Synthesis, Characterization, and Spectroscopic Investigation of New Iron(III) and Copper(II) Complexes of a Carboxylate Rich Ligand and Their Interaction with Carbohydrates in Aqueous Solution

被引:21
|
作者
Stewart, Christopher D. [1 ]
Arman, Hadi [1 ]
Bawazir, Huda [1 ]
Musie, Ghezai T. [1 ]
机构
[1] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
关键词
METAL-SACCHARIDE CHEMISTRY; D-XYLOSE ISOMERASE; DINUCLEAR COPPER(II); CRYSTAL-STRUCTURES; MAGNETIC-PROPERTIES; ZINC(II) COMPLEXES; IRON; COORDINATION; BIOLOGY; MODEL;
D O I
10.1021/ic501351a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New tetra-iron(III) (K-4[1]center dot 25H(2)O center dot(CH3)(2)CO and K-3[2]center dot 3H(2)O center dot(OH)) and di-copper(II) (Na-3[3]center dot 5H(2)O) complexes as carbohydrate binding models have been synthesized and fully characterized used several techniques including single crystal X-ray crystallography. Whereas K-4[1]center dot 25H(2)O center dot(CH3)(2)CO and Na-3[3]center dot 5H(2)O are completely water-soluble, K-3[2]center dot 3H(2)O center dot(OH) is less soluble in all common solvents including water. The binding of substrates, such as D-mannose, D-glucose, D-xylose, and xylitol with the water-soluble complexes in different reaction conditions were investigated. In aqueous alkaline media, complexes K-4[1]center dot 25H(2)O center dot(CH3)(2)CO and Na-3[3]center dot 5H(2)O showed coordination ability toward the applied substrates. Even in the presence of stoichiometric excess of the substrates, the complexes form only 1:1 (complex/substrate) molar ratio species in solution. Apparent binding constants, pK(app), values between the complexes and the substrates were determined and specific mode of substrate binding is proposed. The pK(app) values showed that D-mannose coordinates strongest to K-4[1]center dot 25H(2)O center dot(CH3)(2)CO and Na-3[3]center dot 5H(2)O. Syntheses, characterizations and detailed substrate binding study using spectroscopic techniques and single crystal X-ray diffraction are reported.
引用
收藏
页码:10974 / 10988
页数:15
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