School of Chemistry, University of Bristol , Cantock's Close, Bristol BS8 1TS, United Kingdom.
J Am Chem Soc. 2016 Feb 17;138(6):1994-2003. doi: 10.1021/jacs.5b12536. Epub 2016 Feb 4.
We report intermolecular transition metal frustrated Lewis pairs (FLPs) based on zirconocene aryloxide and phosphine moieties that exhibit a broad range of small molecule activation chemistry that has previously been the preserve of only intramolecular pairs. Reactions with D2, CO2, THF, and PhCCH are reported. By contrast with previous intramolecular examples, these systems allow facile access to a variety of steric and electronic characteristics at the Lewis acidic and Lewis basic components, with the three-step syntheses of 10 new intermolecular transition metal FLPs being reported. Systematic variation to the phosphine Lewis base is used to unravel steric considerations, with the surprising conclusion that phosphines with relatively small Tolman steric parameters not only give highly reactive FLPs but are often seen to have the highest selectivity for the desired product. DOSY NMR spectroscopic studies on these systems reveal for the first time the nature of the Lewis acid/Lewis base interactions in transition metal FLPs of this type.
我们报告了基于锆氧芳基和膦部分的分子间过渡金属受阻路易斯对(FLP),它们表现出广泛的小分子活化化学,以前只有分子内对才能实现。报道了与 D2、CO2、THF 和 PhCCH 的反应。与以前的分子内实例相比,这些体系允许在路易斯酸和路易斯碱组分上轻松获得各种空间和电子特性,报道了 10 个新的分子间过渡金属 FLP 的三步合成。系统地改变膦路易斯碱以揭示空间考虑因素,令人惊讶的结论是,具有相对较小的 Tolman 空间参数的膦不仅给出了高反应性的 FLP,而且通常对所需产物具有最高的选择性。这些体系的 DOSY NMR 光谱研究首次揭示了这种类型的过渡金属 FLP 中路易斯酸/路易斯碱相互作用的性质。