A comparison of sensitivities to substituent effects of five-membered heteroaromatic rings in gas phase ionization

Journal of the Chemical Society B: Physical Organic

Volumn , Issue , 1971, Pages 1585-1587

  Linda, Paolo ^a   Marino, Gianlorenzo ^a   Pignataro, Salvatore ^b  

^a UNIVERSITY OF PERUGIA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 37049134085     PISSN: 00456470     EISSN: None     Source Type: Journal    
DOI: 10.1039/J29710001585     Document Type: Review

References (36)

1. Preliminary communication on the ionization potentials of 2-substituted thiophens, S. Pignataro, P. Linda, and G. Marino, Ricerca sci., 1969, 39, 668.
2. F. Fringuelli, G. Marino, and G. Savelli, Tetrahedron, 1969, 25, 5815.
3. T. A. Melent’eva, L. V. Kazanskaya, and V. M. Berezovskii, Doklady Akad. Nauk S.S.S.R., 1967, 175, 354 (Chem. Abs., 1967, 67, 120,484).
4. J. Tirouflet, Adv. Polarography, 1960, 1, 740
5. J. Tirouflet and J. P. Chanè, Compt. rend., 1965, 245, 80
6. P. Fournari, Dissertation, Dijon, 1961.
7. S. Clementi and G. Marino, Chem. Comm., 1970, 1642.
8. P. Linda, G. Marino, and S. Pignataro, Ricerca sci., 1969, 39, 666.
9. J. H. D. Eland, Internat. J. Mass. Spectrometry Ion Phys., 1969, 2, 471.
10. K. Watanabe, T. Nakayama, and J. Mottl, J. Quant. Spectroscopy Radiative Transfer, 1962, 2, 369.
11. C. J. Varsel, F. A. Morrell, F. E. Resnik, and W. A. Powell, Analyt. Chem., 1960, 32, 182.
12. V. I. Khvostenko, Zhur. fiz. Khim., 1962, 36, 389.
13. H. C. Brown and Y. Okamoto, J. Amer. Chem. Soc., 1958, 80, 4979.
14. S. Pignataro, A. Foffani, G. Innorta, and G. Di Stefano, Z. phys. Chem. (Frankfurt), 1966, 49, 291.
15. G. F. Krable and G. L. Kearns, J. Phys. Chem., 1962, 66. 436.
16. A. Buchs, G. P. Rossetti, and B. P. Susz, Helv. Chim. Acta, 1964, 47, 1563.
17. M. Charton, Canad. J. Chem., 1970, 48, 1748.
18. H. C. Brown and L. M. Stock, J. Amer. Chem. Soc., 1957, 79, 1421.
19. G. Marino, Atti Accad. naz. Lincei, Rend. Classe Sci. fis. mat. nat., 1965, 38, 700.
20. O. Exner and W. Simon, Coll. Czech. Chem. Comm., 1964, 29, 2016.
21. P. Linda and G. Marino, J. Chem. Soc. (B), 1968, 392.
22. P. Linda and G. Marino, Tetrahedron, 1967, 23, 1739.
23. S. Clementi, F. Genel, and G. Marino, Ricerca sci., 1967, 37, 418.
24. S. Clementi and G. Marino, Tetrahedron, 1969, 25, 4599.
25. S. Clementi, P. Linda, and G. Marino, J. Chem. Soc. (B), 1970, 1153.
26. P. Linda and G. Marino, J. Chem. Soc. (B), 1970, 43.
27. P. Linda and G. Marino, Ricerca sci., 1967, 37, 424.
28. P. Reynaud and R. Delaby, Bull. Soc. chim. France, 1955, 1614.
29. H. D. Hartough, ‘Thiophen and its Derivatives,’ Interscience, New York, 1952, p. 512.
30. P. Douglas, Ber., 1892, 25, 1311.
31. R. Marquis, Compt. rend., 1901, 132, 140.
32. Yu. K. Yur’ev and N. M. Mezentseva, Zhur. obshchei Khim., 1957, 27, 179.
33. H. J. Morgan and D. P. Morrey, Tetrahedron, 1966, 22, 57.
34. R. M. Silverstein, E. E. Ryskiewicz, and C. Willard, Org. Synth., 1963, Coll. Vol. IV, p. 831.
35. R. E. Honig, J. Chem. Phys., 1948, 16, 105.
36. S. Pignataro, A. Foffani, G. Innorta, and G. Di Stefano, Adv. Mass Spectrometry, 1968, 4, 323.