Iron and copper complexes with nitrogen-containing ligands as catalysts for cyclohexane oxidation with hydrogen peroxide under mild reaction conditions

Petroleum Chemistry

Volumn 52, Issue 5, 2012, Pages 318-326

  Maksimov, A L ^a,b   Kardasheva, Yu S ^a   Predeina, V V ^a   Kluev, M V ^c   Ramazanov, D N ^b   Talanova, M Yu ^a   Karakhanov, E A ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b TOPCHIEV INSTITUTE OF PETROCHEMICAL SYNTHESIS   (Russian Federation)

^c IVANOVO STATE UNIVERSITY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

BIPYRIDYL; COPPER COMPLEXES; COPPER PHTHALOCYANINE; CYCLOHEXANE OXIDATION; CYCLOHEXANOL; CYCLOHEXANONES; HYDROPEROXIDES; IRON COMPLEX; MILD REACTION CONDITIONS; O-PHENANTHROLINE; OPTIMUM CONDITIONS; OXIDATION OF CYCLOHEXANE; TOTAL SELECTIVITY;

ACETONITRILE; COPPER COMPOUNDS; CYCLOHEXANE; HYDROGEN PEROXIDE; IRON COMPOUNDS; KETONES; OXIDATION;

LIGANDS;

EID: 84870028127     PISSN: 09655441     EISSN: 15556239     Source Type: Journal    
DOI: 10.1134/S0965544112050076     Document Type: Article

References (27)

1. M. S. Furman, Manufacture of Cyclohexanone and Adipic Acid by Oxidation of Cyclohexane (Khimiya, Moscow, 1967) [in Russian].
2. Yu. N. Kozlov, L. Gonzalez-Kuervo, G. Zyuss-Fink, and G. B. Shul'pin, Zh. Fiz. Khim. 77), 652 (2003).
3. K.-Ch. Guo, G. Khuan, and D.-K. Guo, Kinet. Katal. 47, 98 (2006).
4. Y. Yuan, H. Ji, Y. Chen, Y. Han, X. Song, Y. She, R. Zhong, Org. Proc. Res. Devel. 8, 418 (2004).
5. E. A. Karakhanov, A. L. Maksimov, and E. A. Ivanova, Izv. Akad. Nauk, Ser. Khim. 56, 598 (2007).
6. R. A. Sheldon and J. Dakka, Catal. Today 19, 215 (1994).
7. G. Goor, J. Glenneberg, and S. Jacobi, Hydrogen Peroxide, in Ullmann's Encyclopedia of Industrial Chemistry (Wiley-VCH, Weinheim, 2000).
8. B. A. Dolgoplosk and E. I. Tinyakova, Redox Systems as Source of Free Radicals (Nauka, Moscow, 1972) [in Russian].
9. V. I. Eliseeva, in Polymer Dispersions (Khimiya, Moscow, 1980) [in Russian].
10. Cellulose and Cellulose Derivatives, Ed. by N. Bikales and L. Segal (Wiley, new York, 1971).
11. V. N. Kislenko and A. A. Berlin, Usp. Khim. 50, 949 (1991).
12. G. B. Shul'pin, J. Mol. Catal., A: Chem. 189, 39 (2002).
13. E. A. Karakhanov, S. Y. Narin, and A. G. Dedov, Catal. Lett. 3, 31 (1989).
14. E. A. Karakhanov, S. Y. Narin, and A. G. Dedov, Appl. Organometall. Chem. 5, 445 (1991).
15. A. C. Melnyk, N. K. Kildahl, A. R. Rendina, and D. H. Busch, J. Am. Chem. Soc. 101, 3232 (1979).
16. K. B. Yatsimirskii and E. V. Rybak-Akimova, Teor. Eksp. Khim. 3, 309 (1986).
17. O. N. Gritsenko, E. A. Gutkina, Kh. Ammon, et al., Zh. Neorg. Khim. 52, 97 (2007).
18. A. C. Silva, T. L. Fernandez, N. M. F. Carvalho, et al., Appl. Catal. A: Gen. 317, 154 (2007).
19. N. M. F. Carvalho, A. Horn, and O. A. C. Antunes, Appl. Catal. A: Gen. 305, 140 (2006).
20. E. A. Karakhanov, S. Yu. Narin, T. Yu. Filippova, E. A. Ivanova, S. M. Volkov, A. G. Dedov, Neftekhimiya 27, 791 (1987).
21. F. P. Canhota, G. C. Salomao, N. M. F. Carvalho, and O. A. C. Antunes, Catal. Commun. 9), 182 (2008).
22. C. Detoni, N. M. F. Carvalho, D. A. G. Aranda, et al., Appl. Catal. A: Gen. 365, 281 (2009).
23. P. Roy and M. Manassero, Dalton Trans. 39, 1539 (2010).
24. A. A. Shteinman, Izv. Akad. Nauk, Ser. Khim., No. 10, 1712 (2001).
25. Yu. N. Kozlov, G. V. Nizova, and G. B. Shul'pin, Zh. Fiz. Khim. 78, 248 (2004).
26. A. O. Terent'ev, M. M. Platonov, A. S. Kashin, and G. I. Nikishin, Tetrahedron 64, 7944 (2008).
27. J. Bergendahl, S. Hubbard, and D. Grasso, J. Hazard. Mater. 99, 43 (2003).