1-Dodecene hydroformylation catalyzed by water-soluble rhodium complex, RhC
1(CO)(TPPTS)(2) [TPPTS: P(m-C6H4SO3Na)(3)], in the presence of surfactants
and alcoholic solvents was studied. The results indicated that the hydrofor
mylation in biphasic catalytic system occurred in the interface of aqueous/
organic phases. The formation of micelle was not only favorable for the rea
ction acceleration, but also favorable for the increase of linear aldehyde
ratio in products. The key factor of the enhancement of reaction rate was t
he richness of rhodium catalyst in the interlayer with the static electrici
ty attraction between active rhodium anion species and cationic end of surf
actant. (C) 1999 Elsevier Science B.V. All rights reserved.