Adding Diversity to Diiron Aminocarbyne Complexes with Amine Ligands
نویسندگان
چکیده
The reactions of the diiron aminocarbyne complexes [Fe2Cp2(NCMe)(CO)(μ-CO){μ-CN(Me)(R)}]CF3SO3 (R = Me, 1aNCMe; R Cy, 1bNCMe), freshly prepared from tricarbonyl precursors 1a–b, with primary amines containing an additional function (i.e., alcohol or ether) proceeded replacement labile acetonitrile ligand and formation [Fe2Cp2(NH2CH2CH2OR’)(CO)(μ-CO){μ-CN(Me)(R)}]CF3SO3 R’ H, 2a; 2b; 2c) in 81–95% yields. diiron-oxazolidinone conjugate [Fe2Cp2(NH2OX)(CO)(μ-CO){μ-CN(Me)2}]CF3SO3, 3, was 1a, 3-(2-aminoethyl)-5-phenyloxazolidin-2-one (NH2OX) Me3NO, finally isolated 96% yield. In contrast, one pot 1a-b NHEt2 presence Me3NO gave unstable [Fe2Cp2(NHEt2)(CO)(μ-CO){μ-CN(Me)(R)}]CF3SO3 4a; 4b) as unclean products. All were characterized by analytical spectroscopic techniques; moreover, behavior 2a–c 3 aqueous media ascertained.
منابع مشابه
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ژورنال
عنوان ژورنال: Inorganics (Basel)
سال: 2023
ISSN: ['2304-6740']
DOI: https://doi.org/10.3390/inorganics11030091