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Coupling of Allenes with μ‐Alkylidyne Ligands in Diiron Complexes: Synthesis of Novel Bridging Thio‐ and Aminobutadienylidene Complexes
18
Citations
40
References
2008
Year
Diiron Aminocarbyne ComplexesInorganic ChemistryEngineeringDiiron ComplexesBiochemistryNatural SciencesCoordination ComplexOrganometallic CatalysisMolecular ComplexChemistryNovel Bridging Thio‐Cf 3μ‐Alkylidyne LigandsFe 2Inorganic SynthesisBiomolecular EngineeringInorganic Compound
Abstract The diiron aminocarbyne complexes [Fe 2 {μ‐CN(Me)(R)}(μ‐CO)(CO) 2 (Cp) 2 ][SO 3 CF 3 ] (R = Xyl, 1a ; R = 4‐C 6 H 4 OMe, 1b ; R = Me, 1c ; Xyl = 2,6‐Me 2 C 6 H 3 ) react with allenes of the type CH 2 =C=CR′R″, in the presence of Me 3 NO/Et 3 N, to give the novel butadienylidene complexes [Fe 2 {μ‐η 1 :η 3 ‐C α N(R)(Me)C β (H)C γ C δ (R′)(R″)}(μ‐CO)(CO)(Cp) 2 ] (R = Xyl, R′ = R″ = Me, 3a ; R = Xyl, R′ = Me, R″ = H, 3b ; R = Xyl, R′ = CO 2 Et, R″ = H, 3c ; R = 4‐C 6 H 4 OMe, R′ = CO 2 Et, R″ = H, 3d ; R = R′ = R″ = Me, 3e ; R = Me, R′ = CO 2 Et, R″ = H, 3f ) in high yields. Analogously, the diiron thiocarbyne complex [Fe 2 (μ‐CSMe)(μ‐CO)(CO) 2 (Cp) 2 ][SO 3 CF 3 ] ( 2 ) reacts with CH 2 =C=CR′R″, in the presence of Me 3 NO/Et 3 N, to afford the compounds[Fe 2 {μ‐η 1 :η 3 ‐C α S(Me)C β (H)C γ C δ (R′)(R″)}(μ‐CO)(CO)(Cp) 2 ](R′ = R″ = Me, 4a ; R′ = CO 2 Et, R″ = H, 4b ; R′ = SiMe 3 , R″ = Me, 4c ). Complexes 3 – 4 exist in solution as mixtures of cis and trans isomers. Compounds 3a and 3e , upon treatment with HSO 3 CF 3 , are transformed into the corresponding vinyliminium complexes [Fe 2 {μ‐η 1 :η 3 ‐C γ (C δ HMe 2 )C β HC α N(R)(Me)}(μ‐CO)(CO)(Cp) 2 ][SO 3 CF 3 ] (R = Xyl, 5a ; R = Me, 5b ), in nearly quantitative yields. Conversely, compounds 4a , b undergo methylation (by CH 3 SO 3 CF 3 ) at the sulfur to give the cationic complexes [Fe 2 {μ‐η 1 :η 3 ‐C α (SMe 2 )C β (H)C γ C δ (R′)(R″)}(μ‐CO)(CO)(Cp) 2 ][SO 3 CF 3 ] (R′ = R″ = Me, 7a ; R′ = CO 2 Et, R″ = H, 7b ). Protonation of 3a is not reversible: treating 5a with sodium hydride results in the formation of the 1‐metalla‐2‐amino‐cyclopenta‐1,3‐dien‐5‐one species [Fe(Cp)(CO){CN(Me)(Xyl)CHC(CHMe 2 )C(O)}] ( 6 ). The molecular structures of cis ‐ 3a , cis ‐ 4b , 5a [CF 3 SO 3 ]·CH 2 Cl 2 and 7a [CF 3 SO 3 ]·0.5CH 2 Cl 2 have been determined by X‐ray diffraction studies. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
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