Solid-State NMR Techniques for the Structural Characterization of Cyclic Aggregates Based on Borane-Phosphane Frustrated Lewis Pairs

Molecules. 2020 Mar 19;25(6):1400. doi: 10.3390/molecules25061400.

Abstract

Modern solid-state NMR techniques offer a wide range of opportunities for the structural characterization of frustrated Lewis pairs (FLPs), their aggregates, and the products of cooperative addition reactions at their two Lewis centers. This information is extremely valuable for materials that elude structural characterization by X-ray diffraction because of their nanocrystalline or amorphous character, (pseudo-)polymorphism, or other types of disordering phenomena inherent in the solid state. Aside from simple chemical shift measurements using single-pulse or cross-polarization/magic-angle spinning NMR detection techniques, the availability of advanced multidimensional and double-resonance NMR methods greatly deepened the informational content of these experiments. In particular, methods quantifying the magnetic dipole-dipole interaction strengths and indirect spin-spin interactions prove useful for the measurement of intermolecular association, connectivity, assessment of FLP-ligand distributions, and the stereochemistry of adducts. The present review illustrates several important solid-state NMR methods with some insightful applications to open questions in FLP chemistry, with a particular focus on supramolecular associates.

Keywords: Frustrated Lewis pairs; aggregation; dipolar spectroscopy; internuclear distance measurement; solid-state NMR.

Publication types

  • Review

MeSH terms

  • Boranes / chemistry*
  • Cycloaddition Reaction
  • Lewis Bases / chemistry
  • Nuclear Magnetic Resonance, Biomolecular
  • Phosphines / chemistry*

Substances

  • Boranes
  • Lewis Bases
  • Phosphines
  • phosphine