Amb. Osuna et al., Effects of the ponytails of arylphosphines on the hydroformylation of higher olefins in supercritical CO2, J CHEM S DA, (22), 2000, pp. 4052-4055
Citations number
40
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
A series of ponytail-appended arylphosphines P(C6H4R-m)(3) (m=4, R=n-C6F13
1, n-CH2CH2C6F13 3, n-C6H13 4, n-C10H21 5 or n-C16H33 6; m=3, R=n-C6F13 2)
have been studied in the rhodium-catalysed hydroformylation of higher olefi
ns in supercritical CO2 (scCO(2)), with the perfluoroalkylated ligands exhi
biting the highest and the alkylated one the lowest activities. The high ra
tes derived from 1 and 2 probably originate from the strong electron-withdr
awing effect of their ponytails, while the slow rates observed with 4-6 are
mainly due to the low solubility of these ligands in scCO(2).