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Do Phenyl Substituents Affect the Properties of Azobenzocrown Derivatives?

Abstract

New products of photo- and thermal rearrangements of 19-membered azoxybenzocrown with phenyl substituents in benzene rings in the para positions to oligooxyethylene fragments are characterized. The yields of photochemical transformations depend on the solvent. Para-hydroxyazocrown is formed with yields over 50% in propan-2-ol. Ortho-hydroxyazobenzocrown is obtained with yields up to 70% in toluene/acetic acid mixture. Macrocyclic Ph-20-ester is obtained in yield 90% under thermochemical rearrangement conditions. Structure of new hydroxyazobenzocrowns and also atypical product of rearrangements, 20-membered ester, was confirmed by X-ray diffraction analysis. Azophenol⇄quinone–hydrazone tautomeric equilibrium of new hydroxyazobenzocrowns and the influence of metal cations on tautomeric equilibrium was investigated using 1H NMR and UV-Vis spectroscopy in acetonitrile. The highest value of stability constant (logK 7.25) was obtained for strontium complex of p-hydroxyazobenzocrown. For the first time p-hydroxyazobenzocrown was used as a chromoionophore in the receptor layer of an optical sensor. Comparative analysis with data obtained previously for series 19-membered analogs have shown the influence of the presence of substituents in benzene rings for the course and products distribution of photo- and thermal rearrangement. The effect of substituents was also discussed against the tautomeric equilibrium and metal cation complexation properties.

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DOI:
Digital Object Identifier (open in new tab) 10.1002/cplu.202300175
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Copyright (2023 Wiley-VCH GmbH)

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Category:
Articles
Type:
artykuły w czasopismach
Published in:
ChemPlusChem no. 88, pages 1 - 18,
ISSN: 2192-6506
Language:
English
Publication year:
2023
Bibliographic description:
Wagner-Wysiecka E., Szulc P., Luboch E., Chojnacki J., Laskowska D., Miklaszewska P., Sowiński P.: Do Phenyl Substituents Affect the Properties of Azobenzocrown Derivatives?// ChemPlusChem -Vol. 88,iss. 6 (2023), s.1-18
DOI:
Digital Object Identifier (open in new tab) 10.1002/cplu.202300175
Sources of funding:
  • Free publication
Verified by:
Gdańsk University of Technology

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