Search
Ion recognition properties of new pyridine-2,6-dicarboxamide bearing propeller-like pendant residues: multi-spectroscopic approach
Abstract
The synthesis and ion binding properties of new amide derived from propeller-like tris(2-pyridyl)amine and 2,6-pyridinedicarboxylic acid chloride were described. Amide binds divalent metal cations: copper(II), nickel(II), zinc(II), and lead(II) in acetonitrile. In acetonitrile:water mixture (9:1 v/v) amide interacts only with copper(II) and nickel(II) cations forming complexes of 1:1 stoichiometry. It was found that the introduction of bulky, nitrogen donor atom bearing pendant groups can influence coordination mode of pyridine-2,6-dicarboxamides. The probable model of ligand-ion interactions is proposed on the basis of 1H NMR and FT-IR spectroscopy.
Citations
-
3
CrossRef
-
0
Web of Science
-
3
Scopus
Authors (4)
Cite as
Full text
download paper
downloaded 61 times
- Publication version
- Accepted or Published Version
- License
-
open in new tab
Keywords
Details
- Category:
- Articles
- Type:
- artykuły w czasopismach
- Published in:
-
MONATSHEFTE FUR CHEMIE
no. 151,
pages 331 - 343,
ISSN: 0026-9247 - Language:
- English
- Publication year:
- 2020
- Bibliographic description:
- Wagner-Wysiecka E., Łukasik N., Okuniewski A., Galiński B.: Ion recognition properties of new pyridine-2,6-dicarboxamide bearing propeller-like pendant residues: multi-spectroscopic approach// MONATSHEFTE FUR CHEMIE -Vol. 151, (2020), s.331-343
- DOI:
- Digital Object Identifier (open in new tab) 10.1007/s00706-020-02558-w
- Verified by:
- Gdańsk University of Technology
seen 191 times
Recommended for you
Naphthyl-vs. anthrylpyridine-2,6-dicarboxamides in cation binding studies. Synthesis and spectroscopic properties
- N. Łukasik,
- E. Wagner-Wysiecka,
- V. Hubscher-Bruder
- + 3 authors
2016