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

Novak, Predrag; Pičuljan, Katarina; Hrenar, Tomica; Smrečki, Vilko (2009) Structure and Hydrogen Bonding Interactions in Methoxysalicylaldehyde Thiosemicarbazone Derivatives in Solution by NMR and DFT Methods. Croatica Chemica Acta, 82 (2). p. 477. ISSN 0011-1643

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Abstract

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. 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.

Item Type: Article
Uncontrolled Keywords: salicylaldehyde 4-phenylthiosemicarbazones; NMR; DFT; hydrogen bonds; nuclear-magnetic-resonance; chemical-shifts; ionic-solutions; complexes; solvent; salicylaldehyde-4-phenylthiosemicarbazone; salicylaldehyde; continuum; bases; state
Subjects: NATURAL SCIENCES > Chemistry
Divisions: NMR Center
Projects:
Project titleProject leaderProject codeProject type
Spektroskopija NMR i modeliranje bioaktivnih molekula[76010] Dejan Plavšić098-0982929-2917MZOS
Interakcije i dizajn bioaktivnih molekula[176404] Predrag Novak119-1191342-1083MZOS
Depositing User: Vilko Smrečki
Date Deposited: 18 Oct 2013 11:48
Last Modified: 12 Feb 2014 11:28
URI: http://fulir.irb.hr/id/eprint/815

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