Acid-base catalyses by dimeric disilicoicosatungstates and divacant γ-Keggin-type silicodecatungstate parent: Reactivity of the polyoxometalate compounds controlled by step-by-step protonation of lacunary W{double bond, long}O sites

Journal of Organometallic Chemistry

Volumn 692, Issue 1-3, 2007, Pages 455-459

  Yoshida, Akihiro ^a   Hikichi, Shiro ^a,b   Mizuno, Noritaka ^a,b  

^a UNIVERSITY OF TOKYO   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Acid and base catalyst; C C bond formation; Polyoxometalate

Indexed keywords

CATALYSIS; CATALYST ACTIVITY; DIMERS; MOLECULAR STRUCTURE; ORGANOMETALLICS; PROTONS;

ACID AND BASE CATALYST; C-C BOND FORMATION; KNOEVENAGEL CONDENSATION; POLYOXOMETALATE;

TUNGSTEN COMPOUNDS;

EID: 33845668016     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2006.05.061     Document Type: Article

References (49)

1. Pope M.T. Heteropoly and Isopoly Oxometalates (1983), Springer-Verlag, Berlin
2. Pope M.T., and Müller A. Angew. Chem., Int. Ed. Engl. 30 (1991) 34
3. In: Hill C.L. (Ed). Thematic issue on "Polyoxometalates". Chem. Rev. 98 (1998) 1
4. In: Pope M.T., and Müller A. (Eds). Polyoxometalate Chemistry: From Topology via Self-Assembly to Applications (2001), Kluwer, Dordrecht
5. In: Yamase T., and Pope M.T. (Eds). Polyoxometalate Chemistry for Nano-Composite Design (2002), Kluwer, Dordrecht
6. Pope M.T. In: Wedd A.G. (Ed). Comprehensive Coordination Chemistry II: Transition Metal Groups 3-6 vol. 4 (2004), Elsevier Science, New York 635 (Chapter 4.10)
7. Hill C.L., Chrisina C., and McCartha M.P. Coord. Chem. Rev. 143 (1995) 407
8. Okuhara T., Mizuno N., and Misono M. Adv. Catal. 41 (1996) 113
9. Neumann R. Prog. Inorg. Chem. 47 (1998) 317
10. Kozhevnikov I.V. Catalysis by Polyoxometalates (2002), John Wiley & Sons, Ltd., Chichester, England
11. Hill C.L. In: Wedd A.G. (Ed). Comprehensive Coordination Chemistry II: Transition Metal Groups 3-6 vol. 4 (2004), Elsevier Science, New York 679 (Chapter 4.11)
12. Mizuno N., Kamata K., and Yamaguchi K. Surface and Nanomolecular Catalysis (2006), Taylor and Francis group, LLC, New York p. 463
13. Kozhevnikov I.V. Chem. Rev. 98 (1998) 171
14. Mizuno N., and Misono M. Chem. Rev. 98 (1998) 199
15. Misono M. Chem. Commun. (2001) 1141
16. Meuzelaar G.J., Maat L., Sheldon R.A., and Kozhevnikov I.V. Catal. Lett. 45 (1997) 249
17. Kaur J., Griffin K., Harrison B., and Kozhevnikov I.V. J. Catal. 208 (2002) 448
18. Kozhevnikova E.F., Derouane E.G., and Kozhevnikov I.V. Chem. Commun. (2002) 1178
19. da Silva K.A., Robles-Dutenhefner P.A., Sousa E.M.B., Kozhevnikova E.F., Kozhevnikov I.V., and Gusevskaya E.V. Catal. Commun. 5 (2004) 425
20. Firouzabadi H., Iranpoor N., and Jafari A.A. J. Organomet. Chem. 690 (2005) 1556
21. Canny J., Tézé A., Thouvenot R., and Hervé G. Inorg. Chem. 25 (1986) 2114
22. Tézé A., and Hervé G. Inorg. Synth. 27 (1990) 85
23. Canny J., Thouvenot R., Tézé A., Hervé G., Leparulo-Loftus M., and Pope M.T. Inorg. Chem. 30 (1991) 976
24. Wassermann K., Lunk H.-J., Palm R., Fuchs J., Steinfeldt N., Stösser R., and Pope M.T. Inorg. Chem. 35 (1996) 3273
25. Zhang X.-Y., O'Connor C.J., Jameson G.B., and Pope M.T. Inorg. Chem. 35 (1996) 30
26. Nozaki C., Kiyoto I., Minai Y., Misono M., and Mizuno N. Inorg. Chem. 38 (1999) 5724
27. Kamata K., Yonehara K., Sumida Y., Yamaguchi K., Hikichi S., and Mizuno N. Science 300 (2003) 964
28. Kamata K., Nakagawa Y., Yamaguchi K., and Mizuno N. J. Catal. 224 (2004) 224
29. Mizuno N., Yamaguchi K., and Kamata K. Coord. Chem. Rev. 249 (2005) 1944
30. The computational study on the structural nature of 1 has been reported recently:. Musaev D.G., Morokuma K., Geletii Y.V., and Hill C.L. Inorg. Chem. 43 (2004) 7702
31. Yoshida A., Yoshimura M., Uehara K., Hikichi S., and Mizuno N. Angew. Chem., Int. Ed. 45 (2006) 1956
32. Mukaiyama T., Banno K., and Narasaka K. J. Am. Chem. Soc. 96 (1974) 7503
33. Kobayashi S., and Manabe K. Acc. Chem. Res. 35 (2002) 209
34. Mukaiyama T. Angew. Chem., Int. Ed. 43 (2004) 5590
35. Ooi T., Takahashi M., and Maruoka K. J. Am. Chem. Soc. 118 (1996) 11307
36. Sasidharan M., Raju S.V.N., Srinivasan K.V., Paul V., and Kumar R. Chem. Commun. (1996) 129
37. Raju S.V.N., Ponrathnam S., Rajan C.R., and Srinivasan K.V. Synlett (1996) 239
38. Sodeoka M., Tokunoh R., Miyazaki F., Hagiwara E., and Shibasaki M. Synlett (1997) 463
39. Chen C., Hon S., and Weng S. Synlett (1999) 816
40. Nakamura H., Matsuhasi H., and Arata K. Synlett (2000) 668
41. Ohkouchi M., Masui D., Yamaguchi M., and Yamagishi T. J. Mol. Catal. A 170 (2001) 1
42. Snider B.B. Acc. Chem. Res. 13 (1980) 426
43. Snider B.B. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis vol. 2 (1991), Pergamon, Oxford 527
44. Nakatani Y., and Kawashima K. Synthesis (1978) 147
45. Aggarwal V.K., Vennall G.P., Davey P.N., and Newman C. Tetrahedron Lett. 39 (1998) 1997
46. 2-soluble substrate adduct.
47. March J. Advanced Organic Chemistry. third ed. (1985), John Wiley & Sons, Tronto p. 835
48. Nakagawa Y., Kamata K., Kotani M., Yamaguchi K., and Mizuno N. Angew. Chem., Int. Ed. 44 (2005) 5136
49. Goto Y., Kamata K., Yamaguchi K., Uehara K., Hikichi S., and Mizuno N. Inorg. Chem. 45 (2006) 2347