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Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids

机译:四方磷(v)阳离子是可调节且坚固的催化路易斯酸

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摘要

The synthesis and catalytic reactivity of a class of water-tolerant cationic phosphorus-based Lewis acids is reported. Corrole-based phosphorus(v) cations of the type [ArP(cor)][B(C6F5)4] (Ar = C6H5, 3,5-(CF3)2C6H3; cor = 5,10,15-(C6H5)3corrolato3–, 5,10,15-(C6F5)3corrolato3–) were synthesized and characterized by NMR and X-ray diffraction. The visible electronic absorption spectra of these cationic phosphacorroles depend strongly on the coordination environment at phosphorus, and their Lewis acidities are quantified by spectrophotometric titrations. DFT analyses establish that the character of the P-acceptor orbital comprises P–N antibonding interactions in the basal plane of the phosphacorrole. Consequently, the cationic phosphacorroles display unprecedented stability to water and alcohols while remaining highly active and robust Lewis acid catalysts for carbonyl hydrosilylation, Csp3–H bond functionalization, and carbohydrate deoxygenation reactions.
机译:报道了一类耐水阳离子磷基路易斯酸的合成和催化反应性。 [ArP(cor)] [B(C6F5)4]类型的基于Corrole的磷(v)阳离子(Ar = C6H5,3,5-(CF3)2C6H3; cor = 5,10,15-(C6H5)3corrolato合成了 3 – ,5,10,15-(C6F5)3corrolato 3 ),并通过NMR和X射线衍射对其进行了表征。这些阳离子性磷酰基酚的可见电子吸收光谱在很大程度上取决于磷的配位环境,其路易斯酸度通过分光光度滴定法定量。 DFT分析确定,P受体轨道的特征在磷aco子的基面上包含P–N反键相互作用。因此,阳离子膦酸对水和醇显示出空前的稳定性,同时仍保持高活性和稳健的路易斯酸催化剂用于羰基氢化硅烷化,Csp 3 -H键官能化和碳水化合物脱氧反应。

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