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U.S. Department of Energy
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Hydroformylation of 1-heptene catalyzed by ruthenium cluster

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OSTI ID:43270
; ;  [1]
  1. Taiyuan Univ. of Technology (China). Inst. of Coal Chemical Engineering
Hydroformylation of 1-heptane catalyzed by homogeneous and heterogeneous Ru{sub 3}(CO){sub 12} catalyst has been investigated. Ru{sub 3}(CO){sub 12} has almost no activity when reaction temperature is below 60 C, and nearly stable activity when over 100 C. The maximum selectivity to aldehyde is obtained at 120 C and N/I values of aldehyde and alcohol decrease rapidly with temperature increase. Supported Ru{sub 3}(CO){sub 12} catalyst modified with NaBH{sub 4} or KOH has higher catalytic activity and selectivity to aldehyde in heterogeneous catalysis. Compared with supported Ru{sub 3}(CO){sub 12} catalyst modified with NaBH{sub 4} or KOH has higher catalytic activity and selectivity to aldehyde in heterogeneous catalysis. Compared with supported Ru{sub 3}(CO){sub 12} catalysts, Ru{sub 3}(CO){sub 12}/Co{sub 2}(CO){sub 8}/{gamma}-Al{sub 2}O{sub 3} has high activity and selectivity. When PPh{sub 3} or (NEt{sub 4}) Cl is added to the reaction system, the selectivity to aldehyde and N/I increase. The FTIR spectra of catalysts after reaction show that Ru{sub 3}(CO){sub 12} and Co{sub 2}(CO){sub 8} are changed to new carbonyl complexes which may have catalytic activity.
OSTI ID:
43270
Report Number(s):
CONF-940930--
Country of Publication:
United States
Language:
English