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EN
The UV-photoinduced prototropic isomerization of 1,3-diphenyl pyrazol-5-one (DPhP) embedded in polyvinyl chloride (PVC) film is studied by means of difference in IR spectral analysis. The initially existing CH-form in non-irradiated compound is transformed to NH-form, and a hydrochloride salt is stabilized because of the photodegradation of the PVC. An additional comparative IR spectral study of DPhP in different solutions as well as of its hydrochloride salts in solid state is also carried out.
EN
4-Acetaminopyridine dihydrate and its protonated form, stabilized as the hydrochloride salt have been synthesized and spectroscopic elucidated in solution and in the solid-state by means of the inear-polarized solid state IR-spectroscopy (IR-LD), UV-spectroscopy, TGA, DSC, and the positive and negative ESI MS. Quantum chemical calculations were used to obtain the electronic structure, vibrational data and the electronic spectra. The spectroscopic and theoretical data are compared with the structure of the first compound obtained by single crystal X-ray diffraction. The effect of Npy protonation on the optical and magnetic properties of a 4-acetaminopyridine is discussed.
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