Aqueous hydrogenation of carbon dioxide catalysed by water-soluble ruthenium aqua complexes under acidic conditions

Chemical Communications

Volumn , Issue 23, 2004, Pages 2714-2715

  Hayashi, Hideki ^a   Ogo, Seiji ^a   Fukuzumi, Shunichi ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON DIOXIDE; RUTHENIUM; WATER;

ACIDITY; AQUEOUS SOLUTION; ARTICLE; CATALYSIS; HYDROGENATION; REDUCTION; SOLUBILITY; X RAY ANALYSIS;

EID: 11144292323     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b411633j     Document Type: Article

References (24)

1. (a) F. Joó, in Catalysis by Metal Complexes, Vol. 23, Aqueous Organometallic Catalysis, Kluwer Academic Publishers, Dordrecht, The Netherlands, 2001, pp. 113-122;
2. (b) W. Leitner, E. Dinjus and F. Gaßner, in Aqueous-Phase Organometallic Catalysis, Concepts and Applications, ed. B. Cornils and W. A. Hermann, Wiley-VCH, Weinheim, Germany, 1998, pp. 486-498;
3. (c) A. Behr, Carbon Dioxide Activation by Metal Complexes, VCH, Weinheim, Germany, 1988;
4. (d) P. G. Jessop, T. Ikariya and R. Noyori, Chem. Rev., 1995, 95, 259;
5. (e) W. Leitner, Angew. Chem., Int. Ed. Engl., 1995, 34, 2207.
6. (a) Handbook of Chemistry and Physics, 83rd edn., ed. D. R. Lide, CRC Press, Boca Raton, FL, 2002;
7. (b) F. A. Cotton, G. Wilkinson, C. A. Murillo and M. Bochmann, in Advanced Inorganic Chemistry, 6th edn., Wiley-Interscience, New York, 1999, pp. 226-227.
8. (a) M. M. Taqui Khan, S. B. Halligudi and S. Shukla, J. Mol. Catal., 1989, 57, 47;
9. (b) F. Gassner and W. Leitner, J. Chem. Soc., Chem. Commun., 1993, 1465;
10. (c) F. Joó, G. Laurenczy, L. Nádasdi and J. Elek, Chem. Commun., 1999, 971;
11. (d) G. Laurenczy, F. Joó and L. Nádasdi, Inorg. Chem., 2000, 39, 5083;
12. (e) F. Joó, G. Laurenczy, P. Karády, J. Elek, L. Nádasdi and R. Roulet, Appl. Organomet. Chem., 2000, 14, 857;
13. (f) J. Elek, L. Nádasdi, G. Papp, G. Laurenczy and F. Joó, Appl. Catal., A, 2003, 255, 59;
14. (g) A. Kathó, Z. Opre, G. Laurenczy and F. Joó, J. Mol. Catal. A: Chem, 2003, 204-205, 143;
15. (h) Y. Himeda, N. Onozawa-Komatsuzaki, H. Sugihara, H. Arakawa and K. Kasuga, Organometallics, 2004, 23, 1480;
16. (i) H. Horváth, G. Laurenczy and A. Kathó, J. Organomet. Chem., 2004, 689, 1036.
17. 2 without base have been reported, although the pH values of the solutions were not described.
18. (a) H. Hayashi, S. Ogo, T. Abura and S. Fukuzumi, J. Am. Chem. Soc., 2003, 125, 14266;
19. (b) S. Ogo, K. Uehara, T. Abura, Y. Watanabe and S. Fukuzumi, Organometallics, 2004, 23, 3047;
20. (c) S. Ogo, T. Abura and Y. Watanabe, Organometallics, 2002, 21, 2964.
21. 2O, probably because of the instability under the acidic conditions.
22. S. Ogo, H. Nakai and Y. Watanabe, J. Am. Chem. Soc., 2002, 124, 597.
23. (a) P. J. Brothers, Prog. Inorg. Chem., 1981, 28, 1;
24. (b) B. R. James and M. T. Ashby, in Inorganic Reactions and Methods, Vol. 16, Reactions Catalyzed by Inorganic Compounds, ed. A. D. Norman, VCH Publishers, New York, USA, 1991, pp. 71-77.