Naphthyl-vs. anthrylpyridine-2,6-dicarboxamides in cation binding studies. Synthesis and spectroscopic properties
Abstract
Pyridine-2,6-carboxamides bearing - or -naphthyl- and - or -anthryl- residues were prepared using simple method from pyridine-2,6-carboxylic acid dichloride and the respective aromatic amines. For the obtained receptors selective binding of lead(II), and copper(II) was found. Ion-receptor interactions were studied using UV-vis spectroscopy, spectrofluorimetry, 1H NMR, and FTIR spectroscopy. The reversible lead(II) and copper(II) binding was discussed in regard of type of aromatic residue and amide bond localization in aromatic ring and binding model was proposed.
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- DOI:
- Digital Object Identifier (open in new tab) 10.1080/10610278.2015.1119830
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- Category:
- Articles
- Type:
- artykuł w czasopiśmie wyróżnionym w JCR
- Published in:
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SUPRAMOLECULAR CHEMISTRY
no. 28,
edition 7-8,
pages 673 - 685,
ISSN: 1061-0278 - Language:
- English
- Publication year:
- 2016
- Bibliographic description:
- Łukasik N., Wagner-Wysiecka E., Hubscher-Bruder V., Michel s., Bocheńska M., Kamińska B.: Naphthyl-vs. anthrylpyridine-2,6-dicarboxamides in cation binding studies. Synthesis and spectroscopic properties// SUPRAMOLECULAR CHEMISTRY. -Vol. 28, iss. 7-8 (2016), s.673-685
- DOI:
- Digital Object Identifier (open in new tab) 10.1080/10610278.2015.1119830
- Verified by:
- Gdańsk University of Technology
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