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Abstrakty
Three resin-based m-oxo diiron(III) interface catalysts have been successfully prepared to model the functional properties of methane monooxygenase (MMO). The catalysts were characterized and exhibited the catalytic activities in the oxidation of alkanes to responding alcohols and ketones in acetonitrile at room temperature by 30% hydroperoxide (H2O2) or tert-butyl hydroperoxide (TBHP) as the oxidants. For 2,6-di-tert-butylphenol as the substrate, the C-C coupling was found in the two reaction systems. The reaction mechanisms were proposed with the predominant radical mechanism.
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Tom
Strony
163--168
Opis fizyczny
Bibliogr. 26 poz., rys.
Twórcy
autor
autor
autor
autor
- Department of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China phone and Fax: 0086-20-87110234, lzhangce@scut.edu.cn
Bibliografia
- 1. Costas M., Chen K. and Que J.L., Coord. Chem. Rev., 200-202, 517 (2000).
- 2. Fontecave M., Menage S. and Duboc-Toia C., Coord Chem. Rev., 178-180, 1555 (1998).
- 3. Solomon E.I., Brunold T.C., Davis M.I., Kemsley J.N., Lee S.-K., Lehnert N., Neese R, Skulan A.J.,Yang Y.-S. and Zhou J., Chem. Rev, 100, 235 (2000).
- 4. He C. and Mishina Y., Curr. Opin. Chem. Biol., 8, 201 (2004).
- 5. Tsien H.C., Brusseau G.A. and Hanson R.S., Appl. Environ. Microbiol., 55, 3155 (1989).
- 6. Doboc-Toia C., Menage S., Lambeaux C. and Fontecave M., Tetrahedron Lett., 38, 3727 (1997).
- 7. Menage S., Vincent J.M., Lambeaux C., Chottard G., Grand A. and Fontecave M., Inorg. Chem., 32,4766 (1993).
- 8. He C. and Lippard S.J., Tetrahedron, 56, 8245 (2000).
- 9. He C. and Lippard S.J., Inorg. Chem., 40, 1414 (2001).
- 10. Barrios A.M. and Lippard S.J., J. Am. Chem. Soc., 121, 11751 (1999).
- 11. Kuzelka J., Spingler B. and Lippard S.J., Inorg. Chim. Acta, 337, 212 (2002).
- 12. Sergey V.K. and Elena V.R.A., Inorg. Chem., 40, 2220 (2001).
- 13. Leising R.A., Kim J., Perez M.A. and Que J.L., J. Am. Chem. Soc., 115, 9524 (1993).
- 14. Mezó G., Mihala M., Koczan G. and Hudecz F., Tetrahedron, 54, 6757 (1998).
- 15. Pei Y., Houghten R.A. and Kiely J.S., Tetrahedron Lett., 38, 3349 (1997).
- 16. Krehnak V., Smith J. and Vagner J., Tetrahedron Lett., 42, 1627 (2001).
- 17. Berteina S., and Mesmaeker A. D., Tetrahedron Lett., 39, 5759 (1998).
- 18. Luo Y.L., Zhang L., Zong M.H., Menage S. and Fontecave M., Polish J. Chem., 80, 1407 (2006).
- 19. Menage S., Vincent J.M., Lambeaux G. and Fontecave M., J. Mol. Catal. A: Chem., 113, 61 (1996).
- 20. Türk H. and Cimen Y., J. Mol. Catal A: Chem., 234, 19 (2005).
- 21. Cimen Y. and Ttirk H., J. Mol. Catal A: Chem., 265, 237 (2007).
- 22. Grootboom N. and Nyokong T., J. Mol. Catal. A: Chem., 179, 113 (2002).
- 23. Kharasch M.S. and Joshi B.S., J. Org. Chem., 22, 1439 (1957).
- 24. Bedell S.A. and Martell A.E., Inorg. Chem., 22, 364 (1983).
- 25. Kohara L, Fujiyama H., Iwai K., Nishiyama S. and Tsuruya S., J. Mol. Catal. A: Chem., 153,93 (2000).
- 26. Comuzzi C., Melchior A., Polese R, Portanova R. and Tolazzi M., Inorg. Chim. Acta, 355, 57 (2003).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ6-0025-0052