Abstract

It is well-known that the liquid-phase homogeneous unmodified rhodium-catalyzed hydroformylation of alkenes is irreversibly poisoned by the presence of trace quantities of alkynes. In the present contribution, we examined the reaction of four series of monosubstituted and disubstituted alkynes (20 compounds) with Rh4(CO)12 in n-hexane solvent at 293 K under both (A) 2.0 MPa CO and (B) 2.0 MPa CO and 2.0 MPa H2. The analytic method used was in-situ high-pressure infrared spectroscopy. It was observed that (I) all alkynes used in this study reacted quantitative with Rh4(CO)12 in a matter of hours, (II) the final spectra were not influenced by the presence of hydrogen, (III) the monosubstituted alkynes consistently gave a final product involving six terminal νCO vibrations in the region 2036−2121 cm-1 and two vibrations at ca. 1668 and 1689 cm-1, and (IV) the disubstituted alkynes consistently gave a final spectrum consistent with the superposition of the spectra obtained in III plus a spectrum involving fiv...

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