1967
DOI: 10.1016/0584-8539(67)80370-2
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Contribution à l'etude des spectres de vibration du thiazole

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Cited by 28 publications
(14 citation statements)
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“…tableaux 3 et 4). Soulignons, en faveur de I'attribution de la frtquence 1236 cm-' une vibration de dtformation 6(CH), dans le spectre de l'isothiazole, que l'oscillation 6(CH) la plus tlevte de nombreux dtrivts heterocycliques pentagonaux, est observte vers 1250 f 20 cm-' (19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31). Par analogie, nous relions aussi un mouvement 6(CH), la suite vers 1200 cm-', composte de bandes i.r.…”
Section: Dknombrement Des Vibrationsunclassified
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“…tableaux 3 et 4). Soulignons, en faveur de I'attribution de la frtquence 1236 cm-' une vibration de dtformation 6(CH), dans le spectre de l'isothiazole, que l'oscillation 6(CH) la plus tlevte de nombreux dtrivts heterocycliques pentagonaux, est observte vers 1250 f 20 cm-' (19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31). Par analogie, nous relions aussi un mouvement 6(CH), la suite vers 1200 cm-', composte de bandes i.r.…”
Section: Dknombrement Des Vibrationsunclassified
“…1) et devient fine, symCtrique et beaucoup plus intense, dans celui du dideutkrio-4,5 isothiazole a 1'Ctat dissous dans un solvant neutre. C'est ce comportement, analogue a celui de certaines absorptions y(CH) dans les hCtCrocycles thiazoliques (19)(20), qui nous a incitCs a choisir, pour la vibration y(CD), cette frCquence plut6t que celle, plus basse, a 541 cm-', qui a Ct C rattachke a l'oscillation de noyau I ? , .…”
Section: Vibrations De Symktrie A"unclassified
“…In this case, the Raman spectra were obtained using less Since the isotropic to nematic phase transformation occurs near 5% concentration, the spectral changes cannot be associated with the change in the intermolecular interaction, but rather with the structure of the polymer. On the basis of the vibrational spectra obtained for biphenyl and heterocyclic model compounds [26][27][28][29][30], the Raman bands observed were assignable to the stretching vibrations of the heterocyclic group, the phenyl ring and the C-C bond linking them [12].…”
Section: Protonation Effectmentioning
confidence: 99%
“…The angle predicted from conformational energy calculations is 600 [20], larger than actually measured. It appears that intermolecular interactions tend to keep the angle low in the solid state [28,29]. When the material is stressed, or in material lacking orientational order, it is reasonable to assign the changing polarization to a disruption of the intermolecular forces or to a direct weakening of the bond connecting two rings, thus affecting the coplanarity of the two rings.…”
Section: Stress Induced Structural Changesmentioning
confidence: 99%
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