Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/14975
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dc.rights.licenseBY-NC-ND-
dc.contributor.authorRadovanović M.-
dc.contributor.authorRistić, M-
dc.contributor.authorZlatar, Matija-
dc.contributor.authorHeinemann F.-
dc.contributor.authorMatović, Zoran-
dc.date.accessioned2022-09-13T11:39:56Z-
dc.date.available2022-09-13T11:39:56Z-
dc.date.issued2022-
dc.identifier.issn0352-5139-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/14975-
dc.description.abstractOnly one (trans(O5)-Na[Rh(ED3AP)]·3H2O) of possible two isomers was synthesized and characterized by single crystal X-ray analysis, IR and UV-Vis spectroscopy. Computational analysis of both isomers was performed with three levels of theory (B3LYP/TZV, BP86/TZV, OPBE/TZV), which gave consistent results. The more stable isomer by total energy and ligand field stabilization energy (LFSE) was trans(O5) which appeared in synthesis. The calculation of excited state energies complied with UV-Vis spectra, especially with OPBE functional. The results of excited state energy pointed out the differences among isomers in means of a splitting pattern of 1T2g excited state term. Both isomers have a strongly delocalized structure, according to the natural bonding orbital (NBO) analysis. NBO analysis shows that the trans(O5) isomer is more stable than trans(O5O6) for approx. 87 kJ/mol. Therefore, only the trans(O5) isomer is present in the reaction mixture.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceJournal of the Serbian Chemical Society-
dc.titleNew rhodium(III)-ED3AP complex: Crystal structure, characterization and computational chemistry-
dc.typearticle-
dc.identifier.doi10.2298/JSC211230003R-
dc.identifier.scopus2-s2.0-85133237581-
Appears in Collections:Faculty of Science, Kragujevac

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