Synthesis and properties of azobenzocrown ethers with π-electron donor, or π-electron donor and π-electron acceptor group(s) on benzene ring(s)

Tetrahedron

Volumn 61, Issue 45, 2005, Pages 10738-10747

  Luboch, Elzbieta ^a   Wagner Wysiecka, Ewa ^a   Poleska Muchlado, Zuzanna ^a   Kravtsov, Victor Ch ^b  

^a GDANSK UNIVERSITY OF TECHNOLOGY   (Poland)

^b INSTITUTE OF APPLIED PHYSICS   (Moldova)

Author keywords

Azo compounds; Chromoionophores; Macrocyclic ligands; Synthetic methods; UV vis spectroscopy

Indexed keywords

4 DIMETHYLAMINO 4' NITROAZOBENZENE; AZOBENZENE DERIVATIVE; BENZENE; CROWN ETHER DERIVATIVE; FUNCTIONAL GROUP; METAL ION; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CRYSTAL STRUCTURE; ELECTRON; PRIORITY JOURNAL; SUBSTITUTION REACTION; SYNTHESIS; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 26244444513     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.08.071     Document Type: Article

References (24)

1. For example see review: E. Luboch, R. Bilewicz, M. Kowalczyk, E. Wagner-Wysiecka, and J.F. Biernat Azo Macrocyclic Compounds G.W. Gokel Advances in Supramolecular Chemistry Vol. 9 2003 Cerberus South Miami, USA 71
2. M. Shiga, M. Takagi, and K. Ueno Chem. Lett. 1980 1021
3. M. Shiga, H. Nakamura, M. Tagaki, and K. Ueno Bull. Chem. Soc. Jpn. 57 1984 412
4. E. Luboch, and A. Biedrzycka Pol. J. Chem. 77 2003 47
5. J.F. Biernat, E. Luboch, A. Cygan, Yu.A. Simonov, A.A. Dvorkin, E. Muszalska, and R. Bilewicz Tetrahedron 48 1992 4399
6. E. Luboch, J.F. Biernat, E. Muszalska, and R. Bilewicz Supramol. Chem. 5 1995 201
7. E. Luboch, J.F. Biernat, Yu.A. Simonov, and A.A. Dvorkin Tetrahedron 54 1998 4977
8. D.G. Pijanowska, E. Luboch, J.F. Biernat, M. Dawgul, and W. Torbicz Sens. Actuators, B 58 1999 384
9. For example see: (a) H. Huesmann, J. Maack, D. Möbius, and J.B. Biernat Sens. Actuators, B 29 1995 148
10. E. Muszalska, and R. Bilewicz Analyst 119 1994 1235
11. E. Muszalska, R. Bilewicz, E. Luboch, A. Skwierawska, and J.F. Biernat J. Inclusion Phenom. 26 1996 47
12. I. Zawisza, R. Bilewicz, E. Luboch, and J.F. Biernat J. Chem. Soc., Dalton Trans. 2000 499
13. R. Tahara, T. Morozumi, H. Nakamura, and M. Shimomura J. Phys. Chem. B 101 1997 7736
14. E. Luboch, E. Wagner-Wysiecka, and J.F. Biernat J. Supramol. Chem. 2 2002 279
15. E. Hofer, and H. Uffman Tetrahedron Lett. 1971 3241
16. E. Chapoteau, B.P. Czech, C.R. Gebauer, A. Kumar, K. Leong, D. Mytych, W. Zazulak, D.H. Desai, E. Luboch, J. Krzykawski, and R.A. Bartsch J. Org. Chem. 56 1991 2575
17. E. Luboch, and V.Ch. Kravtsov J. Mol. Struct. 699 2004 9
18. J. Dale Acta Chem. Scand. 27 1973 1115
19. C.J. Pedersen J. Am. Chem. Soc. 89 1967 2945
20. D. Mootz, A. Albert, S. Schaefgen, and D. Stäben J. Am. Chem. Soc. 116 1994 12045
21. S. Krongsuk, T. Kerdcharoen, and S. Hannongbua J. Phys. Chem. B 107 2003 4175
22. M. Ouchi, Y. Inoue, Y. Liu, S. Nagamune, S. Nakamura, K. Wada, and T. Hakushi Bull. Chem. Soc. Jpn. 63 1990 1260
23. Sheldrik, G. M. SHELX-97: Programs for the solution and refinement of crystal structures; University of Gottingen: Gottingen, Germany, 1997.
24. P. Kuzmič Anal. Biochem. 237 1996 260 http://www.biokin.com