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Stability constants of aza-oxa-crown ether complexes with silver(I) in nonaqueous polar solvents

Complex formation between the silver(I) ion and monoaza- and diaza-crown ethers has been studied in five polar, nonaqueous solvents using potentiometric techniques. The stability constants are spread over seven orders of magnitude, and the major contributor to this variation is the solvation of the...

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Bibliographic Details
Published in:Inorganica Chimica Acta 2003-07, Vol.351, p.123-132
Main Authors: Thaler, A, Cox, B.G, Schneider, H
Format: Article
Language:English
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Summary:Complex formation between the silver(I) ion and monoaza- and diaza-crown ethers has been studied in five polar, nonaqueous solvents using potentiometric techniques. The stability constants are spread over seven orders of magnitude, and the major contributor to this variation is the solvation of the silver(I) cation. The ring-size dependence of the stability constants is determined both by the correspondence of the diameters of the silver(I) ion and the ring-cavity size of the macrocycles, and by specific ligand effects including association complex formation between the ligands and the solvent molecules and conformational effects in the free ligands. In the 1:1 complexes of the silver(I) ion with monoaza- and diaza-crown ethers the dominant interaction is between the silver(I) ion and the ligand's nitrogen atoms, but the ether–oxygen atoms also interact with the silver(I) ion. In the AgL 2 + complexes (L=monoaza-crown ether), however, the monoaza-crown ethers coordinate as monodentate ligands, as with simple mono-amine complexants. In these complexes the ethoxy-chains prevent direct interaction between the silver(I) cation and the solvent molecules, with the result that in dipolar aprotic solvents the free energies of transfer of the ligands and the complexes are equivalent, i.e. the so-called cryptate hypothesis holds for the AgL 2 + complexes. The complex formation between the silver(I) ion and aza-crown ethers have been studied in some polar, nonaqueous solvents. The stability constants are spread over seven orders of magnitude and are markedly influenced by the solvation of the silver(I) ion. The formation of the 1:1 inclusion complexes between diaza-crown ethers and the silver(I) ion is observed, whereas monoaza-crown ethers additionally form 1:2 (Ag +:monoaza-crown ether) complexes, in which the monoaza-crown ethers act as monodentate ligands.
ISSN:0020-1693
1873-3255
DOI:10.1016/S0020-1693(03)00193-2