Rhodium catalysts bound to functionalized mesoporous silica
Phosphine and amine functionalized mesoporous silica materials were metallated with Rh(CO)2(i-Pr2NH)Cl or Rh2(CO)4Cl2, respectively, to yield catalysts containing the Rh(PPh2R)2(CO)Cl or Rh(CO)2(NH2R)Cl, where R is a propyl chain bonded to the silica surface, reactive centers. In order to ascertain the effect of pore size on rates of hydroformylation catalysis both 35 and 45 ? pore size materials were used. Using the hydroformylation of octene as a reference reaction, the phosphine based, 45 ? catalysts were 1.5-1.3 times faster than the amine based, 45 ? materials were 2.6-2.1 times faster than the 35 ? catalysts, and the 45 ? materials. The orientation of the catalyst relative to the functionalized surface, and the steric environment around the catalyst active site appear to be significant in determining rate of reaction. The ability of the surface bound phosphine catalysts to affect hydroformylation was strongly influenced by the steric constraints of the substrate. Terminal alkenes were readily hydroformylated and norbornene was slowly hydroformylated, but pinene, trans-cyclododecene, cyclohexene and cholesterol were nonreactive to the catalytic center.
- Research Organization:
- Pacific Northwest National Laboratory (PNNL), Richland, WA (US)
- Sponsoring Organization:
- USDOE
- DOE Contract Number:
- AC05-76RL01830
- OSTI ID:
- 860054
- Report Number(s):
- PNNL-SA-43062; KP1301020
- Journal Information:
- Inorganica Chimica Acta, Journal Name: Inorganica Chimica Acta Journal Issue: 10 Vol. 357; ISSN 0020-1693; ISSN ICHAA3
- Country of Publication:
- United States
- Language:
- English
Similar Records
Hydroformylation catalyzed by immobilized rhodium complex to polymer support
Titania-silica mixed oxides. II. Catalytic behaviour in olefin epoxidation