Collect. Czech. Chem. Commun. 2004, 69, 2121-2133
https://doi.org/10.1135/cccc20042121

Molecular Basis of LFER. Simple Model for the Estimation of Brønsted Exponent in Acid-Base Catalysis

Robert Ponec

Institute of Chemical Process Fundamentals, Academy of Sciences of the Czech Republic, Rozvojová 135, 165 02 Prague 6, Czech Republic

References

1. Brønsted J. N., Pedersen K. J.: Z. Phys. Chem. 1924, 108, 185.
2. Bell R. P.: Proc. R. Soc. A 1936, 154, 414. <https://doi.org/10.1098/rspa.1936.0060>
3. Horiuti J., Polanyi M.: Acta Physicochim. URSS 1935, 2, 505.
4. Marcus R. A.: J. Phys. Chem. 1968, 72, 891. <https://doi.org/10.1021/j100849a019>
5. Marcus R. A.: J. Am. Chem. Soc. 1969, 91, 7224. <https://doi.org/10.1021/ja01054a003>
6. Levich V. G., Dogonadze R. R., German E. D., Kuznetsov A. M., Kharkats Yu. I.: Electrochim. Acta 1970, 15, 353. <https://doi.org/10.1016/0013-4686(70)80027-5>
7. Koeppl G. V., Kresge A. J.: J. Chem. Soc., Chem. Commun. 1973, 371. <https://doi.org/10.1039/c39730000371>
8. Bell R. P.: J. Chem. Soc., Faraday Trans. 2 1976, 2088. <https://doi.org/10.1039/f29767202088>
9. Murdoch R. R.: J. Am. Chem. Soc. 1972, 94, 4410. <https://doi.org/10.1021/ja00768a002>
10. Cohen A. O., Marcus R. A.: J. Phys. Chem. 1968, 72, 4249. <https://doi.org/10.1021/j100858a052>
11. Bell R. P.: The Proton in Chemistry, Chap. 10. Cornell University Press, New York 1959.
12. Lefler J. E., Grunwald E.: Rates and Equilibria of Organic Reactions, Chap. 7. Dover Publications Inc., New York 1989.
13. Eigen M.: Angew. Chem., Int. Ed. Engl. 1964, 3, 1. <https://doi.org/10.1002/anie.196400011>
14. Kresge A. J.: Chem. Soc. Rev. 1973, 2, 475. <https://doi.org/10.1039/cs9730200475>
15. Lewis E. S., Shen C. C., More O’Ferral R.: J. Chem. Soc., Perkin Trans. 2 1981, 1084. <https://doi.org/10.1039/p29810001084>
16. Tupitsin I. F.: Russ. J. Gen. Chem. 2004, 74, 179. <https://doi.org/10.1023/B:RUGC.0000025497.22963.5d>
17. Bell R. P., Gelles E., Møller E.: Proc. R. Soc. A 1940, 198, 308. <https://doi.org/10.1098/rspa.1949.0103>
18. Bell R. P., Goldsmith H. L.: Proc. R. Soc. A 1951, 210, 322. <https://doi.org/10.1098/rspa.1952.0003>
19. Bell R. P., Lidwell D. M.: Proc. R. Soc. A 1940, 176, 88. <https://doi.org/10.1098/rspa.1940.0080>
20. March J.: Advanced Organic Chemistry. Reactions, Mechanisms and Structure. J. Wiley & Sons, New York 1985.
21. Guthrie J. P.: J. Phys. Org. Chem. 1998, 11, 632. <https://doi.org/10.1002/(SICI)1099-1395(199808/09)11:8/9<632::AID-POC47>3.0.CO;2-1>
22. Pedersen K. J.: K. Danske Vidensk. Selsk. Skr. Mat.-Fys. Medd. 1932, 12, 1.
23. Bell R. P., Goodall D. M.: Proc. R. Soc. A 1966, 294, 273. <https://doi.org/10.1098/rspa.1966.0207>
24. Maron S. H., La Mer V. K.: J. Am. Chem. Soc. 1939, 61, 2018. <https://doi.org/10.1021/ja01877a020>
25. Pearson R. G.: J. Am. Chem. Soc. 1948, 70, 204. <https://doi.org/10.1021/ja01181a058>
26. Pearson R. G., Dilton R. L.: J. Am. Chem. Soc. 1953, 75, 2439. <https://doi.org/10.1021/ja01106a048>
27. Pearson R. G., Williams F. V.: J. Am. Chem. Soc. 1954, 76, 258. <https://doi.org/10.1021/ja01630a066>
28. Pearson R. G., Williams F. V.: J. Am. Chem. Soc. 1953, 75, 3073. <https://doi.org/10.1021/ja01109a008>
29. Grerory M. J., Bruice M. T.: J. Am. Chem. Soc. 1967, 89, 3227.
30. Belikov V. M., Korchemnaya Ts. B., Faleev N. G.: Izv. Akad. Nauk SSSR, Ser. Khim. 1969, 1383.
31. Bordwell F. G., Boyle W. J., Jr., Hautala J. A., Yee K. C.: J. Am. Chem. Soc. 1969, 91, 4002. <https://doi.org/10.1021/ja01042a082>
32. Kresge A. J.: J. Am. Chem. Soc. 1970, 92, 3210. <https://doi.org/10.1021/ja00713a062>
33. Bordwell F. G., Boyle W. J., Jr., Yee K. C.: J. Am. Chem. Soc. 1970, 92, 5926. <https://doi.org/10.1021/ja00723a019>
34. Bordwell F. G., Boyle W. J., Jr.: J. Am. Chem. Soc. 1972, 94, 3907. <https://doi.org/10.1021/ja00766a041>
35. Fukuyama M., Flanagan P. W. K., Williams F. T., Jr., Frainier L., Miller S. A., Shechter H.: J. Am. Chem. Soc. 1970, 92, 4689. <https://doi.org/10.1021/ja00718a036>
36. Hammond G. S.: J. Am. Chem. Soc. 1955, 77, 334. <https://doi.org/10.1021/ja01607a027>