Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/13559
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dc.contributor.authorGobor, Ladislaven_US
dc.contributor.authorPetrović, Slobodanen_US
dc.contributor.authorNikolić, Aleksandaren_US
dc.contributor.authorAntonović, Dušanen_US
dc.contributor.authorMolnár-Gábor, Doraen_US
dc.date.accessioned2020-03-03T14:52:48Z-
dc.date.available2020-03-03T14:52:48Z-
dc.date.issued1999-05-25-
dc.identifier.issn00222860en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/13559-
dc.description.abstractThe article reports the results of a 1H NMR study of a series of recently synthesized N-alkyl pivaloylamides in carbon tetrachloride solution and in presence of O-electron donors (acetone and tetrahydrofuran). Chemical shifts for free NH and NH · · · O bonded protons were obtained. Equilibrium constants for 1 : 1 amide-acetone/tetrahydrofuran hydrogen bonded complexes, at 25°C were determined.en
dc.relation.ispartofJournal of Molecular Structureen
dc.title1H NMR study of N–H⋯O hydrogen bonding – N-alkyl pivaloylamide–ketone (ether) systemsen_US
dc.typeConference Paperen_US
dc.identifier.doi10.1016/S0022-2860(98)00944-2-
dc.identifier.scopus2-s2.0-0033603037-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0033603037-
dc.description.versionUnknownen_US
dc.relation.lastpage346en
dc.relation.firstpage343en
dc.relation.volume482-483en
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Collections:PMF Publikacije/Publications
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