A new concept of tethered ligand-modified Rh/SiO2 catalyst for hydroformylation with high stability

Applied Catalysis A: General

Volumn 353, Issue 2, 2009, Pages 266-270

  Li, Xianming ^a,b   Ding, Yunjie ^a   Jiao, Guiping ^a,b   Li, Jingwei ^a,b   Lin, Ronghe ^a,b   Gong, Leifeng ^a,b   Yan, Li ^a   Zhu, Hejun ^a  

^a DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Hydroformylation; Rh SiO2 catalyst; Tethered ligand

Indexed keywords

AVIATION; CATALYSIS; COORDINATION REACTIONS; ETHYLENE; FOURIER TRANSFORM INFRARED SPECTROSCOPY; HYDROFORMYLATION; HYDROXYLATION; LEACHING; METALS; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SILICON COMPOUNDS;

ACTIVE SPECIES; FLEXIBLE LIGANDS; HIGH ACTIVITIES; HIGH STABILITIES; IN-SITU; METAL PARTICLES; NEW CONCEPTS; ORGANIC LIGANDS; PROBE REACTIONS; RH/SIO2 CATALYST; TETHERED LIGAND;

LIGANDS;

EID: 58149199534     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2008.10.052     Document Type: Article

References (18)

1. van Koten G., and van Leeuwen P.W.N.M. In: Delmon B., and Yates J.T. (Eds). Studies in Surface Science and Catalysis vol. 123 (1999), Elsevier, Amsterdam 289-342 (ch. 6)
2. Hodnett B.K., Janssen F.J.J.G., Niemantsverdriet J.W., Ponec V., van Santen R.A., and van Veen J.A.R. In: Delmon B., and Yates J.T. (Eds). Studies in Surface Science and Catalysis vol. 123 (1999), Elsevier, Amsterdam 209-287 (ch. 5)
3. Ichikawa M., Lang A.J., Shriver D.F., and Sachtler W.M.H. J. Am. Chem. Soc. 107 (1985) 7216-7218
4. Naito S., and Tanimoto M. J. Chem. Soc., Chem. Commun. (1989) 1403-1404
5. Izumi Y., Asakura K., and Iwasawa Y. J. Catal. 132 (1991) 556-570
6. Feng X., Fryxell G.E., Wang L.Q., Kim A.Y., Liu J., and Kemner K.M. Science 276 (1997) 923-926
7. Li H., Zhang F., Wan Y., and Lu Y. J. Phys. Chem. B 110 (2006) 22942-22946
8. Chiang C.-L., Chang R.-C., and Chiu Y.-C. Thermochim. Acta 453 (2007) 97-104
9. Gao H., and Angelici R.J. J. Mol. Catal. A: Chem. 145 (1999) 83-94
10. Mastrorilli P., and Nobile C.F. Coord. Chem. Rev. 248 (2004) 377-395
11. Dasgupta M., Peori M.B., and Kakkar A.K. Coord. Chem. Rev. 233 (2002) 223-235
12. Michalska Z.M., Rogalski Ł., Rózga-Wijas K., Chojnowski J., Fortuniak W., and Ścibiorek M. J. Mol. Catal. A: Chem. 208 (2004) 187-194
13. Jones C.W., McKittrick M.W., Nguyen J.V., and Yu K. Top. Catal. 34 (2005) 67-76
14. Bilhou J.L., Bilhou-Bougnol V., and Graydon W.F. J. Organomet. Chem. 153 (1978) 73-84
15. Yan L., Ding Y.J., Zhu H.J., Xiong J.M., Wang T., Pan Z.D., and Lin L.W. J. Mol. Catal. A: Chem. 234 (2005) 1-7
16. Zhu H.J., Ding Y.J., Yan L., Lu Y., Li C., Bao X.H., and Lin L.W. Chem. Lett. 33 (2004) 630-631
17. Zhu H.J., Ding Y.J., Yan L., Xiong J.M., Lu Y., and Lin L.W. Catal. Today 93-95 (2004) 389-393
18. Yang A.C., and Garland C.W. J. Phys. Chem. 61 (1957) 1504-1512