| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1324545 | Journal of Organometallic Chemistry | 2011 | 4 Pages |
The diiron complex [Fe2{μ-к1(O):η1(C):η3(C)–C(N(Me)(Xyl))C(H)C(Me)C(O)OMe}(μ-CO)(Cp)2] (2) has been obtained from the diiron bridging vinyliminium [Fe2{μ-η1:η3–C(Me)C(H)CN(Me)(Xyl)}(μ-CO)(CO)(Cp)2][SO3CF3] (1; Xyl = 2,5-C6H3Me2) upon treatment with NaH in the presence of CH2CCMe2, followed by chromatography on alumina with MeOH as eluent. The reaction consists in the incorporation of a methylcarboxylate unit, assembled from CO and MeO−, into the bridging vinyliminium ligand. The resulting complex 2 exhibits a C4 fragment bridging the two iron centres through the carbonyl oxygen atom and the allylidene moiety.The X-ray molecular structure of 2 has been determined.
Graphical abstractThe bridging vinyliminium ligand, in a diiron complex, undergoes incorporation of a methycarboxylate group, generated from a CO ligand and MeOH. The resulting frame exhibits an unprecedented coordination mode, bridging the two Fe atoms through the carbonyl oxygen and the allylidene moiety .Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► C–C and C–H bond formation promoted by diiron complexes. ► Assembly and incorporation of a CO2Me group into a bridging ligand. ► Transformation bridging vinyliminium ligands in diiron complexes.
