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W poszukiwaniu idealnego chromojonofora

Zarzeczańska Dorota, Wcisło Anna, Smułka Agata, Ossowski Tadeusz

Wiadomości Chemiczne

2022

[Z] 76, 7-8

663--676

In pursuit for new chromoionophores, it is important to know their functioning, which depends primarily on theirstructure. The structures of chromoionophores were discussed, highlighting the elements that have a significant impact on their operation, i.e. the binding and visualization of metal ion binding. Chromoionophores are composed of a binding and signaling group. Valinomycin, salinomycin and synthetic crown ethers are presented as ionophores. Using the anthraquinone as an example, the function of the chromophore system was defined and discussed. It has been shown that an element connecting the main components of the chromoionophore may also play an important role. The action of chromoionophores is directly related to their acid-base properties, which can influence both ion binding and the visualization of interactions. The examples of aminoanthraquinone derivatives show the influence of the number of groups, position in the anthraquinone ring and the order of amino groups on the basicity of chromoionophores.

Optical recognition elements. Macrocyclic imidazole chromoionophores entrapped in silica xerogel

Kledzik K., Jamrógiewicz M., Gwiazda M., Wagner-Wysiecka E., Jezierska J., Biernat J. F., Kłonkowski A. M.

Materials Science Poland

2007

Vol. 25, No. 4

1041--1051

Materials containing new chromoionophores consisting of crown residue and azole moiety as parts of macrocycles were encapsulated by the sol-gel procedure in silica xerogel matrices and proposed as chemical recognition elements especially for such metal ions as Li+, Cs+ and Cu2+. Action of these recognition elements is in principle based on changes of reflectance. The recognition elements containing 21- membered chromogenic derivatives of unsubstituted imidazole and 4-methylimidazole are able to distinguish in aqueous solution whether the Li+ concentration ratio is lower or higher than 1. In the case of Cu2+ complexes with 18-membered macrocyclic chromoionophore in which phenol residue was replaced by imidazole and 21-membered chromogenic derivative of 4-methylimidazole, values of the EPR parameters g and A suggest participation of two oxygen and two nitrogen atoms of the ligand in the equatorial plane of the tetragonally distorted octahedral environment of the central ion.