Catalysis of the reaction of methallyl chloride with CCl4 by some iron compounds or the system: Fe(CO)5-solvent
Organic and Biological Chemistry
Received:
- 20 Downloads
Conclusions
- 1.
A study was made of the catalytic effect of Fe(CO)5, Fe2(CO)9, Fe(acetylacetonate)3, FeCl3,π-C3H5Fe(CO)3I, and the system Fe(CO)5-solvent on the rate and direction of the radical reaction of methallyl chloride with CCl4 at 95°.
- 2.
All of the catalysts, especially FeCl3, proved to be effective in ligand transfer and suppressed the development of the kinetic chain involving the free chlorine atom. The maximum rate of the process was observed with Fe(CO)5. Tetrahydrofuran, isopropanol and dimethylformamide possessed a high cocatalytic activity.
Keywords
Iron Chloride Catalysis Chlorine Isopropanol
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Preview
Unable to display preview. Download preview PDF.
Literature cited
- 1.R. Kh. Freidlina, N. A. Grigor'ev, T. A. Onishchenko, and B. A. Englin. Dokl. Akad. Nauk SSSR,205, 602 (1972).Google Scholar
- 2.B. A. Englin and B. N. Osipov, Izv. Akad. Nauk SSSR, Ser. Khim.,1971, 65.Google Scholar
- 3.R. Kh. Freidlina, R. D. Ismailov, and B. A. Englin, Izv. Akad. Nauk SSSR, Ser. Khim.,1972, 2320.Google Scholar
- 4.B. A. Englin, R. D. Ismailov, and R. Kh. Freidlina, Izv. Akad. Nauk SSSR, Ser. Khim.,1972, 1331.Google Scholar
- 5.B. A. Englin, R. D. Ismailov, and R. Kh. Freidlina, Izv. Akad. Nauk SSSR, Ser. Khim.,1972, 1517.Google Scholar
- 6.A. Weissberger, E. S. Proskauer, J. A. Riddick, and E. E. Toops, Jr., Organic Solvents [Russian translation], IL (1958).Google Scholar
- 7.E. Speyer and H. Wolf, Chem. Ber.,60, 1424 (1927).Google Scholar
- 8.R. G. Charles and M. A. Powlikowski, J. Phys. Chem.,62, 440 (1958).Google Scholar
- 9.A. N. Nesmeyanov and J. J. Kritskaya, J. Organometal. Chem.,14, 387 (1968).Google Scholar
- 10.V. Gutman, Coordination Chem. Rev.,2, 239 (1967).Google Scholar
- 11.B. A. Englin, V. A. Volovoi, L. G. Zelenskaya, T. A. Babushkina, G. K. Semin, V. B. Bondarev, B. N. Osipov, and R. Kh. Freidlina, Izv. Akad. Nauk SSSR, Ser. Khim.,1970, 2700.Google Scholar
- 12.B. A. Englin, B. N. Osipov, V. A. Valovoi, T. A. Babushkina, G. K. Semin, V. B. Bondarev, and R. Kh. Freidlina, Izv. Akad. Nauk SSSR, Ser. Khim.,1968, 1251.Google Scholar
- 13.J. J. Shipman, V. L. Folt, and S. Krimm, Spectrochim. Acta,18, 603 (1962).Google Scholar
- 14.L. J. Bellamy, Infrared Spectra of Complex Molecules [Russian translation], IL (1963), p. 470.Google Scholar
- 15.G. K. Semin, Dokl. Akad. Nauk SSSR,158, 1169 (1964).Google Scholar
- 16.J. K. Kochi and P. E. Mocadlo, J. Org. Chem.,30, 1134 (1965).Google Scholar
- 17.M. Asscher and D. Vofsi, J. Chem. Soc., B,1968, 947.Google Scholar
- 18.H. Werner, Angew. Chem., Internal. Edit.,7, 930 (1968); R. J. Angelici, Organometal. Chem. Rev.,3, 173 (1968).Google Scholar
Copyright information
© Consultants Bureau 1973