Molar absorption coefficients and stability constants of Zincon metal complexes for determination of metal ions and bioinorganic applications.

Abstract:

:Zincon (ZI) is one of the most common chromophoric chelating probes for the determination of Zn2+ and Cu2+ ions. It is also known to bind other metal ions. However, literature data on its binding properties and molar absorption coefficients are rather poor, varying among publications or determined only in certain conditions. There are no systematic studies on Zn2+ and Cu2+ affinities towards ZI performed under various conditions. However, this widely commercially available and inexpensive agent is frequently the first choice probe for the measurement of metal binding and release as well as determination of affinity constants of other ligands/macromolecules of interest. Here, we establish the spectral properties and the stability of ZI and its complexes with Zn2+, Cu2+, Cd2+, Hg2+, Co2+, Ni2+ and Pb2+ at multiple pH values from 6 to 9.9. The obtained results show that in water solution the MZI complex is predominant, but in the case of Co2+ and Ni2+, M(ZI)2 complexes are also formed. The molar absorption coefficient at 618 nm for ZnZI and 599nm for CuZI complexes at pH7.4 in buffered (I=0.1M) water solutions are 24,200 and 26,100M-1cm-1, respectively. Dissociation constants of those complexes are 2.09×10-6 and 4.68×10-17M. We also characterized the metal-assisted Zincon decomposition. Our results provide new and reassessed optical and stability data that are applicable to a wide range of chemical and bioinorganic applications including metal ion detection, and quantification and affinity studies of ligands of interest. SYNOPSIS:Accurate values of molar absorption coefficients of Zincon complex with Zn2+, Cd2+, Hg2+, Co2+, Ni2+, Cu2+, and Pb2+ for rapid metal ion quantification are provided. Zincon stability constants with Zn2+ and Cu2+ in a wide pH range were determined.

journal_name

J Inorg Biochem

authors

Kocyła A,Pomorski A,Krężel A

doi

10.1016/j.jinorgbio.2017.08.006

subject

Has Abstract

pub_date

2017-11-01 00:00:00

pages

53-65

eissn

0162-0134

issn

1873-3344

pii

S0162-0134(17)30387-2

journal_volume

176

pub_type

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