One-pot synthesis of alcohols from olefins catalyzed by rhodium and ruthenium complexes

Applied Catalysis A: General

Volumn 374, Issue 1-2, 2010, Pages 201-212

  Zakzeski, Joseph ^a   Lee, Hae Ryun ^a   Leung, Yi Ling ^a   Bell, Alexis T ^a  

^a University of California   (United States)

Author keywords

Alcohol; Aldehyde hydrogenation; Hydroformylation; Olefin; One pot synthesis

Indexed keywords

1-HEXENE; ALDEHYDE HYDROGENATION; CATALYST CONCENTRATION; CO CONCENTRATIONS; CO CONVERSION; GAS PARTIAL PRESSURE; GAS PRESSURES; HEPTANOL; ONE-POT SYNTHESIS; OPTIMAL CONDITIONS; OPTIMAL TEMPERATURE; REACTION MECHANISM; REACTION PARAMETERS; RESIDUAL CARBON; RU CATALYSTS; RUTHENIUM COMPLEXES; SPECTROSCOPIC EVIDENCE; STOICHIOMETRIC QUANTITIES; TRIPHENYLPHOSPHENE;

ALCOHOLS; ALDEHYDES; BOILERS; CARBON MONOXIDE; CATALYSIS; CATALYSTS; HYDROFORMYLATION; HYDROGENATION; OPTIMIZATION; PRESSURE VESSELS; PROPYLENE; RHODIUM; RHODIUM COMPOUNDS; RUTHENIUM; RUTHENIUM COMPOUNDS;

HYDROXYLATION;

EID: 74049145793     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2009.12.011     Document Type: Article

References (57)

1. Lee S.-M., Cho M.O., Park C.H., Chung Y.-C., Kim J.H., Sang B.-I., and Um Y. Energy Fuels 22 (2008) 3459
2. R.M. Jimeson, M.C. Radosevich, R.R. Stevens, US Patent 6858048 (2005).
3. R.M. Jimeson, M.C. Radosevich, R.R. Stevens, US Patent 7559961 (2009).
4. Ezeji T., Qureshi N., and Blaschek H.P. Biotech. Bioeng. 97 (2007) 1460
5. Zverlov V.V., Berezina O., Velikodvorskaya G.A., and Schwarz W.H. Appl. Microbiol. Biotechnol. 71 (2006) 587
6. Matar S., and Hatch L.F. Chemistry of Petrochemical Processes. 2nd ed. (2001), Gulf Professional, Woburn
7. In: Cornils B., and Herrmann W.A. (Eds). Applied Homogeneous Catalysis with Organometallalic Compounds. 2nd ed. (2002), Wiley-VCA, Weinheim
8. In: van Leeuwen P.W.N.M., and Claver C. (Eds). Rhodium Catalyzed Hydroformylation (2000), Kluwer Academic Publishers, Amsterdam
9. C.-Y. Hsu, J.E. Lyons, P.E. Ellis, Jr., US Patent 4524142 (1985).
10. Fache E., Santini C., Senocq F., and Basset J.M. J. Mol. Catal. 72 (1992) 337
11. Kim J.-Y., Jun M.-J., and Lee W.-Y. Polyhedron 15 (1996) 3787
12. Sanchez-Delgado R.A., Andriollo A., De Ochoa O.L., Suarez T., and Valencia N. J. Organomet. Chem. 209 (1981) 77
13. Strohmeier W., and Weigelt L. J. Organomet. Chem. 145 (1978) 189
14. Tsuji J., and Suzuki H. Chem. Lett. (1977) 1085
15. Sanchez-Delgado R.A., and De Ochoa O.L. J. Mol. Catal. 6 (1979) 303
16. Bianchini C., Lee H.M., Meli A., and Vizza F. Organometallics 19 (2000) 849
17. Xu L., Ou G., and Yuan Y. J. Organomet. Chem. 693 (2008) 3000
18. Fujitsu H., Matsumura E., Takeshita K., and Mochida I. J. Org. Chem. 46 (1981) 5353
19. Sanchez-Delgado R.A., Lee W., Choi S.R., Cho Y., and Jun M.-J. Transition Met. Chem. 16 (1991) 241
20. Kolarić S., and Šunjić V. J. Mol. Catal. A: Chem. 111 (1996) 239
21. L.H. Slaugh, R.D. Mullineaux, US Patent 3239569 (1966).
22. J.L. van Winkle, R.C. Morris, R.F. Mason, US Patent 3420898 (1969).
23. E. Drent, J.C.L.J. Suykerbuyk, US Patent 7186868 B2 (2007).
24. E. Drent, J.C.L.J. Suykerbuyk, US Patent 7208606 B2 (2007).
25. E. Drent, J.C.L.J. Suykerbuyk, US Patent 2007/0032687 A1 (2007).
26. R.D. Garton, J.T. Ritchie, R.F. Caers, US Patent 7081554 B2 (2006).
27. M.J. Lawrenson, Fr. Dem. 1 558 222 (1969).
28. M.J. Lawrenson, G. Foster. Ger. Offen. 1 819 504 (1969).
29. J.M. Vargas, J.A. Hanin, J.C. Reisch, US Patent 5059718 (1991).
30. T. Mackewitz, US Patent 6559344 B2 (2003).
31. MacDougall J.K., Simpson M.C., Green M.J., and Cole-Hamilton D.J. J. Chem. Soc. Dalton Trans. (1996) 1161
32. MacDougall J.K., and Cole-Hamilton D.J. J. Chem. Soc., Chem. Commun. (1990) 165
33. MacDougall J.K., Simpson M.C., and Cole-Hamilton D.J. Polyhedron 12 (1993) 2877
34. MacDougall J.K., Simpson M.C., and Cole-Hamilton D.J. J. Chem. Soc., Dalton Trans. (1994) 3061
35. Cheliatsidou P., White D.F.S., and Cole-Hamilton D.J. Dalton Trans. (2004) 3425
36. Ichihara T., Nakano K., Katayama M., and Nozaki K. Chem. Asian J. 3 (2008) 1722
37. Mizoroki T., Kioka M., Suzuki M., Sakatani S., Okumura A., and Maruya K. Bull. Chem. Soc. Jpn. 57 (1984) 577
38. Konya D., Almeida Leñero K.Q., and Drent E. Organometallics 25 (2006) 3166
39. Haukka M., Alvila L., and Pakkanen T.A. J. Mol. Catal. A: Chem. 102 (1995) 79
40. Evans D., Osborn J.A., and Wilkinson G. J. Chem Soc. A (1968) 3133
41. Izumi Y., Konishi K., Tsukahara M., Obaid D.M., and Aika K. J. Phys. Chem. C 111 (2007) 10073
42. Baird M.C., Nyman C.J., and Wilkinson G. J. Chem. Soc. A (1968) 348
43. Ohno K., and Tsuji J. J. Am. Chem. Soc. 90 (1968) 99
44. Bresler L.S., Buzina N.A., Varshavsky Yu.S., Kiseleva N.V., and Cherkasova T.G. J. Organomet. Chem. 171 (1979) 229
45. Brown C., Heaton B.T., Longhetti L., Povey W.T., and Smith D.O. J. Organomet. Chem. 192 (1980) 93
46. Dougherty T.P., Grubbs W.T., and Heilweil E.J. J. Phys. Chem. 98 (1994) 9396
47. Porta F., Tollari S., Bianchi C., and Recchia S. Inorg. Chim. Acta 249 (1996) 79
48. Collman J.P., and Roper W.R. J. Am. Chem. Soc. 87 (1965) 4008
49. Stephenson T.A., and Wilkinson G. J. Inorg. Nucl. Chem. 28 (1966) 945
50. Krassowski D.W., Nelson J.H., Brower K.R., Hauenstein D., and Jacobson R.A. Inorg. Chem. 27 (1988) 4294
51. Ahmad N., Robinson S.D., and Uttley M.F. J. Chem. Soc. Dalton (1972) 843
52. James B.R., and Markham L.D. Inorg. Nucl. Chem. Lett. 7 (1971) 373
53. Diéguez M., Claver C., Masdeu-Bultó A.M., Ruiz A., van Leeuwen P.W.N.M., and Schoemaker G.C. Organometallics 18 (1999) 2107
54. Brown J.M., Canning L.R., Kent A.G., and Sidebottom P.J. J. Chem. Soc., Chem. Commun. (1982) 721
55. Datt M.S., Nair J.J., and Otto S. Organomet. Chem. 690 (2005) 3422
56. Mieczyńska E., Trzeciak A.M., Grzybek R., and Ziółkowski J.J. J. Mol. Catal. A: Chem. 132 (1998) 203
57. Schulz H.F., and Bellstedt F. Ind. Eng. Chem. Prod. Res. Dev. 12 (1973) 176