1961
DOI: 10.1016/0371-1951(61)80120-3
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The infrared spectra of some chlorinated derivatives of s-triazine

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Cited by 26 publications
(7 citation statements)
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“…1(A)] shows two characteristic peaks at 3334 and 3205 cm −1 , respectively. The former can be attributed to the NH stretching of the free amino group, and the latter can be assigned to the NH stretching of the hydrogen‐bonded amino group; this is in good agreement with the literature data 30, 31. In ACHT [Fig.…”
Section: Resultssupporting
confidence: 90%
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“…1(A)] shows two characteristic peaks at 3334 and 3205 cm −1 , respectively. The former can be attributed to the NH stretching of the free amino group, and the latter can be assigned to the NH stretching of the hydrogen‐bonded amino group; this is in good agreement with the literature data 30, 31. In ACHT [Fig.…”
Section: Resultssupporting
confidence: 90%
“…Similar results were obtained in the infrared study of other chlorinated s ‐triazine derivatives, and Heckle et al31 believed that the behavior of this ring band resulted from a mass effect associated with the relatively heavy chlorine atoms corresponding to differing degrees of chlorination, which agreed well with this finding. Another band worth mentioning in ADCT is the 850‐cm −1 peak, which is a characteristic band of triazine derivatives containing two or three chlorine atoms bonded directly to ring carbon atoms 31. As expected, in ACHT, because of the presence of only one chlorine atom in the structure, the 850‐cm −1 band disappears.…”
Section: Resultssupporting
confidence: 85%
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“…Even with these problems in mind, the resulting spectrum strongly suggests the presence of etheral, hydroxy-, and chlorotriazine derivatives. It has been reported that 2,4,6-substituted triazines exhibit bands in the 800-cm"1 region due to an out-of-plane ring vibration (21, 23). The absolute frequency of the vibration is strongly dependent upon the types of substituents present on the triazine ring.…”
Section: Ch Rljhí íN/mentioning
confidence: 99%