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dc.contributor.authorPavelek, Lubomír
dc.contributor.authorLadányi, Vít
dc.contributor.authorNečas, Marek
dc.contributor.authorVallová, Silvie
dc.contributor.authorWichterle, Kamil
dc.date.accessioned2016-06-13T10:03:27Z
dc.date.available2016-06-13T10:03:27Z
dc.date.issued2016
dc.identifier.citationPolyhedron. 2016, vol. 107, p. 89-96.cs
dc.identifier.issn0277-5387
dc.identifier.urihttp://hdl.handle.net/10084/111639
dc.description.abstractUsing the reactions of 2,4-dihydrazino-(R)-s-triazine (R – methoxy (DHMT)) with salicylaldehyde and o-vanillin ligands 2,4-Bis(2-hydroxybenzylidenehydrazino)-6-methoxy-s-triazin (L1) and 2,4-Bis(2-hydroxy-3-methoxybenzylidenehydrazino)-6-methoxy-s-triazin (L2) were obtained. Using the reaction of 2,4-dihydrazino-(R)-s-triazine (R – amino (DHAT)) with o-vanillin ligand 2,4-Bis(2-hydroxy-3-methoxybenzylidenehydrazino)-6-amino-s-triazine (L3) was obtained. By the reactions of the prepared ligands, derivatives of hydrazo-s -triazine, with uranyl acetate or nitrate, three new complexes were prepared. X-ray diffraction shows that the View the MathML sourceUO22+ ion is in a pentagonal bipyramidal coordination environment. Two oxygen atoms of the View the MathML sourceUO22+ ion occupy the axial positions and three atoms of nitrogen and two atoms of oxygen construct the equatorial plane. The uranyl(VI) complexes were characterized by single-crystal X-ray diffraction, UV–vis, fluorescence and IR spectroscopy. Thermal stabilities of the complexes were investigated using thermogravimetric analysis.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesPolyhedroncs
dc.relation.urihttp://dx.doi.org/10.1016/j.poly.2016.01.014cs
dc.rightsCopyright © 2016 Elsevier Ltd. All rights reserved.cs
dc.subjectUranyl(VI)cs
dc.subjectComplexescs
dc.subjectTriazine ligandscs
dc.subjectX-ray structurecs
dc.subjectOptical propertiescs
dc.titleDioxouranium complexes with pentadentate s-triazine Schiff base ligands: Synthesis, crystal structure and optical propertiescs
dc.typearticlecs
dc.identifier.doi10.1016/j.poly.2016.01.014
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume107cs
dc.description.lastpage96cs
dc.description.firstpage89cs
dc.identifier.wos000374613700011


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