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Synthesis and characterization of some novel cadmium(II) complexes with 3-hydroxypicolinic acid (3-OHpicH). Crystal and molecular structures of [CdI(3-OHpic)(3-OHpicH)(H2O)]2, [Cd(3-OHpic)2(H2O)2] and [Cd(3-OHpic)2]n (CROSBI ID 135577)

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Kukovec, Boris-Marko ; Popović, Zora ; Pavlović, Gordana ; Vinković, Marijana ; Vikić-Topić, Dražen Synthesis and characterization of some novel cadmium(II) complexes with 3-hydroxypicolinic acid (3-OHpicH). Crystal and molecular structures of [CdI(3-OHpic)(3-OHpicH)(H2O)]2, [Cd(3-OHpic)2(H2O)2] and [Cd(3-OHpic)2]n // Polyhedron, 27 (2008), 5; 1479-1488. doi: 10.1016/j.poly.2008.01.021

Podaci o odgovornosti

Kukovec, Boris-Marko ; Popović, Zora ; Pavlović, Gordana ; Vinković, Marijana ; Vikić-Topić, Dražen

engleski

Synthesis and characterization of some novel cadmium(II) complexes with 3-hydroxypicolinic acid (3-OHpicH). Crystal and molecular structures of [CdI(3-OHpic)(3-OHpicH)(H2O)]2, [Cd(3-OHpic)2(H2O)2] and [Cd(3-OHpic)2]n

Cadmium(II) complexes of 3-hydroxypicolinic acid, namely [CdI(3-OHpic)(3-OHpicH)(H2O)]2 (1), [Cd(3-OHpic)2(H2O)2] (2) and [Cd(3-OHpic)2]n (3) were prepared and characterized by spectroscopic methods (IR, NMR) and their molecular and crystal structures were determined by X-ray crystal structure analysis. Complexes 1 and 2 were prepared in similar reaction conditions using different cadmium(II) salts: cadmium(II) iodide and cadmium(II) acetate dihydrate, respectively, while 3 was prepared by recrystallization of 2 from N, N-dimethylformamide solution. Various coordination modes of 3-OHpicH in 1–3 were established in the solid state: bidentate N, O-chelated mode in 1 and 2, monodentate mode through the carboxylate O atom from zwitterionic ligand in 1 and bidentate N, O-chelated and bridging mode in 3. In the DMF solution of all prepared complexes, only monodentate mode of 3-OHpicH binding to cadmium(II) through the carboxylate O atom was established by 1H, 13C, 15N and 113Cd NMR spectroscopy.

cadmium(II) complexes ; 3-hydroxypicolinic acid ; IR spectroscopy ; 1H ; 13C ; 15N ; 113Cd NMR spectroscopy ; crystal structures

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Podaci o izdanju

27 (5)

2008.

1479-1488

objavljeno

0277-5387

10.1016/j.poly.2008.01.021

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