Charge-transfer complexations of 1,n-di(9-ethylcarbazol-3-yl)alkanes with tetracyanoethylene and tetranitromethane

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 71, Issue 5, 2009, Pages 1973-1978

  Asker, Erol ^a   Masnovi, John ^b  

^a BALIKESIR UNIVERSITY   (Turkey)

^b CLEVELAND STATE UNIVERSITY   (United States)

Author keywords

1,n Di(9 ethylcarbazol 3 yl)alkanes; CT complexes; Enthalpy and entropy of complexation; Tetracyanoethylene; Tetranitromethane

Indexed keywords

CHARGE TRANSFER; COMPLEXATION; CONCENTRATION (PROCESS); DICHLOROMETHANE; ENTHALPY; HYDROCARBONS; METHANE; PARAFFINS;

1,N-DI(9-ETHYLCARBAZOL-3-YL)ALKANES; ACCEPTOR COMPLEXES; CARBAZOLE GROUPS; CT COMPLEXES; DICHLOROMETHANE SOLUTIONS; ELECTRON ACCEPTORS; ELECTRON DONORS; ENTHALPIES OF FORMATIONS; FORMATION ENTHALPIES; MODEL COMPOUNDS; TEMPERATURE CHANGES; TETRACYANOETHYLENE; TETRANITROMETHANE; WEAKLY BOUND COMPLEXES;

DYES;

ALKANE; CARBAZOLE DERIVATIVE; ETHYLENE DERIVATIVE; NITRILE; TETRACYANOETHYLENE; TETRANITROMETHANE;

ABSORPTION; ARTICLE; BIOLOGICAL MODEL; CHEMICAL MODEL; CHEMISTRY; ELECTRON; ENERGY TRANSFER; MACROMOLECULE; METABOLISM; PHYSIOLOGY;

ABSORPTION; ALKANES; CARBAZOLES; ELECTRONS; ENERGY TRANSFER; ETHYLENES; MACROMOLECULAR SUBSTANCES; MODELS, BIOLOGICAL; MODELS, CHEMICAL; NITRILES; TETRANITROMETHANE;

EID: 56049115581     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2008.07.034     Document Type: Article

References (34)

1. Li D., Wang Z., Guo Z., and Lan W. Dyes Pigments 39 (1998) 133-137
2. Loh F.C., Tan K.L., and Kang E.T. Eur. Polym. J. 27 (1991) 1055-1063
3. Rocquin O., and Chevrot C. Synth. Met. 89 (1997) 119-123
4. Pielichowski J., and Sanetra J. Liet. Fiz. Rinkinys 24 (1984) 97-106
5. J. Pielichowski, J. Sanetra, Chem. Abstr. 102, 14926.
6. Wang M., Chen H.-Z., Wang J., and Yang S.-L. J. Photogr. Sci. 41 (1993) 129-130
7. C.-K. Hsiao, A.-M. Hor, G. Baranyi, H. B. Goodbrand, U.S. Patent 6,194,110 (2001).
8. Iwatsuki S., and Arai K. Makromol. Chem. 178 (1977) 2307-2319
9. M.D. Shattuck, U. Vahtra, U.S. Patent 3,484,327 (1969).
10. Law K.-Y. Chem. Rev. 93 (1993) 449-486
11. Liu Z. Chem. J. Chin. Univ. 7 (1986) 470-474
12. Z. Liu, Chem. Abstr. 106, 93513.
13. Kuczkowski A., and Zielinski R. J. Phys. D: Appl. Phys. 15 (1982) 1765-1768
14. W.J. Kukla, U.S. Patent 3,775,105 (1973).
15. K. Emoto, K. Futaki, U.S. Patent 4,387,149 (1983).
16. Sanetra J., Niziol S., and Pielichowski J. Mol. Cryst. Liq. Cryst. 353 (2000) 539-544
17. Comoretto D., Moggio I., Cuniberti C., and Dellepiane G. Synth. Met. 94 (1998) 229-234
18. P.O. Sliva, U.S. Patent 4,085,321 (1978).
19. H. Shiraishi, T. Ueno, F. Murai, H. Hayakawa, A. Isobe, U.S. Patent 5,441,849 (1995).
20. Arslan M., Masnovi J., and Krafcik R. Spectr. Acta A 64 (2006) 711-716
21. Haderski G.J., Chen Z., Krafcik R.B., Masnovi J., Baker R.J., and Towns R.L.R. J. Phys. Chem. B 104 (2000) 2242-2250
22. Sadaki S., Kham K., and Chevort C. J. Chim. Phys. 92 (1995) 819-822
23. Asker E., and Masnovi J. Acta Crystallogr. E 62 (2006) o1013-o1015
24. Online S.M., Connell L.L., Joireman P.W., Venturo V.A., and Felker P.M. Chem. Phys. Lett. 193 (1992) 335-341
25. Lynch D.E., Geissler U., Kwiatkowski J., and Whittaker A.K. Polym. Bull. 38 (1997) 493-499
26. Asker E., and Masnovi J. Acta Crystallogr. E 61 (2005) o2781-o2783
27. Park M., Buck J.R., and Rizzo C.J. Tetrahedron 54 (1998) 12707-12714
28. M. Hashimoto, M. Sasaki, T. Shimada, N. Suzuki, T. Sakai, S. Suzuka, U.S. Patent 5,260,156 (1993).
29. Liang P. Organic Syntheses vol. 3 (1955), Wiley, New York p 803 (collect.)
30. Benesi H.A., and Hildebrand J.M.J. Am. Chem. Soc. 71 (1949) 2703-2710
31. Job P. Ann. Chim. 9 (1928) 113-203
32. Levina F.A., Sidaravichyus I., Peredereeva S.I., Orlov I.G., Zaikov G.E., and Cherkashin M.I. Russ. Chem. Bull. 20 (1971) 49-52
33. Bressler D.C., Fedorak P.M., and Pickard M.A. Biotechnol. Lett. 22 (2000) 1119-1125
34. Chowdhury S., and Kebarle P.J. Am. Chem. Soc. 108 (1986) 5453-5459