Kinetics and mechanisms of homogeneous catalytic reactions: Part 9. Hydroformylation of 1-hexene catalyzed by a rhodium system containing a tridentated phosphine

Abstract

A kinetic study of the homogeneous hydroformylation of 1-hexene to the corresponding aldehydes (heptanal and 2-methyl-hexanal) was carried out by using a rhodium catalyst formed by the addition of 1 equiv. of 1,1,1-tris(diphenylphosphinomethyl)ethane (triphos) to the complex Rh(acac)(CO) 2 under mild reaction conditions (80 °C, 2–10 atm of syn-gas) in toluene; linear to branched ratios ( l/ b) varied from 1.3 to 5.8, depending on the reaction conditions. The reaction rate is first order with respect to the concentration of Rh, fractional order with respect to 1-hexene concentration and zero order with respect to dissolved hydrogen concentration. Increasing the CO pressure up to a threshold value of 2.1 atm accelerates the reaction, further increments inhibit the reaction. Complex RhH(CO)(κ 3-triphos) was isolated and characterized by IR and NMR ( 1H and 31P{H}). The kinetic data and related co-ordination chemistry are consistent with a mechanism involving RhH(CO)(κ 2-triphos) as the active species and the migratory insertion of the alkene into the metal–hydride bond as the rate limiting step. This catalytic cycle is rather similar to that proposed for RhH(CO)(PPh 3) 3 and for RhH(CO) 2(dppe); however, the presence of a triphos ligand co-ordinated in a κ 2 mode through the cycle resulted in l/ b ratio higher than those obtained in systems containing bidentated phosphines.