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NMR and quantum chemical studies of hydrogen bonding in acetylacetone and benzoylacetone derived enaminones (CROSBI ID 615641)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa

Jednačak, Tomislav ; Lazić, Vedrana ; Jurković, Mihaela ; Hrenar, Tomica ; Parlov Vuković, Jelena ; Novak, Predrag NMR and quantum chemical studies of hydrogen bonding in acetylacetone and benzoylacetone derived enaminones // Program and book of abstracts / Smrečki, Vilko ; Vikić-Topić, Dražen (ur.). Zagreb: Institut Ruđer Bošković, 2014. str. 16-16

Podaci o odgovornosti

Jednačak, Tomislav ; Lazić, Vedrana ; Jurković, Mihaela ; Hrenar, Tomica ; Parlov Vuković, Jelena ; Novak, Predrag

engleski

NMR and quantum chemical studies of hydrogen bonding in acetylacetone and benzoylacetone derived enaminones

Enaminones represent an important class of organic molecules with interesting biological properties, such as anticonvulsant, antimicrobial, antioxidant, antitumor and cytogenetic activity. They might exist in two tautomeric forms: keto-amine and enol- imine. The structure and hydrogen bonding of acetylacetone and benzoylacetone derived enaminones in DMSO and CDCl3 solutions have been studied by a combination of NMR spectroscopy and quantum chemical (PM6 and DFT) methods. It has been demonstrated that the investigated compounds mainly existed in the localised keto-amine tautomeric form. Down-field chemical shifts of NH and OH protons and significant line-broadening have clearly indicated that both groups formed hydrogen bonds, which has further been supported by quantum chemical calculations. Concentration and temperature dependent NMR measurements have shown that amine protons are involved in strong intramolecular hydrogen bonding of the NH•••O=C type in both solvents. On the other hand, hydroxyl protons are engaged in weaker intermolecular hydrogen bonds with solvent molecules in DMSO, while in chloroform intermolecular interactions between two molecules are dominant. The presented results can further be used for better understanding and exploiting properties these compounds possess, especially their bioactivity.

enaminones; hydrogen bonding; NMR spectroscopy; quantum chemical studies

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Podaci o prilogu

16-16.

2014.

objavljeno

Podaci o matičnoj publikaciji

Program and book of abstracts

Smrečki, Vilko ; Vikić-Topić, Dražen

Zagreb: Institut Ruđer Bošković

978-953-7941-03-01

Podaci o skupu

16th Central European NMR Symposium and 16th Central European Bruker NMR Users Meeting

poster

16.10.2014-17.10.2014

Hrvatska

Povezanost rada

Kemija