Solid state tautomerism in 2-((phenylimino)methyl)naphthalene-1-ol
- Nedeltcheva, Daniela Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Sofia, Bulgaria
- Kamounah, Fadhil S. Department of Science, Systems and Models, Roskilde University, Denmark
- Mirolo, Laurent Department of Chemistry, University of Fribourg, Switzerland
- Fromm, Katharina M. Department of Chemistry, University of Fribourg, Switzerland
- Antonov, Liudmil Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Sofia, Bulgaria
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18.04.2009
Published in:
- Dyes and Pigments. - 2009, vol. 83, no. 1, p. 121-126
Tautomerism
Schiff bases
Intramolecular proton transfer
Crystallography
Spectroscopy
Photochromic dyes
English
The solid state tautomerism of 2-((phenylimino)methyl)naphthalene-1-ol was studied using X-ray measurements and absorption spectroscopy. In the solid state, the keto tautomer predominates. The observed shift in the equilibrium from the enol (dilute solution) to the keto (solid state) forms is explained by the formation of dye aggregates using ab initio quantum chemical calculations.
- Faculty
- Faculté des sciences et de médecine
- Department
- Département de Chimie
- Language
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- English
- Classification
- Chemistry
- License
- License undefined
- Identifiers
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- RERO DOC 13173
- DOI 10.1016/j.dyepig.2009.04.002
- Persistent URL
- https://folia.unifr.ch/unifr/documents/301262
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