首页> 外文期刊>Journal of the American Chemical Society >Derivatization of Phosphine Ligands with Bulky Deltahedral Zintl Clusters - Synthesis of Charge Neutral Zwitterionic Tetrel Cluster Compounds [(Ge_9{Si(TMS)_3}_2)~tBu_2P]M(NHC~(Dipp)) (M: Cu, Ag, Au)
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Derivatization of Phosphine Ligands with Bulky Deltahedral Zintl Clusters - Synthesis of Charge Neutral Zwitterionic Tetrel Cluster Compounds [(Ge_9{Si(TMS)_3}_2)~tBu_2P]M(NHC~(Dipp)) (M: Cu, Ag, Au)

机译:庞大的四面体Zintl团簇衍生化膦配体-电荷中性两性离子三价铁簇簇化合物[(Ge_9 {Si(TMS)_3} _2)〜tBu_2P] M(NHC〜(Dipp))(M:Cu,Ag,Au)的合成

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摘要

Reactions of silylated clusters [Ge_9{Si(TMS)_3}_3]~- or [Ge_9{Si(TMS)_3}_2]~(2-) with dialkylhalophosphines R_2PCl (Cy, ~iPr, ~tBu) at ambient temperature yield the first tetrel Zintl cluster compounds bearing phosphine moieties. Varying reactivity of the dialkylhalophosphines toward the silylated clusters is observed depending on the bulkiness of the phosphine's alkyl substituents and on the number of hypersilyl groups at the tetrel cluster. Reactions between phosphines with small cyclohexyl- (Cy) or isopropyl- (~iPr) groups and the tris-silylated cluster [Ge_9{Si(TMS)_3}_3]~- yield the novel neutral cluster compounds [Ge_9{Si(TMS)_3}_3PR_2] (R: Cy (1), ~iPr (2)) with discrete Ge-P exo bonds. By contrast, the bulkier phosphine ~tBu_2PCl does not react with [Ge_9{Si(TMS)_3}_3]~- due to steric crowding. However, the reaction with the bis-silylated cluster [Ge_9{Si(TMS)_3}_2]~2 ~- yields the novel cluster compound [Ge_9{Si(TMS)_3}_2P~tBu_2]~- (3). Subsequent reactions of compound 3 with NHC~(Dipp)MCl (M: Cu, Ag, Au) yield the charge neutral zwitterionic compounds [(Ge_9{Si(TMS)_3}_2)~tBu_2P]M(NHC~(Dipp)) (M: Cu, Ag, Au) (4-6), in which compound 3 acts as a phosphine ligand bearing a bulky tetrel Zintl cluster moiety. Compounds 4-6 also represent the first uncharged examples for 3-fold substituted tetrel Zintl clusters.
机译:甲硅烷基化簇[Ge_9 {Si(TMS)_3} _3]〜-或[Ge_9 {Si(TMS)_3} _2]〜(2-)与二烷基卤代膦R_2PCl(Cy,〜iPr,〜tBu)在室温下的反应第一个具有膦部分的锡特尔Zintl簇化合物。观察到二烷基卤代膦酸酯对甲硅烷基化簇的反应性不同,这取决于膦烷基取代基的体积和在蝶形簇上的高甲硅烷基的数目。具有小的环己基-(Cy)或异丙基-(〜iPr)基团的膦与三甲硅烷基化的簇[Ge_9 {Si(TMS)_3} _3]〜-之间的反应产生新型中性簇化合物[Ge_9 {Si(TMS) _3} _3PR_2](R:Cy(1),〜iPr(2))具有离散的Ge-P外键。相反,由于空间拥挤,较大的膦〜tBu_2PC1不与[Ge_9 {Si(TMS)_3} _3]〜反应。然而,与双甲硅烷基化簇[Ge_9 {Si(TMS)_3} _2] _2 ~~的反应产生了新型簇化合物[Ge_9 {Si(TMS)_3} _2P〜tBu_2]〜-(3)。化合物3与NHC〜(Dipp)MCl(M:Cu,Ag,Au)的后续反应产生电荷中性的两性离子化合物[(Ge_9 {Si(TMS)_3} _2)〜tBu_2P] M(NHC〜(Dipp)) (M:Cu,Ag,Au)(4-6),其中化合物3充当带有庞大的锡特尔Zintl簇部分的膦配体。化合物4-6也代表了3倍取代的蝶形Zintl簇的第一个不带电荷的实例。

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  • 来源
    《Journal of the American Chemical Society》 |2017年第34期|11933-11940|共8页
  • 作者单位

    Department of Chemistry, Technical University of Munich, Lichtenbergstraße 4, Garching, Germany,WACKER Institute for Silicon Chemistry, Lichtenbergstraße 4, Garching, Germany;

    Department of Chemistry, Technical University of Munich, Lichtenbergstraße 4, Garching, Germany;

    Department of Chemistry, Technical University of Munich, Lichtenbergstraße 4, Garching, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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