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Complexation studies of 3-substitutedβ-diketones with selected d- and f-metal ions

✍ Scribed by Grzegorz Pawlicki; Bartosz Staniszewski; Katarzyna Witt; Włodzimierz Urbaniak; Stefan Lis


Book ID
111491436
Publisher
Versita
Year
2011
Tongue
English
Weight
277 KB
Volume
65
Category
Article
ISSN
0366-6352

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✦ Synopsis


Abstract

Results of spectroscopic investigations related to complex compositions of 3-substituted derivatives of pentane-2,4-dione (β-diketonate) complexes with chosen d- and f-metal ions are presented. Ligands 3-allylacetylacetone (3all-acac) and 3-benzylacetylacetone (3ben-acac) were prepared and used for the complexation study with Cu(II), Co(II), Nd(III), and Ho(III) metal ions. Based on the absorption spectra of lanthanide ions in their hypersensitive transitions, with the use of computer assisted target factor analysis (CAT) and absorption spectra of the ligands with Cu(II) and Co(II), the verification of complex compositions and the determination of their stability constants were achieved. In case of Nd(III) and Ho(III) complexes with β-diketone ligands, absorption of their maxima were studied in the range of hypersensitive transitions 4 I 9/2 → 4 F 7/2 + 4 S 3/2 (λ max ∼ 734 nm and 748 nm) for Nd(III) and in the range of 435–465 nm, corresponding to the hypersensitive transition 5 G 6 → 5 I 8 (λ max ∼ 450 nm), for Ho(III).


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## Abstract Metal complexes of some divalent metal ions (Co, Ni, Cu, Zn, Hg, and Pd) with isatin-β-thiosemicarbazone (ITS) as the Schiff base have been investigated potentiometrically and spectrophotometrically. The dissociation constants of the ligand and formation constants of the metal complexes