Wydział Chemii

Anna M. Trzeciak

Józef J. Ziółkowski

Tadeusz Lis

R. Choukroun

1999

Journal of Organometallic Chemistry

575

87-97

10.1016/S0022-328X(98)00981-4

Naukowa

Angielski

Artykuł

The novel rhodium complexes with the bidentate PO ligand (PO=OC₆H₄PPh₂⁻) of the form Rh(PO)(CO)L (L^a=POH=HOC₆H₄PPh₂ (1), PPh₃ (2), P(NC₄H₄)₃ (4), PPh₂(NC₄H₄) (6)) and Rh(PO)L₂ (L^b=P(OPh)₃ (3), P(NC₄H₄)₃ (5)) were obtained by ligand exchange in Rh(β-diketone)(CO)₂, Rh(β-diketone)(CO)L and Rh(β-diketone)L₂ complexes. All complexes of the Rh(PO)(CO)L^a type exist in solution as isomers with both phosphorus atoms in the trans position as was shown by ³¹P{¹H}-NMR. The trans influence of the phosphorus atom of a bidentate PO ligand is stronger than that of oxygen atom, which is manifested by the differences of Rh–P bonds in (2) (2.283(1) and 2.327(1) Å) and of Rh–P (phosphite) bonds in (3) (2.233(2) and 2.139(2) Å). The complexes (1) and (2) used alone or with an excess of free phosphine (POH, PPh₃, P(NC₄H₄)₃) are not active in hexen-1-e hydroformylation at 1 MPa CO/H₂=1 and at 353 K. The lack of catalytic activity is explained by the extremely high stability of the chelate (PO) ring which does not allow the formation of the active form of the catalyst. In contrast, the complex (3) used alone as the catalyst precursor produces 54 and 72.9% of aldehydes when used with a six-fold excess of P(OPh)₃. Complex (1) modified with P(OPh)₃ catalyses hexen-1-e hydroformylation with a 73.6–84.6% yield of aldehydes. Under hydroformylation reaction conditions, the PO ligand is removed from the coordination sphere of (1) and complexes of the form HRh(CO){P(OPh)₃}₃ and HRh{P(OPh)₃}₄ are formed.

Rhodium complexes, Phosphines, Catalysis, X-ray structure

https://doi.org/10.1016/S0022-328X(98)00981-4

http://www.elsevier.com