Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Epoxidation of Olefins by Cobalt-Containing Polyoxotungstate and Potassium Monopersulfate in Aqueous Solution

  • Published : 2002.07.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Metal-Catalyzed Oxidations of Organic Compounds; Sheldon, R. A.; Kochi, J. K., Eds.; Academic Press: New York, 1981.
  2. Catalytic Oxidations with Hydrogen Peroxide as Oxidant; Strukul, G., Ed.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1992.
  3. Catalytic Activation of Dioxygen by Metal Complexes; Simandi, L. I., Ed.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1992.
  4. McLain, J. L.; Lee, J.; Groves, J. T. In Biomimetic Oxidations Catalyzed by Transition Metal Complexes; Meunier, B., Ed.; Imperial College Press: London, 2000; pp 91-169.
  5. Watanabe, Y. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic: New York, 2000; Vol. 4, Chapter 30, pp 97-117.
  6. Harris, D. L. Curr. Opin. Chem. Biol. 2001, 5, 724- 735. https://doi.org/10.1016/S1367-5931(01)00272-1
  7. Schroder, D.; Shaik, S.; Schwarz, H. Acc. Chem. Res. 2000, 33, 139-145. https://doi.org/10.1021/ar990028j
  8. Newcomb, M.; Toy, P. H. Acc. Chem. Res. 2000, 33, 449-455. https://doi.org/10.1021/ar960058b
  9. Sono, M.; Roach, M. P.; Coulter, E. D.; Dawson, J. H. Chem. Rev. 1996, 96, 2841-2887. https://doi.org/10.1021/cr9500500
  10. Metalloporphyrins in Catalytic Oxidations; Sheldon, R. A., Ed.; Marcel Dekker, Inc.: New-York, 1994.
  11. Metalloporphyrins Catalyzed Oxidations; Montanari, F., Casella, L., Eds., Kluwer Academic Publishers: Dordrecht, The Netherlands, 1993.
  12. Hill, C. L., Ed. Polyoxometalates. Chem. Rev. 1998, 98, 1-390. https://doi.org/10.1021/cr960395y
  13. Boring, E.; Geletii, Y. V.; Hill, C. L. J. Am. Chem. Soc. 2001, 123, 1625-1635. https://doi.org/10.1021/ja0033133
  14. Khenkin, A. M.; Weiner, L.; Wang, Y.; Neumann, R. J. Am. Chem. Soc. 2001, 123, 8531-8542. https://doi.org/10.1021/ja004163z
  15. Nishiyama, Y.; Nakagawa, Y.; Mizuno, N. Angew. Chem. Int. Ed. 2001, 40, 3639-3641. https://doi.org/10.1002/1521-3773(20011001)40:19<3639::AID-ANIE3639>3.0.CO;2-0
  16. Weiner, H.; Hayashi, Y.; Finke, R. G. Inorg. Chem. 1999, 38, 2579-2591. https://doi.org/10.1021/ic990078k
  17. Nam, W.; Yang, S. J.; Kim, H. Bull. Korean Chem. Soc. 1996, 17,625-630. https://doi.org/10.1007/BF02699107
  18. Brevard, C.; Schimpf, R.; Tourne, G.; Tourne, C. M. J. Am. Chem.Soc. 1983, 105, 7059-7063. https://doi.org/10.1021/ja00362a008
  19. Hill, C. L.; Brown, R. B. J. Am. Chem. Soc. 1986, 108, 536- 538. https://doi.org/10.1021/ja00263a046
  20. Tourne, C. M.; Tourne, G. F.; Malik, S. A.; Weakly, J. R. J. Inorg. Nucl. Chem. 1970, 30, 3875-3890.
  21. Zonnevijile, F.; Tourne, C. M.; Tourne, G. F. Inorg. Chem. 1982, 21, 2751-2757. https://doi.org/10.1021/ic00137a042
  22. Bernadou, J.; Fabiano, A.-S.; Robert, A.; Meunier, B. J. Am.Chem. Soc. 1994, 116, 9375-9376. https://doi.org/10.1021/ja00099a083
  23. Yang, S.; Nam, W. Inorg. Chem. 1998, 37, 606-607. https://doi.org/10.1021/ic9710519
  24. Robert, A.; Meunier, B. New J. Chem. 1988, 12, 885-896.
  25. Thompson, R. C.; Wieland, P.; Appelman, E. H. Inorg. Chem. 1979, 18, 1974-1977. https://doi.org/10.1021/ic50197a051
  26. Nam, W.; Kim, I.; Lim, M. H.; Choi, H. J.; Lee, J. S.; Jang, H. G. Chem. Eur. J. 2002, 8, 2067-2071. https://doi.org/10.1002/1521-3765(20020503)8:9<2067::AID-CHEM2067>3.0.CO;2-V
  27. Nam, W.; Choi, H. J.; Han, H. J.; Cho, S. H.; Lee, H. J.; Han, S.-Y. Chem. Commun. 1999, 387-388.
  28. Yang, S. J.; Lee, H. J.; Nam, W. Bull. Korean Chem. Soc. 1998, 19, 276-278.
  29. Song, R.; Sorokin, A.; Bernadou, J.; Meunier, B. J. Org. Chem. 1997, 62, 673-678. https://doi.org/10.1021/jo961421v
  30. Labat, G.; Meunier, B. J. Org. Chem. 1989, 54, 5008-5011. https://doi.org/10.1021/jo00282a011
  31. Labat, G.; Meunier, B. New J. Chem. 1989, 13, 801-804.
  32. Daniels, J. S.; Gates, K. S. J. Am. Chem. Soc. 1996, 118, 3380- 3385. https://doi.org/10.1021/ja9510774
  33. Kawanishi, S.; Yamamoto, K.; Inoue, S. Biochem. Pharm. 1989, 38, 3491-3496. https://doi.org/10.1016/0006-2952(89)90119-6
  34. Mottley, C.; Mason, R. P. Arch. Biochem. Biophys. 1988, 267, 681-689. https://doi.org/10.1016/0003-9861(88)90077-X
  35. Gilbert, B. C.; Stell, J. K. J. Chem. Soc., Perkin Trans. 2 1990, 1281-1288.
  36. Tatsumi, T.; Yamamoto, K.; Tajima, H.; Tominaga, H. Chem. Lett. 1992, 815-818.
  37. Groves, J. T.; Nemo, T. E. J. Am. Chem. Soc. 1983, 105, 5786-5791. https://doi.org/10.1021/ja00356a015
  38. Nam, W.; Lim, M. H.; Lee, H. J.; Kim, C. J. Am. Chem. Soc. 2000, 122, 6641-6647. https://doi.org/10.1021/ja000289k
  39. Nam, W.; Jin, S. W.; Lim, M. H.; Ryu, J. Y.; Kim, C. Inorg. Chem. 2002, 41, 3647-3652. https://doi.org/10.1021/ic011145p
  40. Meunier, B.; Bernadou, J. Struct. Bonding 2000, 97, 1-35. https://doi.org/10.1007/3-540-46592-8_1
  41. Bernadou, J.; Meunier, B. Chem. Commun. 1998, 2167-2173.
  42. Lee, K. A.; Nam, W. J. Am. Chem. Soc. 1997, 119, 1916-1922. https://doi.org/10.1021/ja9629118
  43. Khenkin, A. M.; Hill, C. L. J. Am. Chem. Soc. 1993, 115, 8178-8186. https://doi.org/10.1021/ja00071a030
  44. Wadhwani, P.; Mukherjee, M.; Bandyopadhyay, D. J. Am. Chem. Soc. 2001, 123, 12430-12431. https://doi.org/10.1021/ja010730m
  45. Collman, J. P.; Chien, A. S.; Eberspacher, T. A.; Brauman, J. I. J. Am. Chem. Soc. 2000, 122, 11098-11100. https://doi.org/10.1021/ja000961d
  46. Nam, W.; Lim, M. H.; Moon, S. K.; Kim, C. J. Am. Chem. Soc. 2000, 122, 10805-10809. https://doi.org/10.1021/ja0010554
  47. Machii, K.; Watanabe, Y.; Morishima, I. J. Am. Chem. Soc. 1995, 117, 6691-6697. https://doi.org/10.1021/ja00130a007
  48. Meunier, B. Chem. Rev. 1992, 92, 1411-1456. https://doi.org/10.1021/cr00014a008
  49. Jorgensen, K. A. Chem. Rev. 1989, 89, 431-458. https://doi.org/10.1021/cr00093a001
  50. Nam, W.; Kim, I.; Kim, Y.; Kim, C. Chem. Commun. 2001, 1262-1263.

Cited by

  1. ChemInform Abstract: Epoxidation of Olefins by Cobalt-Containing Polyoxotungstate and Potassium Monopersulfate in Aqueous Solution. vol.33, pp.48, 2010, https://doi.org/10.1002/chin.200248101
  2. Epoxidation of Simple Alkenes with O2 and Isobutyraldehyde Catalyzed by Ni Catalysts Deposited on Nanoporous Carbon vol.26, pp.6, 2005, https://doi.org/10.5012/bkcs.2005.26.6.887
  3. Epoxidation of alkenes catalyzed by cobalt(II) calix[4]pyrrole vol.8, pp.3, 2002, https://doi.org/10.1016/j.catcom.2006.06.022
  4. Jacobsen catalyst as a P450 biomimetic model for the oxidation of an antiepileptic drug vol.273, pp.1, 2007, https://doi.org/10.1016/j.molcata.2007.04.003
  5. A cobalt(II) complex with anionic and neutral N-donor ligands: synthesis, crystal structure, and application as a heterogeneous catalyst for olefin epoxidation with tert-BuOOH vol.68, pp.6, 2002, https://doi.org/10.1080/00958972.2015.1007964
  6. Epoxidation of trans-stilbene with molecular oxygen over an eco-friendly heterogeneous cobalt oxide/reduced graphene oxide composite material vol.46, pp.10, 2002, https://doi.org/10.1007/s11164-020-04215-7