Coordination Tendency of Some Biologically Important Zwitterionic Buffers toward Metal Ion Nucleotide Complexes at Different Temperatures

被引:11
|
作者
Azab, Hassan A. [1 ]
Anwar, Zeinab M. [1 ]
机构
[1] Suez Canal Univ, Fac Sci, Dept Chem, Ismailia, Egypt
来源
关键词
POLYBASIC OXYGEN ACIDS; TERNARY COMPLEXES; BINARY COMPLEXES; PRIMARY LIGANDS; NUCLEOBASES; STABILITY;
D O I
10.1021/je300830k
中图分类号
O414.1 [热力学];
学科分类号
摘要
The formation of binary and ternary complexes of Cu(II), Co(II), Mn(II), Zn(II), Ca(II), Mg(II), and Pd(II) with 4-morpholinoethane sulfonic acid (MES), 2-(cyclohexylamino)ethane sulfonic acid (CHES), and 3-[(N-tris)-(hydroxymethyl)methyl (amino)]-2-hydroxypropanesulfonic acid (TAPSO) as zwitterionic buffers and guanosine 5'-monophosphate (5'-GMP), inosine 5'-monophosphate (5'-IMP), and uridine 5'-mono-phosphate (5'-UMP) has been studied potentiometrically in the temperature range (288.15 to 318.15) K and at ionic strength I = 0.1 mol.dm(-3) (KNO3). Initial estimates of the formation constants of the resulting species and the dissociation constants of the studied ligands have been refined with the SUPERQUAD computer program. The experimental conditions were selected such that self-association of the nucleotides and their complexes was negligibly small; that is, the monomeric and protonated complexes were studied.
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页码:2890 / 2895
页数:6
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