Hamilton Hugh B, King Ashley M, Sparkes Hazel A, Pridmore Natalie E, Wass Duncan F
School of Chemistry , University of Bristol , Cantock's Close, Bristol , BS8 1TS , United Kingdom.
Cardiff Catalysis Institute, School of Chemistry , Cardiff University , Main Building, Park Place , Cardiff , CF10 3AT , United Kingdom.
Inorg Chem. 2019 May 6;58(9):6399-6409. doi: 10.1021/acs.inorgchem.9b00569. Epub 2019 Apr 24.
A series of intermolecular transition metal frustrated Lewis pairs (FLPs) based on zirconocene alkoxide complexes ([CpZr(OMes)] 1 or ([Cp*Zr(OMes)] 2) with nitrogen Lewis bases (NEt, NEtPr, pyridine, 2-methylpyridine, 2,6-lutidine) are reported. The interaction between Zr and N depends on the specific derivatives used, in general more sterically encumbered pairs leading to a more frustrated interaction; however, DOSY NMR spectroscopy reveals these interactions to be dynamic in nature. The pairs undergo typical FLP-type reactivity with D, CO, THF, and PhCCD. The catalytic dehydrocoupling of MeNH·BH is also reported. Comparisons can be made with previous work employing phosphines as Lewis bases suggesting that hard-hard or hard-soft acid-base considerations are of little importance compared to the more prominent roles of steric bulk and basicity.
报道了一系列基于锆茂醇盐配合物([CpZr(OMes)] 1或([Cp*Zr(OMes)] 2)与氮路易斯碱(NEt、NEtPr、吡啶、2-甲基吡啶、2,6-二甲基吡啶)的分子间过渡金属受阻路易斯对(FLP)。Zr与N之间的相互作用取决于所使用的特定衍生物,一般来说,空间位阻更大的对导致更受阻的相互作用;然而,扩散排序核磁共振光谱(DOSY NMR)表明这些相互作用本质上是动态的。这些对与D、CO、THF和PhCCD发生典型的FLP型反应。还报道了MeNH·BH的催化脱氢偶联反应。可以与以前使用膦作为路易斯碱的工作进行比较,这表明与空间位阻和碱性的更突出作用相比,硬-硬或硬-软酸碱考虑不太重要。