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Superalkali-Alkalide Interactions and Ion Pairing in Low-Polarity Solvents.
Riedel, René; Seel, Andrew G; Malko, Daniel; Miller, Daniel P; Sperling, Brendan T; Choi, Heungjae; Headen, Thomas F; Zurek, Eva; Porch, Adrian; Kucernak, Anthony; Pyper, Nicholas C; Edwards, Peter P; Barrett, Anthony G M.
Afiliação
  • Riedel R; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, Wood Lane, London W12 0BZ, U.K.
  • Seel AG; Department of Physics and Astronomy, University College London, Gower Street, London WC1E 6BT, U.K.
  • Malko D; Inorganic Chemistry Laboratories, University of Oxford, Park Royal Road, Oxford OX1 3QR, U.K.
  • Miller DP; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, Wood Lane, London W12 0BZ, U.K.
  • Sperling BT; Department of Chemistry, Hofstra University, 106 Berliner Hall, Hempstead, New York 11549, United States.
  • Choi H; Department of Chemistry, Hofstra University, 106 Berliner Hall, Hempstead, New York 11549, United States.
  • Headen TF; School of Engineering, Cardiff University, Cardiff CF24 3AA, U.K.
  • Zurek E; ISIS Neutron and Muon Source, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Campus, Didcot OX11 0QX, U.K.
  • Porch A; Department of Chemistry, State University of New York at Buffalo, 777 Natural Sciences Complex, Buffalo, New York 14260-3000, United States.
  • Kucernak A; School of Engineering, Cardiff University, Cardiff CF24 3AA, U.K.
  • Pyper NC; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, Wood Lane, London W12 0BZ, U.K.
  • Edwards PP; University Chemical Laboratory, Lensfield Road, Cambridge CB2 1EW, U.K.
  • Barrett AGM; Inorganic Chemistry Laboratories, University of Oxford, Park Royal Road, Oxford OX1 3QR, U.K.
J Am Chem Soc ; 143(10): 3934-3943, 2021 03 17.
Article em En | MEDLINE | ID: mdl-33660507
ABSTRACT
The nature of anionic alkali metals in solution is traditionally thought to be "gaslike" and unperturbed. In contrast to this noninteracting picture, we present experimental and computational data herein that support ion pairing in alkalide solutions. Concentration dependent ionic conductivity, dielectric spectroscopy, and neutron scattering results are consistent with the presence of superalkali-alkalide ion pairs in solution, whose stability and properties have been further investigated by DFT calculations. Our temperature dependent alkali metal NMR measurements reveal that the dynamics of the alkalide species is both reversible and thermally activated suggesting a complicated exchange process for the ion paired species. The results of this study go beyond a picture of alkalides being a "gaslike" anion in solution and highlight the significance of the interaction of the alkalide with its complex countercation (superalkali).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article