Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12190
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dc.contributor.authorBugarčić Z.-
dc.contributor.authorDivac, Vera-
dc.contributor.authorKostic, Marina-
dc.contributor.authorJanković, Nenad-
dc.contributor.authorHeinemann F.-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorStojanović-Radić, Zorica-
dc.date.accessioned2021-04-20T20:13:55Z-
dc.date.available2021-04-20T20:13:55Z-
dc.date.issued2015-01-01-
dc.identifier.issn01620134-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12190-
dc.description.abstract© 2014 Elsevier Inc. Two novel Pd(II) complexes with 2-(phenylselanylmethyl)oxolane and 2-(phenylselanylmethyl)oxane as ligands were synthesized. The crystal and molecular structure of the complexes has been determined by single crystal X-ray diffraction. It turned out for both complexes that the two ligands are coordinated to Pd via Se atoms in a trans-fashion and the other two trans-positions are occupied by Cl ions. Detailed 1D- and 2D-NMR analyses revealed the existence of equilibrating trans-diastereomeric species differing in the configuration at four chiral centers (selenium and carbon) in the solution of the complexes. A computational study was also undertaken to assess the relative stabilities of the mentioned stereoisomeric species. The antimicrobial properties of the complexes were investigated against a series of human pathogenic bacterial and fungal strains. The complexes were shown to possess promising broad spectrum moderate antimicrobial activity that is more pronounced against fungal organisms. The noted activity could be completely attributed to the Pd(II) center, whereas the ligands probably mediate the transportation of a Pd(II) species across cell membranes.-
dc.relation.ispartofJournal of Inorganic Biochemistry-
dc.rightsrestrictedAccess-
dc.titleSynthesis, crystal and solution structures and antimicrobial screening of palladium(II) complexes with 2-(phenylselanylmethyl)oxolane and 2-(phenylselanylmethyl)oxane as ligands-
dc.typearticle-
dc.identifier.doi10.1016/j.jinorgbio.2014.11.002-
dc.identifier.scopus84914141815-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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