Abstract

It is shown that phosphinooxazolines such as (2-oxazoline-2-ylmethyl)diphenylphosphine 1 can be used as P,N assembling ligands for the synthesis of heterometallic complexes. These were obtained in a stepwise manner from the iron carbonyl complexes containing one, [Fe(CO)4(PCH2-oxazoline-P)] 2, or two, trans-[Fe(CO)3(PCH2-oxazoline-P)2] 6, P-bound phosphinooxazoline ligands. These metalloligands were then reacted with metal complexes. With 2, complete ligand transfer from Fe to the second metal (Pd) was sometimes observed. The metal–metal bonded complex [(OC)4Fe(μ-PCH2-oxazoline-P,N)PdCl2] 3 was of limited stability, whereas the trinuclear complex trans-[{(OC)4Fe(μ-PCH2-oxazoline-P,N)}2CoCl2] 4, in which 2 functions as a N-donor metalloligand toward the tetrahedral Co(II) centre, was stable and could be fully characterised by X-ray diffraction. This complex catalyses the oligomerization of ethylene to give linear α-olefins in the range C4–C26, with a maximum of the Schulz-Flory distribution around C6. The complex [{(OC)4Fe(μ-PCH2-oxazoline-P,N)}2HgI2] 5 was also prepared from 6. With the metalloligand 6, the Fe→Pd and Fe→Co metal–metal bonded compounds trans-[(OC)3Fe(μ-PCH2-oxazoline-P,N)2Pd(NCMe)](BF4)28 and trans-[(OC)3Fe(μ-PCH2-oxazoline-P,N)2CoCl2] 9 were obtained.

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