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dc.creatorMiodragović Đenana U.
dc.creatorMilosavljević, Slobodan M.
dc.creatorMalinar, M.J.
dc.creatorCelap, MB
dc.creatorTodorović, Nevena M.
dc.creatorJuranić, N.
dc.date.accessioned2018-11-22T00:05:16Z
dc.date.available2018-11-22T00:05:16Z
dc.date.issued2002
dc.identifier.issn1024-2430
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/537
dc.description.abstractRotamer population of S-tyrosinato and S-phenylalaninato ligands side groups in diastereomers of (1,2-diaminoethane)bis(S-aminocarboxylato)cobalt(III) complexes is calculated by vicinal alpha and beta proton coupling constant analysis. The effect of noncovalent intra- and interligand interactions on the population of rotamers in D2O solution is discussed. It has been established that in all the complexes investigated the most abundant is rotamer t, in which aromatic voluminous moiety and carboxylic group are in an anti position. In almost all complexes the lowest content is of rotamer g, in which these two groups are in the nearest position. Relatively high population of rotamer b in complex 5 tyr, in spite of high steric hindrances, is due to intra- and interligand NH... pi interactions.en
dc.publisherTaylor & Francis Ltd, Abingdon
dc.rightsrestrictedAccess
dc.sourceEnantiomer
dc.subjectcobalt(III) complex diastereomersen
dc.subjectconformational analysisen
dc.subjectNMRen
dc.subjectNH ... pi interactionsen
dc.subjectS-phenylalanineen
dc.subjectS-tyrosineen
dc.titleMixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylatoen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЈураниц, Н; Малинар, МЈ; Милосављевиц, СМ; Целап, МБ; Тодоровиц, Н; Миодраговиц, ДУ;
dc.citation.volume7
dc.citation.issue6
dc.citation.spage375
dc.citation.epage382
dc.identifier.wos000180895200011
dc.identifier.doi10.1080/10242430215714
dc.citation.other7(6): 375-382
dc.citation.rankM22
dc.identifier.pmid12643314
dc.type.versionpublishedVersionen


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