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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis of new thiophenolato hydrido iron(II) complexes and their substitution reactions with alkynes
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Synthesis of new thiophenolato hydrido iron(II) complexes and their substitution reactions with alkynes

机译:新型硫酚基氢化铁(II)配合物的合成及其与炔烃的取代反应

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摘要

The novel thiophenolato hydrido iron(II) complexes [cis-Fe(H)(SAr)(PMe3)4] (4–6) (Ar = p-BrC6H4 (4), p-MeOC6H4 (5) and o-MeC6H4 (6)) were prepared through the reaction of Fe(PMe3)4 with thiophenols ArSH (1–3). Reaction of 6 with trimethylsilylacetylene and phenylacetylene afforded bisalkynyl iron(II) complexes [Fe(PMe3)4(C CSiMe3)2] (7) and [Fe(PMe3)4(C CPh)2] (9) through elimination of dihydrogen and the formation of thiophenol. The reaction of 5 with 2-methyl-3-butyn-2-ol gave [Fe(PMe3)4(C CCMe2OH) 2] (10). The crystal structures of complexes 4, 7 and 10 were determined by X-ray diffraction. A mechanism for the formation of 7 is proposed.
机译:新型硫酚基氢化铁(II)配合物[顺式-Fe(H)(SAr)(PMe3)4](4–6)(Ar = p-BrC6H4(4),p-MeOC6H4(5)和o-MeC6H4( 6))是通过Fe(PMe3)4与硫酚ArSH(1-3)反应制备的。 6与三甲​​基甲硅烷基乙炔和苯乙炔反应,生成双炔基铁(II)配合物[Fe(PMe3)4(C CSiMe3)2](7)和[Fe(PMe3)4(C CPh)2](9)通过消除二氢和形成硫酚。 5与2-甲基-3-丁炔-2-醇的反应得到[Fe(PMe 3)4(C CCMe 2 OH)2](10)。配合物4、7和10的晶体结构通过X射线衍射测定。提出了形成7的机理。

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