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Can the Lewis Basicity of an Isolated Solvent Molecule be Used for Characterizing Solvent Effects?

Author(s): Jean-François Gal* and Pierre-Charles Maria

Volume 17, Issue 3, 2021

Published on: 07 June, 2020

Page: [328 - 338] Pages: 11

DOI: 10.2174/1573411016999200607171803

Price: $65

Abstract

Background: The ubiquitous Lewis acid/base interactions are important in solution processes. Analytical chemistry may benefit from a better understanding of the role of Lewis basicity at the molecular level or acting through a bulk solvent effect.

Objective: To delineate (i) the basicity at a molecular level, hereafter referred to as solute basicity, and (ii) the solvent basicity, which is a bulk-liquid property.

Methods: The literature that relates Lewis basicity scales and solvent effects is analyzed. A special focus is placed on two extensive scales, the Donor Number, DN, and the BF3 Affinity scale, BF3A, which were obtained by calorimetric measurements on molecules as solutes diluted in a quasi-inert solvent, and therefore define a molecular Lewis basicity. We discuss the validity of these solute scales when regarded as solvent scales, in particular when the basicity of strongly associated liquids is concerned.

Results: We demonstrate the drawbacks of confusing the Lewis basicity of a solvent molecule, isolated as a solute, and that of the bulk liquid solvent itself.

Conclusion: Consequently, we recommend a reasoned use of the concept of Lewis basicity taking clearly into account the specificity of the process for which a Lewis basicity effect may be invoked. In particular, the action of the Lewis base, either as an isolated entity or as a bulk liquid, must be distinguished.

Keywords: Donicity, donor number, lewis basicity, solute basicity, solvent basicity, solvent effects, trifluoroborane (boron trifluoride).

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