Ternary complexes in solution. VIII. Complex formation between the copper(II)-2,2'-bipyridyl 1:1 complex and ligands containing oxygen and/or nitrogen donor atoms

1970 ◽  
Vol 9 (5) ◽  
pp. 1238-1243 ◽  
Author(s):  
Rolf Griesser ◽  
Helmut Sigel

1981 ◽  
Vol 46 (5) ◽  
pp. 1107-1115 ◽  
Author(s):  
Rolf Karlíček ◽  
Miroslav Polášek ◽  
Vladimír Jokl

The formation of N-carboxymethylaminoacetohydroxamic acid complexes in solutions with excess copper(II) or iron(III) ions or both of them was studied. In the presence of Cu(II), the binuclear complex Cu2H-1L+ was identified; in the ternary system, the complex CuFeH-1L+ was found. This complex formation is necessarily associated with the ligand structure >N-CH2.CO-NHOH and with a new property of hydroxamic acids of this type - detachment of two hydrogen ions from one carbohydroxamic functional group.



2018 ◽  
Vol 34 (6) ◽  
pp. 2782-2788
Author(s):  
Sapna Tomar ◽  
Padma Sikarwar

Potentiometeric investigation on the complex formation equilibria involving Co(II), Ni(II), Cu(II) & Zn(II) with ethylenediaamine-N,N,N1,N1-tetraacetic acid and melonic acid have been made in solution at three different temps viz. (150, 350, 450C). Important thermodynamic parameters namely, change in Gibb’s free energy (DG0), change in enthalpy (DH0) and change in entropy (DS0) and stability constant have been determined potentiometrically at ionic strength of 0.1 M (KNO3).



2000 ◽  
Vol 165 (2) ◽  
pp. 253-260 ◽  
Author(s):  
JJ Bond ◽  
S Meka ◽  
RC Baxter

Many tumours secrete IGF-II in incompletely processed precursor forms. The ability of these pro-IGF-II forms to complex with the six IGF binding proteins (IGFBPs) is poorly understood. In this study, pro-IGF-II has been extracted from the serum and tumour tissue of two patients with non-islet cell tumour hypoglycaemia. These samples were used to study binary complex formation with IGFBPs-1 to -6 using competitive IGF-II binding assays and ternary complex formation with IGFBP-3 and IGFBP-5. In each case, IGFBPs-1 to -6 showed little difference in their ability to form binary complexes with recombinant IGF-II or tumour-derived pro-IGF-II forms, when the preparations were standardised according to IGF-II immunoreactivity. As previously described, ternary complex formation by acid-labile subunit (ALS) with IGFBP-3 and pro-IGF-II was greatly decreased compared with complex formation with mature IGF-II. In contrast, ALS bound similarly to IGFBP-5 in the presence of pro-IGF-II and mature IGF-II. These studies suggest that pro-IGF-II preferentially forms binary complexes with IGFBPs, and ternary complexes with IGFBP-5, rather than ternary complexes with IGFBP-3 as seen predominantly in normal serum. This may increase the tissue availability of serum pro-IGF-II, allowing its insulin-like potential to be realised.







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