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Synthesis of cobalt(III) complexes with novel open chain oxime ligands and metal-ligand coordination in aqueous solution
被引:10
|作者:
Kufelnicki, Aleksander
[1
]
Tomyn, Stefania V.
[2
]
Nedelkov, Ruslan V.
[2
]
Haukka, Matti
[3
]
Jaciubek-Rosinska, Jolanta
[1
]
Pajak, Marek
[1
]
Jaszczak, Jan
[1
]
Swiatek, Miroslawa
[1
]
Fritsky, Igor O.
[2
]
机构:
[1] Med Univ Lodz, Fac Pharm, Lab Phys & Biocoordinat Chem, PL-90151 Lodz, Poland
[2] Kiev Natl Taras Shevchenko Univ, Dept Chem, UA-01601 Kiev, Ukraine
[3] Univ Joensuu, Dept Chem, FI-80101 Joensuu, Finland
关键词:
Oxime ligands;
Cobalt(III) complexes;
Synthesis;
Cobalt(II);
Dioxygen;
Solution equilibria;
ALPHA-AMINO-ACIDS;
ARGINASE;
CAVITY;
D O I:
10.1016/j.ica.2010.04.002
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Cobalt(III) complexes with new open chain oxime ligands: N,N'-bis(2-hydroxyiminopropionyl)-1,2-aminoethane (H(2)pen) and N,N'-bis(2-hydroxyiminopropionyl)-1,3-diaminopropane (H(2)pap) have been investigated. Single crystals of Co(papH (1))(Im(2))center dot CH3OH (1) and Co(papH (1))(MEA)(2)center dot 1.5H(2)O (2) (where Im = imidazole, MEA = monoethanolamine) suitable for X-ray crystallography were grown by slow evaporation of methanol/water solutions at room temperature. The molecular structures have been determined using single-crystal X-ray diffraction methods. The potentiometric and spectrophotometric results in aqueous solution reveal that both of the open chain ligands show a very high efficacy in the coordination of Co(II) ions. As it has been indicated, differences between the two oxime ligands in complexing ability may be attributed to the longer -CH2-chain in H(2)pap and by that a better fit of the relatively large Co(II) ion to the accessible binding site. One of the complex species confirmed under inert atmosphere, namely of type Co(LH (1)) (where L = pap or pen), has been shown as the `` active" form, capable of dioxygen uptake followed by irreversible oxidation to Co(III). (C) 2010 Elsevier B. V. All rights reserved.
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页码:2996 / 3003
页数:8
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