Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/21192
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dc.contributor.authorFilipović, Ignjat-
dc.contributor.authorRadovanovic, Marko-
dc.contributor.authorDjukic, Maja-
dc.contributor.authorKlisurić, Olivera-
dc.contributor.authorStojković, Danijela-
dc.contributor.authorRistić, Marija-
dc.contributor.authorMatović, Zoran-
dc.contributor.editorČobeljić, Božidar-
dc.date.accessioned2024-10-11T08:34:54Z-
dc.date.available2024-10-11T08:34:54Z-
dc.date.issued2023-
dc.identifier.isbn978-86-912959-6-7en_US
dc.identifier.issn0354-5741en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/21192-
dc.description.abstractThis complex was synthesized following by the method described elsewhere [1]. To a solution of [Rh2(CH3COO)4(H2O)2] (0.0478 g, 0.10 mmol) in toluene (10 mL) the N-butylimidazole (0.0290 mL, 0.22 mmol) was added. The resulting mixture was stirred at room temperature for 1 hour until the reagents were completely dissolved. The solution was left at room temperature to evaporate slowly to a volume of ~ 5 mL and then stored overnight in the refrigerator. The precipitated purple crystals were filtered off under vacuum and washed with toluene and diethyl ether. The obtained crystals represent a complex of [Rh2(CH3COO)4(N-BuIm)]. Crystal data: monoclinic, space group P21/c, crystal size 0.25 × 0.27 × 0.40 mm3, a = 15.7537(6), b = 13.5490(5), c = 17.3153(7) Å, β = 110.366(5)°, V = 3464.9(3) Å3, Z = 4, ρ = 1.3234 g cm-3, μ = 0.992 mm-1, R = 0.0629, wR = 0.1645.en_US
dc.language.isoenen_US
dc.publisherSerbian Crystallographic Societyen_US
dc.titleSYNTHESIS AND CRYSTAL STRUCTURE OF [Rh2(CH3COO)4(N-BuIm)] COMPLEXen_US
dc.title.alternativeCИHTE3A И КРИСТАЛНА СТРУКТУРА [Rh2(CH3COO)4(N-BuIm)] КОМПЛЕКСАen_US
dc.typeconferenceObjecten_US
dc.description.versionPublisheden_US
dc.type.versionPublishedVersionen_US
Appears in Collections:Faculty of Science, Kragujevac

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