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1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils
dc.creator | Jovanović, B.Z. | |
dc.creator | Tadić, Z.D. | |
dc.creator | Muškatirović, M.D. | |
dc.creator | Pešić, Mirjana | |
dc.creator | Bogdanović, S.I. | |
dc.date.accessioned | 2020-12-17T17:33:22Z | |
dc.date.available | 2020-12-17T17:33:22Z | |
dc.date.issued | 1988 | |
dc.identifier.issn | 0022-2860 | |
dc.identifier.uri | http://aspace.agrif.bg.ac.rs/handle/123456789/65 | |
dc.description.abstract | The 1H n.m.r. spectra of some 5-substituted-3-isopropyl-6-methyl uracils were determined in deuterated dimethyl sulfoxide (d6-DMSO). The substituents are: H, Cl, Br, I, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that relative chemical shift (Δδ) of N(1)-H proton of some of the examined compounds correlated linearly with Hammett σm constant for the substituents in position 5 of uracil ring. The correlation with the σm constant was interpreted as providing evidence that the inductive effect of the substituent on chemical shift is dominating one. | en |
dc.rights | restrictedAccess | |
dc.source | Journal of Molecular Structure | |
dc.title | 1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils | en |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.epage | 284 | |
dc.citation.issue | C | |
dc.citation.other | 174(C): 281-284 | |
dc.citation.rank | M23 | |
dc.citation.spage | 281 | |
dc.citation.volume | 174 | |
dc.identifier.doi | 10.1016/0022-2860(88)80171-6 | |
dc.identifier.scopus | 2-s2.0-45449122789 | |
dc.type.version | publishedVersion |