Collect. Czech. Chem. Commun.
2006, 71, 1359-1370
https://doi.org/10.1135/cccc20061359
Charge Transfer Molecular Complexes of 4-(Dimethylamino)pyridine with Some Conventional and Unconventional Acceptors Involving Fluoroarenes
Usama M. Rabie
Chemistry Department, Faculty of Science at Qena, South Valley University, Qena 83523, Egypt
References
1. Science 1993, 259, 194.
< A. R., Solomon S., Turnipseed A. A., Warren R. F.: https://doi.org/10.1126/science.259.5092.194>
2. Nature 1974, 249, 810.
< M. J., Rowland F. S.: https://doi.org/10.1038/249810a0>
3. Anderson R. F., Punderson J. O. in: Organofluorine Chemicals and Their Industrial Applications (R. E. Banks, Ed.). Ellis Horwood, Chichester 1979.
4. Chambers R. D.: Fluorine in Organic Chemistry. Wiley, New York 1973.
5. Banks R. E., Smart B. E., Tatlow J. C.: Organofluorine Chemistry. Principles and Commercial Applications. Plenum Press, New York 1994.
6. J. Chem. Soc. B 1967, 1131.
< T. G., Davis K. M. C.: https://doi.org/10.1039/j29670001131>
7. J. Phys. Chem. 1965, 69, 2153.
< J. C. A., Herbstein F. H.: https://doi.org/10.1021/j100891a003>
8. Indian J. Chem., Sect. A: Inorg., Phys., Theor. Anal. 1984, 23, 543.
F., Jain D. V. S.:
9. Acta Chem. Scand. 1989, 43, 172.
< T.: https://doi.org/10.3891/acta.chem.scand.43-0172>
10. J. Chem. Soc. B 1967, 406.
< N. M. D., Foster R., Fyfe C. A.: https://doi.org/10.1039/j29670000406>
11. J. Org. Chem. 1988, 53, 537.
< L. J., Keefer R. M.: https://doi.org/10.1021/jo00238a012>
12. Spectrochim. Acta, Part A 1987, 43, 11.
< A. E.: https://doi.org/10.1016/0584-8539(87)80193-9>
13. Bull. Chem. Soc. Jpn. 1993, 66, 3171.
< M.: https://doi.org/10.1246/bcsj.66.3171>
14. J. Fluorine Chem. 1998, 91, 49.
< J., Sanford M., Crabtree R. H.: https://doi.org/10.1016/S0022-1139(98)00215-2>
15. Bull. Soc. Chim. Fr. 1997, 134, 955.
J., Crabtree R. H., Rheingold A. L., Yap G. P. A.:
16. Inorg. Chim. Acta 1998, 270, 559.
< C. M., Burdeniuc J., Crabtree R. H., Rheingold A. L., Yap G. P. A.: https://doi.org/10.1016/S0020-1693(97)05999-9>
17. Spectrochim. Acta, Part A 1987, 43, 711.
< E., Matsumura S., Imai Y., Aida K.: https://doi.org/10.1016/0584-8539(87)80157-5>
18. J. Phys. Chem. 1972, 76, 1895.
< J. M., Sonnessa A. J.: https://doi.org/10.1021/j100657a020>
19. J. Org. Chem. 2000, 65, 3154.
< A. C., Fekner T., Spey S. E.: https://doi.org/10.1021/jo0000574>
20. J. Am. Chem. Soc. 1997, 119, 1492.
< J. C., Latham H. A., Fu C. G.: https://doi.org/10.1021/ja963835b>
21. J. Org. Chem. 1998, 63, 2794.
< J. C., Tweddell J., Fu C. G.: https://doi.org/10.1021/jo980183w>
22. J. Am. Chem. Soc. 1999, 121, 5091.
< B., Ruble J. C., Hoic D. A., Fu C. G.: https://doi.org/10.1021/ja9906958>
23. Bull. Chem. Soc. Jpn. 2004, 77, 681.
< U. M., Salman H. M. A., Abou-El-Wafa M. H. M.: https://doi.org/10.1246/bcsj.77.681>
24. Inorg. Chem. 1997, 36, 2236.
< U. M., Patel B. P., Crabtree R. H., Mahmoud M. R.: https://doi.org/10.1021/ic961361b>
25. J. Phys. Chem. 1964, 41, 1609.
< Y.: https://doi.org/10.1063/1.1726131>
26. J. Am. Chem. Soc. 1966, 88, 3216.
< S. N., Rao C. N. R.: https://doi.org/10.1021/ja00966a008>
27. J. Org. Chem. 1966, 31, 1214.
< R. L., Osiecki J. H., Ottenberg A.: https://doi.org/10.1021/jo01342a055>
28. J. Indian Chem. Soc. 1983, 60, 842.
B., Varshney A., Bhat S. N.:
29. Helv. Chim. Acta 1983, 66, 1110.
< P., Joly D.: https://doi.org/10.1002/hlca.19830660414>
30. J. Am. Chem. Soc. 1986, 108, 4459.
< J. S., Krusic P. J., Dixon D. A., Reiff W. M., Zhang J. H., Anderson E. C., Epstein A. J.: https://doi.org/10.1021/ja00275a036>
31. Can. J. Anal. Spectrosc. 2002, 49, 1.
H. M. A., Rabie U. M., Abd-Alla E. M.:
32. Inorg. Chem. Commun. 2004, 7, 1209.
< H. M. A., Mahmoud M. R., Abou-El-Wafa M. H. M., Rabie U. M., Crabtree R. H.: https://doi.org/10.1016/j.inoche.2004.07.023>
33. J. Am. Chem. Soc. 1949, 71, 2703.
< H. A., Hildebrand J. H.: https://doi.org/10.1021/ja01176a030>
34. Rec. Trav. Chim. Pays-Bas 1956, 75, 787.
< R. L.: https://doi.org/10.1002/recl.19560750711>
35. Can. J. Appl. Spectrosc. 1994, 39, 24.
M. M. A., Abdalla E. M., Mahmoud M. R.:
36. Spectrochim. Acta, Part A 1990, 46, 1107.
< N. S., Rao G. B.: https://doi.org/10.1016/0584-8539(90)80229-R>
37. J. Inclusion Phenom. Macromol. Chem. 2004, 48, 135.
< M., Shamsipur M.: https://doi.org/10.1023/B:JIPH.0000022520.53138.f4>
38. Albert A. in: Physical Methods in Heterocyclic Chemistry (A. R. Katritzky, Ed.), Vol. 1. Academic Press, New York 1963.
39. J. Phys. Chem. 1970, 74, 2299.
< A., Testa A. C.: https://doi.org/10.1021/j100705a010>
40. Lambert J. B., Shurvell H. F., Lightner D. A., Cooks R. G.: Introduction to Organic Spectroscopy. Macmillan Publishing Company, New York 1987.
41. J. Am. Chem. Soc. 1982, 104, 4403.
< E., Reis A. H., Jr., Miller J. S., Rommelmann H., Epstein A. J.: https://doi.org/10.1021/ja00380a015>
42. J. Am. Chem. Soc. 1982, 38, 1225.
G., Pra A. D.:
43. Bull. Soc. Chim. Fr. 1990, 127, 485.
S. A., El-Nady A. M., Salman H. M. A.:
44. Spectrochim. Acta 1988, 44, 1185.
< M. M., Hamed M. M. A., Salman H. M. A.: https://doi.org/10.1016/0584-8539(88)80090-4>
45. Spectrosc. Lett. 1995, 28, 29.
< M. M. A., Bakr M., Mahmoud M. R.: https://doi.org/10.1080/00387019508011652>
46. Bull. Chem. Soc. Jpn. 1971, 44, 2615.
Y.:
47. Bull. Chem. Soc. Jpn. 1967, 40, 231.
< Y., Matsunga Y.: https://doi.org/10.1246/bcsj.40.231>
48. Chem. Rev. 1988, 88, 201.
< J. S., Epstein A. J., Reiff W. M.: https://doi.org/10.1021/cr00083a010>
49. J. Org. Chem. 1997, 62, 4687.
< I., Rozas I., Elguero J.: https://doi.org/10.1021/jo970125v>
50. Lide D. R.: Handbook of Chemistry and Physics, 77th ed. CRC Press, New York 1996–1997.
51. Chem. Commun. 1965, 642.
R., Fyfe C. A.:
52. Foster R.: Organic Charge-Transfer Complexes. Academic Press, London 1969.