health and Environmental Protection (The Netherlands)
G. Zomer, National Institute for Public Health and Environmental Protection (The Netherlands)


Published in SPIE Proceedings Vol. 1145:
7th Intl Conf on Fourier Transform Spectroscopy

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