Hydroformylation in reverse micellar systems

Different micellar systems are characterized. Hydroformylation reactions are carried out in the most appropriate ones and are compared with hydroformylations in a non-micellar system. Reaction rates and selectivities for aldehydes are higher than the micelles. In addn. to this, olefins between C6 and C16 are successfully hydroformylated in the micellar system, whereas C8 is the highest olefin that can be hydroformylated without micelles. The behavior of the reaction in the micellar system is very sensitive to the initial compn. and reaction conditions. [on SciFinder (R)]


Published in:
Catalysis Today, 48, 1-4, 237-243
Year:
1999
ISSN:
0920-5861
Keywords:
Note:
CAN 130:224558
45-1
Industrial Organic Chemicals, Leather, Fats, and Waxes
Swiss Federal Institute of Technology Lausanne (EPFL),Lausanne,Switz.
Journal
written in English.
Laboratories:


Note: The status of this file is: Anyone


 Record created 2006-04-18, last modified 2020-10-26

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