Tautomerism and Possible Polymorphism in Solid Hydroxypyridines and Pyridones Studied by 14N NQR
- Author
- SELIGER, Janez1 2 3 ; ZAGAR, Veselko1
[1] Jozef Stefan Institute, Jamova 39,, 1000 Ljubljana, Slovenia
[2] Faculty of Mathematics and Physics, University of Ljubljana, Jadranska 19, 1000 Ljubljana, Slovenia
[3] EN-FIST Centre of Excellence, Dunajska 156, 1000 Ljubljana, 1000 Ljubljana, Slovenia - Source
The journal of physical chemistry. A. 2013, Vol 117, Num 7, pp 1651-1658, 8 p ; ref : 67 ref
- ISSN
- 1089-5639
- Scientific domain
- General chemistry, physical chemistry; Materials; Atomic molecular physics
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Composé organique Constante couplage quadripolaire Dérivé de la pyridine Hétérocycle azote Liaison hydrogène Phase solide Spectre RQN Tautomérie cétoénolique Tautomérie imine énamine 3325 Pyridine(3-hydroxy)
- Keyword (en)
- Organic compounds Quadrupole coupling constant Pyridine derivatives Nitrogen heterocycle Hydrogen bonds Solid phase NQR spectrum Keto enol tautomerism Imine enamine tautomerism
- Keyword (es)
- Constante acoplamiento cuadripolar Piridina derivado Heterociclo nitrógeno Espectro RQN Tautomería ceto-enólica Tautomería imina enamina
- Classification
- Pascal
- 001 Exact sciences and technology / 001B Physics / 001B30 Atomic and molecular physics / 001B30C Molecular properties and interactions with photons / 001B30C25 Nuclear resonance and relaxation
- Discipline
- Atomic and molecular physics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 27130735
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jp3117038 
https://dx.doi.org/10.1021/jp3117038
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