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Anion binding by p-aminoazobenzene-derived aromatic amides: spectroscopic and electrochemical studies
Abstract
The synthesis and complexing properties of p-aminoazobenzene-derived mono-, bis-, and trisamides were described. Ligands 3 and 4 bind anions, including fluorides, chlorides, bromides, acetates, benzoates, dihydrogen phosphates, hydrogen sulfates, and p-toluenesulfonates, in chloroform forming 1 : 1 complexes. The highest value of stability constant was evaluated for the 4-F− complex (log K = 5.63 ± 0.21). On the basis of 1H NMR, and FTIR spectroscopy, the possible nature of the ligand–anion interactions was proposed. The E ⇄ Z isomerization process of tripodal amide 4 in chloroform was studied. The effect of anions on Z to E thermal back isomerization was investigated.
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- Accepted or Published Version
- DOI:
- Digital Object Identifier (open in new tab) 10.1039/c7pp00245a
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- Copyright (2017 The Royal Society of Chemistry and Owner Societies)
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- Category:
- Articles
- Type:
- artykuł w czasopiśmie wyróżnionym w JCR
- Published in:
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PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
no. 16,
pages 1570 - 1579,
ISSN: 1474-905X - Language:
- English
- Publication year:
- 2017
- Bibliographic description:
- Łukasik N., Wagner-Wysiecka E.: Anion binding by p-aminoazobenzene-derived aromatic amides: spectroscopic and electrochemical studies// PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES. -Vol. 16, iss. 10 (2017), s.1570-1579
- DOI:
- Digital Object Identifier (open in new tab) 10.1039/c7pp00245a
- Verified by:
- Gdańsk University of Technology
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