Department of Chemistry , University of California , One Shields Avenue , Davis , California 95616 , United States.
J Org Chem. 2019 Dec 20;84(24):15845-15853. doi: 10.1021/acs.joc.9b02107. Epub 2019 Dec 11.
The relative Lewis acidity of a variety of metal-ligand catalyst complexes is quantified using P NMR spectroscopy. Three P NMR probes, including two new bidentate binding probes, are compared on the basis of different binding modes (i.e., monodentate vs bidentate) and the relative scale of their downfield shift upon binding to Lewis acid complexes. Bidentate coordination of catalyst complexes including metal catalysts, ligands, and counterions were assessed due to their importance to asymmetric catalysis. The effect of ligands, counterions, and additives on Lewis acidity is quantified and correlated to reaction yield at an early time point as an approximation for catalytic activity/efficiency and chelation mode in two organic transformations. Binding studies were performed under catalytically relevant conditions, giving further applicability to synthesis. Insight into activation modes are revealed through this analysis.
采用 P NMR 光谱法对多种金属-配体催化剂配合物的相对路易斯酸度进行定量分析。基于不同的结合模式(即单齿配位与双齿配位)以及与路易斯酸配合物结合时的场移相对幅度,比较了三种 P NMR 探针,其中包括两种新的双齿结合探针。由于双齿配位对于不对称催化具有重要意义,因此评估了包括金属催化剂、配体和抗衡离子在内的催化剂配合物的双齿配位。定量研究了配体、抗衡离子和添加剂对路易斯酸度的影响,并将其与两个有机转化中早期的反应产率相关联,以作为对催化活性/效率和螯合模式的近似值。结合研究在催化相关条件下进行,从而进一步适用于合成。通过该分析揭示了对活化模式的深入了解。