How to Deal with Charge in the Ranking of Lewis Acidity: Critical Evaluation of an Extensive Set of Cationic Lewis Acids

被引:14
|
作者
Erdmann, Philipp [1 ]
Schmitt, Manuel [1 ]
Sigmund, Lukas M. [1 ]
Kraemer, Felix [2 ]
Breher, Frank [2 ]
Greb, Lutz [1 ]
机构
[1] Heidelberg Univ, Anorgan Chem Inst, Neuenheimer Feld 270, D-69120 Heidelberg, Germany
[2] Karlsruhe Inst Technol KIT, Inst Inorgan Chem, Engesserstr 15, D-76131 Karlsruhe, Germany
关键词
computational Lewis acidity; fluoride ion affinity; cationic Lewis acids; Lewis acidity scale; p-block elements; SCREENING MODEL; SOLVATION; FLUORIDE; CHEMISTRY;
D O I
10.1002/anie.202403356
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The quantification of Lewis acidity is of fundamental and applied importance in chemistry. However, if neutral and charged Lewis acids are compared, a coherent ranking has been elusive, and severe uncertainties were accepted. With this study, we present a systematic computational analysis of Lewis base affinities of 784 mono-, di- and tricationic Lewis acids and their comparison with 149 representative neutral Lewis acids. Evaluating vacuum fluoride ion affinities (FIA) reveals a charge-caused clustering that prohibits any meaningful ranking. Instead, solvation-corrected FIA(solv) is identified as a metric that overcomes charge sensitivity in a balanced manner, allowing for a coherent evaluation of Lewis acidity across varying charge states. Analyzing the impact of molecular volume on solvation-induced FIA damping provides rationales for fundamental trends and guidelines for the choice or design of neutral and cationic Lewis acids in the condensed phase. Exploring alternative scales, explicit counteranion effects, and selected experimental case studies reaffirms the advantages of solvation-corrected FIA(solv) as the most versatile and practical approach for the quantitative ranking of general (thermodynamic) Lewis acidity.<br />
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页数:8
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