1959
DOI: 10.1039/jr9590001275
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250. The frequencies and intensities of the N–H stretching vibrations in primary amines. Part II. Polycyclic aromatic amines

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Cited by 20 publications
(5 citation statements)
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“…That there is in all these cases some sp2 character to the N-H bonds in aromatic amines is shown by the higher values of in them as compared to that in cyclohexylamine. The variations noticed in antisymmetric N-H stretching vibrations and intensities are also attributed to steric effects (185) in peri amines. The exceptional behavior of 3-aminopyrene noticed here has been also pointed out in another investigation (199).…”
Section: XXXVII Xxxviiimentioning
confidence: 83%
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“…That there is in all these cases some sp2 character to the N-H bonds in aromatic amines is shown by the higher values of in them as compared to that in cyclohexylamine. The variations noticed in antisymmetric N-H stretching vibrations and intensities are also attributed to steric effects (185) in peri amines. The exceptional behavior of 3-aminopyrene noticed here has been also pointed out in another investigation (199).…”
Section: XXXVII Xxxviiimentioning
confidence: 83%
“…Elliott and Mason (185) and Krueger (356) have studied the N-H stretching frequencies and intensities of hindered and unhindered polycyclic aromatic amines.…”
Section: XXXVII Xxxviiimentioning
confidence: 99%
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“…The spectroscopic features in the wavenumber region around 3000 cm -1 most prominently reflect the difference of terminal groups (amine or amine hydrochloride). It is well-established that amino compounds exhibit two NH-associated modes: antisymmetric ν as (NH) and symmetric ν s (NH). , The ratio of ν s to ν as has been reduced theoretically to ν s /ν as = 0.98 for various amino compounds . The corresponding ratio for the doublet peaks occurring at 3328 and 3276 cm -1 in 1a is ν s /ν as = 3276/3328 = 0.984.…”
Section: Resultsmentioning
confidence: 98%
“…It is well-established that amino compounds exhibit two NH-associated modes: antisymmetric ν as (NH) and symmetric ν s (NH). 25,26 The ratio of ν s to ν as has been reduced theoretically to ν s /ν as ) 0.98 for various amino compounds. 27 The corresponding ratio for the doublet peaks occurring at 3328 and 3276 cm -1 in 1a is ν s /ν as ) 3276/3328 ) 0.984.…”
Section: Resultsmentioning
confidence: 99%