Toward a quantitative evaluation of Lewis acid strength. A 13C NMR study of the interaction of boron trifluoride with diethyl ether

Journal of Molecular Catalysis A: Chemical

Volumn 137, Issue 1-3, 1999, Pages 213-221

  Fǎrcaşiu, Dan ^a   Lukinskas, Povilas ^a   Ghenciu, Anca ^a   Martin, Rebecca ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

13C dynamic NMR spectroscopy; Boron trifluoride; Diethyl ether; Lewis acid strengths

Indexed keywords

BORON TRIFLUORIDE DIETHYL ETHERATE; DICHLOROMETHANE; ETHER; UNCLASSIFIED DRUG;

ACID BASE BALANCE; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; DECOMPOSITION; ENTHALPY; MOLECULAR INTERACTION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; QUANTITATIVE DIAGNOSIS;

EID: 0344835861     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1381-1169(98)00127-7     Document Type: Article

References (53)

1. Parry E.P. J. Catal. 2:1963;371.
2. H. Knözinger, in: D.D. Eley, H. Pines, P.B. Weisz (Eds.), Advances in Catalysis, Vol. 25, Academic Press, London, 1976, p. 184.
3. Paukshtis E.A., Yurchenko E.A. Usp. Khim. 52:1983;426.
4. Pelmenschikov A.G., van Santen R.A., Jänchen J., Meijer E. J. Phys. Chem. 97:1993;11071.
5. Adeeva V., de Haan J.W., Jänchen J., Lei G.D., Schünemann V., van de Ven L.J.M., Sachtler W.M.H., van Santen R.A. J. Catal. 151:1995;364.
6. Tábora J.E., Davis R.J. J.C.S. Faraday Trans. 91:1995;1825.
7. Yamaguchi T., Tanabe K., Kung Y.C. Mater. Chem. Phys. 16:1986;67.
8. Pinna F., Signoretto M., Strukul G., Cerrato G., Morterra C. Catal. Lett. 26:1994;339.
9. Comelli R.A., Vera C.R., Parera J.M. J. Catal. 151:1995;96.
10. Nascimento P., Akratopoulou C., Oszagyan M., Coudurier G., Travers C., Joly J.F., Védrine J.C. Stud. Surf. Sci. Catal. 75:1993;1185.
11. Morterra C., Cerrato G., Emanuel C., Bolis V. J. Catal. 142:1993;349.
12. Kustov L.M., Kazansky V.B., Figueras F., Tichit D. J. Catal. 150:1994;143.
13. Bensitel M., Saur O., Lavalley J.C., Mabilon G. Mater. Chem. Phys. 17:1987;249.
14. Escalona-Platero E., Peñarroya Mentruit M. Catal. Lett. 30:1995;31.
15. Morterra C., Cerrato G., Pinna F., Signoretto M., Strukul G. J. Catal. 149:1994;181.
16. Waqif M., Bachelier J., Saur O., Lavalley J.-C. J. Mol. Catal. 72:1992;127.
17. K. Tanabe, M. Itoh, K. Morishige, H. Hattori, in: B. Delmon, P.A. Jacobs, G. Poncelet (Eds.), Preparation of Catalyst, Elsevier, Amsterdam, 1976, p. 65.
18. M. Hino, K. Arata, J.C.S. Chem. Commun. (1979) 1148.
19. K. Ebitani, J. Konishi, A. Horie, H. Hattori, K. Tanabe, Proc. Intl. Symp. Acid-Base Catal., Sapporo, 1988, p. 491.
20. Ebitani K., Konishi J., Hattori H. J. Catal. 130:1991;257.
21. Ebitani K., Tsuji J., Hattori H., Kita H. J. Catal. 135:1992;609.
22. Zhang C., Miranda R., Davis B.H. Catal. Lett. 29:1994;349.
23. Ebitani K., Konno H., Tanaka T., Hattori H. J. Catal. 135:1992;60.
24. Fǎrcaşiu D., Ghenciu A. Progr. NMR Spectroscopy. 29:1996;129. and references therein.
25. G.A. Olah, G.K. Surya Prakash, J. Sommer, Superacids, Wiley-Interscience, New York, 1985, pp. 24-25.
26. Gutmann V. Coord. Chem. Rev. 2:1967;239.
27. V. Gutmann, The Donor-Acceptor Approach to Molecular Interactions, Plenum, New York, 1978.
28. Mayer U., Gutmann V., Gerger W. Monatsh. Chem., 106:1975;1235.
29. Christian Reichardt, Solvents and Solvent Effects in Organic Chemistry, 2nd edn., VCH, Weinheim, 1988.
30. Drago R.S., Wayland B.B. J. Am. Chem. Soc. 87:1965;3571.
31. Drago R.S., Parr L.B., Chamberlain C.S. J. Am. Chem. Soc. 99:1977;3203.
32. D. Fǎrcaşiu, M. Stan, J. Chem. Soc. Perkins Trans. 2 (1988) in print.
33. Fǎrcaşiu D., Ghenciu A. J. Am. Chem. Soc. 115:1993;10901.
34. D.S. Stephenson, G. Binsch, program QCPE 569 (modified by C.B. LeMaster, C.L. LeMaster, N.S. True), QCPE, Indiana University.
35. Binsch G. J. Am. Chem. Soc. 91:1969;1304.
36. D.F. DeTar, in: D.F. DeTar (Ed.), Computer Programs for Chemists, W.A. Benjamin, New York, 1968, Vol. 1, pp. 126-173.
37. Modified by: W.F. Sliwinski, PhD Thesis, Princeton University, 1972.
38. Gasselin V. Ann. Chim. 7:1894;5.
39. Brown H.C., Adams R.M. J. Am. Chem. Soc. 64:1942;2557.
40. Laubengayer A.W., Finlay G.R. J. Am. Chem. Soc. 65:1943;84.
41. Maria P.C., Gal J.-F. J. Phys. Chem. 89:1985;1296.
42. Bukka K., Satchell R.S. J. Chem. Soc. Perkins Trans. 2:1976;1058.
43. Coyle T.D., Stone F.G.A. J. Am. Chem. Soc. 83:1961;4138.
44. Craig R.A., Richards R.E. Trans. Faraday Soc. 59:1963;1962.
45. Gore E., Danyluk S.S. J. Phys. Chem. 69:1965;89.
46. Deters J.F., McCusker P.A., Pilger R.C. Jr. J. Am. Chem. Soc. 90:1968;4583.
47. Satchell R.S., Bukka K., Payne C.J. J. Chem. Soc. Perkins Trans. 2:1975;541.
48. Brownstein S., Eastham A.M., Latremouille G.A. J. Phys. Chem. 67:1963;1028.
49. Rutenberg A.C., Palko A.A., Drury J.S. J. Am. Chem. Soc., 85:1963;2702.
50. Fratiello A., Onak T.P., Schuster R.E. J. Am. Chem. Soc. 90:1968;1194.
51. Rutenberg A.C., Palko A.A., Drury J.S. J. Phys. Chem. 68:1964;976.
52. E.D. Hughes, J. Chem. Soc. (1935) 255.
53. Kogelbauer A., Reddick J., Fǎrcaşiu D. J. Mol. Catal. 103:1995;31.