Synthesis and structural characterization of a monomeric di-copper-substituted silicotungstate [γ-H2SiW10O36Cu2(μ-1,1-N3)2]4- and the catalysis of oxidative homocoupling of alkynes

Journal of Catalysis

Volumn 258, Issue 1, 2008, Pages 121-130

  Yamaguchi, Kazuya ^a,b   Kamata, Keigo ^a,b   Yamaguchi, Syuhei ^b   Kotani, Miyuki ^b   Mizuno, Noritaka ^a,b  

^a UNIVERSITY OF TOKYO   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Alkyne; Copper; Diyne; Homocoupling; Polyoxometalate

Indexed keywords

(O-SEC.-BUTYLDITHIOCARBONATIO-S ,S') COPPER; STRUCTURAL CHARACTERIZATIONS; SYNTHESIS (OF CHIRAL IONIC LIQUIDS);

COPPER;

EID: 47749135211     PISSN: 00219517     EISSN: 10902694     Source Type: Journal    
DOI: 10.1016/j.jcat.2008.06.004     Document Type: Article

References (49)

1. Pope M.T. Heteropoly and Isopoly Oxometalates (1983), Springer-Verlag, Berlin pp. 1-165
2. Hill C.L., Chrisina C., and Prosser-McCartha M. Coord. Chem. Rev. 143 (1995) 407
3. Okuhara T., Mizuno N., and Misono M. Adv. Catal. 41 (1996) 113
4. Mizuno N., and Misono M. Chem. Rev. 98 (1998) 199
5. Neumann R. Prog. Inorg. Chem. 47 (1998) 317
6. Kozhevnikov I.V. Chem. Rev. 98 (1998) 171
7. Mizuno N., Yamaguchi K., and Kamata K. Coord. Chem. Rev. 249 (2005) 1944
8. Mizuno N., Kamata K., and Yamaguchi K. In: Richards R. (Ed). Surface and Nanomolecular Catalysis (2006), Taylor and Francis Group, New York 463-492
9. Tézé A., and Hervé G. Inorg. Synth. 27 (1990) 85
10. Ribas J., Escuer A., Monfort M., Vicente R., Cortés R., Lezama L., and Rojo T. Coord. Chem. Rev. 193-195 (1999) 1027
11. Cenini S., Gallo E., Caselli A., Ragaini F., Fantauzzi S., and Piangiolino C. Coord. Chem. Rev. 250 (2006) 1234
12. Mialane P., Dolbecq A., Marrot J., and Sécheresse F. Angew. Chem. Int. Ed. 43 (2004) 2274
13. Mialane P., Dolbecq A., Marrot J., Rivière E., and Sécheresse F. Chem. Eur. J. 11 (2005) 1771
14. Mialane P., Duboc C., Marrot J., Rivière E., Dolbecq A., and Sécheresse F. Chem. Eur. J. 12 (2006) 1950
15. Mialane P., Dolbecq A., and Sécheresse F. Chem. Commun. (2006) 3477
16. Siemsen P., Livingston R.C., and Diederich F. Angew. Chem. Int. Ed. 39 (2000) 2632
17. Hansen L., and Boll P.M. Phytochemistry 25 (1986) 285
18. Matsunaga H., Katano M., Yamamoto H., Fujito H., Mori M., and Takata K. Chem. Pharm. Bull. 38 (1990) 3480
19. Glaser C. Ber. Dtsch. Chem. Ges. 2 (1869) 422
20. Hay A.S. J. Org. Chem. 27 (1962) 3320
21. Campbell I.D., and Eglinton G. Org. Synth. 45 (1965) 39
22. Auer S.M., Schneider M., and Baiker A. J. Chem. Soc. Chem. Commun. (1995) 2057
23. Li J., and Jiang H. Chem. Commun. (1999) 2369
24. Salazar R., Fomina L., and Fomine S. Polym. Bull. 47 (2001) 151
25. Sharifi A., Mirzaei M., and Naimi-Jamal M.R. J. Chem. Res. (2002) 628
26. Yadav J.S., Reddy B.V.S., Reddy K.B., Gayathri K.U., and Prasad A.R. Tetrahedron Lett. 44 (2003) 6493
27. Wanga L., Yana J., Lia P., Wanga M., and Su C. J. Chem. Res. (2005) 112
28. Lu X., Zhang Y., Luo C., and Wang Y. Synth. Commun. 36 (2006) 2503
29. Rossi R., Carpita A., and Bigelli C. Tetrahedron Lett. 26 (1985) 523
30. Liu Q., and Burton D.J. Tetrahedron Lett. 38 (1997) 4371
31. Herrmann W.A., Böhm V.P.W., Gstöttmayr C.V.K., Grosche M., Reisinger C.-P., and Weskamp T. J. Organomet. Chem. 618 (2001) 616
32. Lei A., Srivastava M., and Zhang X. J. Org. Chem. 67 (2002) 1969
33. Fairlamb I.J.S., Bäuerlein P.S., Marrison L.R., and Dickinson J.M. Chem. Commun. (2003) 632
34. Li J., Liang Y., and Zhang X.-D. Tetrahedron 61 (2005) 1903
35. Li J.-H., Liang Y., and Xie Y.-X. J. Org. Chem. 70 (2005) 4393
36. Kamata K., Yamaguchi S., Kotani M., Yamaguchi K., and Mizuno N. Angew. Chem. Int. Ed. 47 (2008) 2407
37. In: Perrin D.D., and Armarego W.L.F. (Eds). Purification of Laboratory Chemicals. third ed. (1988), Pergamon Press, Oxford 80-388
38. Casella L., Carugo O., Gullotti M., Garofani S., and Zanello P. Inorg. Chem. 32 (1993) 2056
39. Brown I.D., and Altermatt D. Acta Crystallogr. Sect. B: Struct. Sci. 41 (1985) 244
40. Brese N.E., and O'Keeffe M. Acta Crystallogr. Sect. B: Struct. Sci. 47 (1991) 192
41. Lyon D.K., Miller W.K., Novet T., Domaille P.J., Evitt E., Johnson D.C., and Finke R.G. J. Am. Chem. Soc. 113 (1991) 7209
42. Long D.-L., Streb C., Song Y.-F., Mitchell S., and Cronin L. J. Am. Chem. Soc. 130 (2008) 1830
43. Bohlmann F., Schönowsky H., Inhoffen E., and Grau G. Chem. Ber. 97 (1964) 794
44. Pate J.E., Ross P.K., Thamann T.J., Reed C.A., Karlin K.D., Sorrell T.N., and Solomon E.I. J. Am. Chem. Soc. 111 (1989) 5198
45. Sen S., Mitra S., Hughes D.L., Rosair G., and Desplenches C. Polyhedron 26 (2007) 1740
46. Allevi M., Bonizzoni M., and Fabbrizzi L. Chem. Eur. J. 13 (2007) 3787
47. Yam V.W., Lo K.K., Fung W.K., and Wang C. Coord. Chem. Rev. 17 (1998) 17
48. Hathaway B.J., and Billing D.E. Coord. Chem. Rev. 5 (1970) 143
49. Connors K.A. Chemical Kinetics, The Study of Reaction Rates in Solution (1990), VCH Publishers, New York pp. 292-305