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Pregled bibliografske jedinice broj: 379588

Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods


Novak, Predrag; Pičuljan, Katarina; Hrenar, Tomica; Smrečki, Vilko
Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods // Croatica chemica acta, 82 (2009), 2; 477-483 (međunarodna recenzija, članak, znanstveni)


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Naslov
Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods

Autori
Novak, Predrag ; Pičuljan, Katarina ; Hrenar, Tomica ; Smrečki, Vilko

Izvornik
Croatica chemica acta (0011-1643) 82 (2009), 2; 477-483

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
salicylaldehyde 4-phenylthiosemicarbazones ; NMR ; DFT ; hydrogen bonds

Sažetak
Solution state structure and hydrogen-bonding in 4- and 5-methoxysalicylaldehyde 4- phenylthiosemicarbazones, 1 and 2, have been studied by a combined use of NMR spectroscopy and DFT calculations. It has been shown that both compounds existed in hydroxy-thione tautomeric form in solution as previously found in solid state. Two kinds of hydrogen bonds were found to exist in solution, i. e. intra- and inter- molecular. The DFT calculations and chemical shift values support the conclusion that three center hydrogen bonds were formed between the studied compounds and the solvent used, involving OH and NH groups. The solution state structures of 1 and 2 were found to differ slightly from those observed in the solid state which was attributed to a low barrier of rotation around the N– N bond.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
MZOS-098-0982929-2917 - Spektroskopija NMR i modeliranje bioaktivnih molekula (Plavšić, Dejan, MZOS ) ( CroRIS)
MZOS-119-1191342-1083 - Interakcije i dizajn bioaktivnih molekula (Novak, Predrag, MZOS ) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Profili:

Avatar Url Katarina Pičuljan (autor)

Avatar Url Vilko Smrečki (autor)

Avatar Url Tomica Hrenar (autor)

Avatar Url Predrag Novak (autor)

Poveznice na cjeloviti tekst rada:

Hrčak

Citiraj ovu publikaciju:

Novak, Predrag; Pičuljan, Katarina; Hrenar, Tomica; Smrečki, Vilko
Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods // Croatica chemica acta, 82 (2009), 2; 477-483 (međunarodna recenzija, članak, znanstveni)
Novak, P., Pičuljan, K., Hrenar, T. & Smrečki, V. (2009) Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods. Croatica chemica acta, 82 (2), 477-483.
@article{article, author = {Novak, Predrag and Pi\v{c}uljan, Katarina and Hrenar, Tomica and Smre\v{c}ki, Vilko}, year = {2009}, pages = {477-483}, keywords = {salicylaldehyde 4-phenylthiosemicarbazones, NMR, DFT, hydrogen bonds}, journal = {Croatica chemica acta}, volume = {82}, number = {2}, issn = {0011-1643}, title = {Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods}, keyword = {salicylaldehyde 4-phenylthiosemicarbazones, NMR, DFT, hydrogen bonds} }
@article{article, author = {Novak, Predrag and Pi\v{c}uljan, Katarina and Hrenar, Tomica and Smre\v{c}ki, Vilko}, year = {2009}, pages = {477-483}, keywords = {salicylaldehyde 4-phenylthiosemicarbazones, NMR, DFT, hydrogen bonds}, journal = {Croatica chemica acta}, volume = {82}, number = {2}, issn = {0011-1643}, title = {Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods}, keyword = {salicylaldehyde 4-phenylthiosemicarbazones, NMR, DFT, hydrogen bonds} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus





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