Redox properties and oxidation catalysis of group 5 metal (V, Nb, Ta)-containing Keggin and Wells-Dawson heteropolyacid (HPA) catalysts

Applied Catalysis A: General

Volumn 373, Issue 1-2, 2010, Pages 201-207

  Park, Dong Ryul ^a   Park, Sunyoung ^a   Bang, Yongju ^a   Song, In Kyu ^a  

^a Seoul National University   (South Korea)

Author keywords

Benzyl alcohol oxidation; Group 5 metal substitution; Heteropolyacid catalyst; Reduction potential; UV visible absorption edge energy

Indexed keywords

ABSORPTION EDGES; BENZYL ALCOHOL OXIDATION; ELECTROCHEMICAL METHODS; HETEROPOLY ACIDS; HETEROPOLYACID CATALYST; METAL SUBSTITUTION; MODEL REACTIONS; OXIDATION CATALYSIS; REDOX PROPERTY; REDUCTION POTENTIAL; UV VISIBLE SPECTROSCOPY; UV-VISIBLE ABSORPTION; VAPOR PHASE; WELLS-DAWSON;

ABSORPTION; ALDEHYDES; CATALYSIS; CATALYSTS; INFRARED SPECTROPHOTOMETERS; METALS; OXIDATION; REDUCTION; TANTALUM; ULTRAVIOLET SPECTROSCOPY; WELLS;

ABSORPTION SPECTROSCOPY;

EID: 74249101295     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2009.11.018     Document Type: Article

References (48)

1. Pope M.T., and Müller A. Polyoxometalates: From Platonic Solids to Anti-retroviral Activity (1994), Kluwer Academic Publishers, Dordrecht, The Netherlands
2. Hill C.L., and Prosser-McCartha C.M. Coord. Chem. Rev. 143 (1995) 407-455
3. Kozhevnikov I.V. Chem. Rev. 98 (1998) 171-198
4. Okuhara T., Mizuno N., and Misono M. Adv. Catal. 41 (1996) 113-252
5. Mizuno N., and Misono M. Chem. Rev. 98 (1998) 199-217
6. Song I.K., and Barteau M.A. Korean J. Chem. Eng. 19 (2002) 567-573
7. Keggin J.F. Nature 131 (1933) 908-909
8. Kozhevnikov I.V. Catal. Rev. - Sci. Eng. 37 (1995) 311-352
9. Lim S.S., Kim Y.H., Park G.I., Lee W.Y., Song I.K., and Youn H.K. Catal. Lett. 60 (1999) 199-204
10. Mori H., Mizuno N., and Misono M. J. Catal. 131 (1990) 133-142
11. Dawson B. Acta Cryst. 6 (1953) 113-126
12. Mizuno N., Weiner H., and Finke R.G. J. Mol. Catal. A 114 (1996) 15-28
13. Briand L.E., Baronetti G.T., and Thomas H.J. Appl. Catal. A: Gen. 256 (2003) 37-50
14. Matkovic S.R., Valle G.M., Gambaro L.A., and Briand L.E. Catal. Today 133-135 (2008) 192-199
15. Weber R.S. J. Phys. Chem. 98 (1994) 2999-3005
16. Eguchi K., Seiyama T., Yamazoe N., Katsuki S., and Taketa H. J. Catal. 111 (1988) 336-344
17. Kaba M.S., Song I.K., and Barteau M.A. J. Phys. Chem. 100 (1996) 19577-19581
18. Youn M.H., Park D.R., Jung J.C., Kim H., Barteau M.A., and Song I.K. Korean J. Chem. Eng. 24 (2007) 51-54
19. Song I.K., and Barteau M.A. J. Mol. Catal. A 182-183 (2002) 185-193
20. Song I.K., Kaba M.S., Nomiya K., Finke R.G., and Barteau M.A. J. Mol. Catal. A 262 (2007) 216-226
21. Altenau J.J., Pope M.T., Prados R.A., and So H. Inorg. Chem. 14 (1975) 417-421
22. Keita B., and Nadjo L. Mater. Chem. Phys. 22 (1989) 77-103
23. Pope M.T., and Varga Jr. G.M. Inorg. Chem. 5 (1966) 1249-1254
24. Kozhevnikov I.V. Catalysts for Fine Chemical Synthesis (2002), Wiley, West Sussex, England
25. Grigoriev V.A., Hill C.L., and Weinstock I.A. J. Am. Chem. Soc. 122 (2000) 3544-3545
26. Sadakane M., and Steckhan E. Chem. Rev. 98 (1998) 219-238
27. Barteau K.P., Lyons J.E., Song I.K., and Barteau M.A. Top. Catal. 41 (2006) 55-62
28. Yamase T. Chem. Rev. 98 (1998) 307-326
29. Youn M.H., Kim H., Jung J.C., Song I.K., Barteau K.P., and Barteau M.A. J. Mol. Catal. A 241 (2005) 227-232
30. Ali B.E., El-Ghanam A.M., and Fettouhi M. J. Mol. Catal. A 165 (2001) 283-290
31. Lee J.K., Melsheimer J., Berndt S., Mestl G., Schlögl R., and Köhler K. Appl. Catal. A: Gen. 214 (2001) 125-148
32. Shinachi S., Matsushita M., Yamaguchi K., and Mizuno N. J. Catal. 233 (2005) 81-89
33. Okumura K., Yamashita K., Yamada K., and Niwa M. J. Catal. 245 (2007) 75-83
34. Wachs I.E., Briand L.E., Jehng J.-M., Burcham L., and Gao X. Catal. Today 57 (2000) 323-330
35. Ushikubo T. Catal. Today 57 (2000) 331-338
36. Tanabe K. Catal. Today 78 (2003) 65-77
37. Akimoto M., Tsuchida Y., Sato K., and Echigoya E. J. Catal. 72 (1981) 83-94
38. Konishi Y., Sakata K., Misono M., and Yoneda Y. J. Catal. 77 (1982) 169-179
39. Serwicka E.M., Broclawik E., Brückman K., and Haber J. Catal. Lett. 2 (1989) 351-360
40. Centi G., Nieto J.L., Iapalucci C., Brückman K., and Serwicka E.M. Appl. Catal. 46 (1989) 197-212
41. Mbomekalle I.-M., Lu Y.W., Keita B., and Nadjo L. Inorg. Chem. Commun. 7 (2004) 86-90
42. Park D.R., Song S.H., Hong U.G., Seo J.G., Jung J.C., and Song I.K. Catal. Lett. 132 (2009) 363-369
43. Kubelka P., and Munk F. Z. Tech. Phys. 12 (1931) 593-601
44. Pope M.T. Heteropoly and Isopoly Oxometalates (1983), Springer-Verlag, New York
45. O'Donnell S.E., and Pope M.T. J. Chem. Soc., Dalton Trans. (1976) 2290-2297
46. Massart R., Contant R., Fruchart J.M., Ciabrini J.P., and Fournier M. Inorg. Chem. 16 (1977) 2916-2921
47. Yadav G.D., and Mistry C.K. J. Mol. Catal. A 172 (2001) 135-149
48. Lingaiah N., Reddy K.M., Babu N.S., Rao K.N., Suryanarayana I., and Prasad P.S.S. Catal. Commun. 7 (2006) 245-250