4.8 Article

Compensation of London Dispersion in the Gas Phase and in Aprotic Solvents

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 40, Pages 14281-14288

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201905436

Keywords

aprotic solvents; dispersion forces; molecular recognition; non-covalent interactions; solvent effects

Funding

  1. ETH Zurich
  2. Schweizerischer Nationalfonds
  3. Deutsche Forschungsgemeinschaft [SPP1807]
  4. ACS Petroleum Research Fund

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The importance of London dispersion for structure and stability of molecules with less than about 200 atoms has been established in recent years but the quantitative understanding is still largely based on computations because of a persistent lack of suitable experimental data. We herein report a comprehensive computational and experimental study of the compensation of London dispersion in proton-bound dimer dissociations showing that total compensation is largely invariant in both polar and nonpolar aprotic solvents spanning a wide range of bulk polarizabilities. Additionally, we find that compensation by solvent (which is about 40-80 %) largely dominates over compensation in the gas phase (which is about 0-40 %) for typical experimental temperatures.

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