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Experimental and Computational Gas Phase Acidities of Conjugate Acids of Triazolylidene Carbenes: Rationalizing Subtle Electronic Effects

机译:实验和计算气相酸的三唑基碳烯共轭酸:合理化微妙的电子效应。

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摘要

In recent years, triazolylidene carbenes have come to the forefront as important organocatalysts for a wide range of reactions. The fundamental properties of these species, however, remain largely unknown. Herein, the gas phase acidities have been measured and calculated for a series of triazolium cations (the conjugate acids of the triazolylidene carbenes) that have not been heretofore examined in vacuo. The results are discussed in the context of these species as catalysts. We find correlations between the gas phase acidity and selectivity in two Umpolung reactions catalyzed by these species; such correlations are the first of their kind. We are able to use these linear correlations to improve reaction enantioselectivity. These results establish the possibility of using these thermochemical properties to predict reactivity in related transformations.
机译:近年来,三唑基碳烯作为最重要的有机催化剂,已广泛用于各种反应中。但是,这些物种的基本特性仍然未知。在此,已经测量和计算了迄今为止尚未在真空中检查的一系列三唑鎓阳离子(三唑基卡宾的共轭酸)的气相酸度。在这些物质作为催化剂的背景下讨论了结果。我们发现在由这些物种催化的两个Umpolung反应中,气相酸度与选择性之间存在相关性。这种相关性尚属首次。我们能够使用这些线性相关性来提高反应对映选择性。这些结果建立了使用这些热化学性质来预测相关转化中的反应性的可能性。

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