Synthesis and Application of Chelated Complexes [Zn(Z-arg)2(H2O)] and [[Zn(Z-arg)2(H2O)](SO4)]2- as Chiral Selectors

By interaction of compounds Zn(II) and L-arginine (L-Arg) the chelated complexes [Zn(L-arg)2(H2O)] (I) and [[Zn(L-arg)2(H2O)](SO4)]2- (II) (L-arg is a deprotonated form of L-Arg) were synthesized. The structure of the obtained complexes was established by IR spectroscopy by comparing the experimental and theoretical IR spectra using quantum chemical modeling. Complexes I and II were studied as chiral selectors of enantioselective voltammetric sensors. It was shown that I exhibits better enantioselective compared to II. By DFT method, it was found that the difference in the exhibited enantioselectivity of complexes I and II can be due of the geometric isomerism of chelate compounds and the peculiarities of the coordination of the obtained complexes with the analyte molecule.

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Publication Details

Journal
Координационная химия / Russian Journal of Coordination Chemistry
Published
2025-01-01
DOI
https://doi.org/10.7868/s3034549925050042
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
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article

Synthesis and Application of Chelated Complexes [Zn(Z-arg)2(H2O)] and [[Zn(Z-arg)2(H2O)](SO4)]2- as Chiral Selectors

Т. В. Берестова
Координационная химия / Russian Journal of Coordination Chemistry
Lanthanide and Transition Metal Complexes
article

Synthesis and Application of Chelated Complexes [Zn(Z-arg)2(H2O)] and [[Zn(Z-arg)2(H2O)](SO4)]2- as Chiral Selectors

Т. В. Берестова
article en

Abstract

By interaction of compounds Zn(II) and L-arginine (L-Arg) the chelated complexes [Zn(L-arg)2(H2O)] (I) and [[Zn(L-arg)2(H2O)](SO4)]2- (II) (L-arg is a deprotonated form of L-Arg) were synthesized. The structure of the obtained complexes was established by IR spectroscopy by comparing the experimental and theoretical IR spectra using quantum chemical modeling. Complexes I and II were studied as chiral selectors of enantioselective voltammetric sensors. It was shown that I exhibits better enantioselective compared to II. By DFT method, it was found that the difference in the exhibited enantioselectivity of complexes I and II can be due of the geometric isomerism of chelate compounds and the peculiarities of the coordination of the obtained complexes with the analyte molecule.

Координационная химия / Russian Journal of Coordination ChemistryVol. 51(5)
Openalex Percentile: Top 79%
Lanthanide and Transition Metal Complexes
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