Title of article :
A thermodynamic and crystallographic study of complexes of the highly preorganized ligand 8-hydroxyquinoline-2-carboxylic acid
Author/Authors :
McDonald، نويسنده , , F. Crisp and Applefield، نويسنده , , Rachel C. and Halkides، نويسنده , , Christopher J. and Reibenspies، نويسنده , , Joseph H. and Hancock، نويسنده , , Robert D.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
The metal ion complexing properties of the ligand HQC (8-hydroxyquinoline-2-carboxylic acid) are reported. The structures of [Zn(HQCH)2] · 3H2O (1) and [Cd(HQCH)2] · 3H2O (2) were determined (HQCH = HQC with phenol protonated). Both 1 and 2 are triclinic, space group P 1 ¯ , with Z = 2. For 1 a = 7.152(3), b = 9.227(4), c = 15.629(7) Å, α = 103.978(7)°, β = 94.896(7)°, γ = 108.033(8)°, R = 0.0499. For 2 a = 7.0897(5), b = 9.1674(7), c = 16.0672(11) Å, α = 105.0240(10)°, β = 93.9910(10)°, γ = 107.1270(10)°, R = 0.0330. In 1 the Zn has a distorted octahedral coordination geometry, with Zn–N of 2.00 and 2.15 Å, and Zn–O to the protonated phenolic oxygens of 2.431 and 2.220 Å. The structure of 2 is similar, with Cd–N bonds of 2.220 and 2.228 Å, with Cd–O bonds to the protonated phenolate oxygens of 2.334 and 2.463 Å. The structures of 1 and 2, and isomorphous Ni(II) and Co(II) HQC complexes reported in the literature, show very interesting short (<2.5 Å) O–O distances in H-bonds involving the protons on the coordinated phenolates and lattice water molecules. These are discussed in relation to the possible role of short low-energy H-bonds in alcohol dehydrogenase in mediating the transfer of the hydroxyl proton of the alcohol to an adjacent serine oxygen.
rmation constants for HQC are determined by UV–Visible spectroscopy at 25 °C in 0.1 M NaClO4 with Mg(II), Ca(II), Sr(II), Ba(II), La(III), Gd(III), Zn(II), Cd(II), Ni(II), Cu(II), and Pb(II). These show greatest stabilization with metal ions with an ionic radius above 1.0 Å. This is as would be expected from the fact that HQC forms two five-membered chelate rings on complex-formation, which favors larger metal ions. The ligand design concept of using rigid aromatic backbones in ligands to achieve high levels of preorganization, and hence the high log K values (for a tridentate ligand) and strong metal ion selectivities observed for HQC, is discussed.
Keywords :
nickel , 8-hydroxyquinoline , Gadolinium , 8-Hydroxyquinoline-2-carboxylic acid , Zinc , Ligand design , strontium , Calcium , barium , Magnesium , Lead , Copper , lanthanum , X-ray crystal structure , Ligand preorganization , formation constants , Metal ion recognition , Cadmium
Journal title :
INORGANICA CHIMICA ACTA
Journal title :
INORGANICA CHIMICA ACTA