4.6 Article

Ground and excited states analysis of alkali metal ethylenediamine and crown ether complexes

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 23, Issue 36, Pages 20298-20306

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cp02552j

Keywords

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Funding

  1. Auburn University (AU)
  2. Auburn University Hopper Cluster, Alabama Supercomputer Center
  3. National Energy Research Scientific Computing Center a DOE Office of Science User Facility
  4. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]
  5. Harry Merriwether Fellowship
  6. National Science Foundation [CHE1940456]

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High-level electronic structure calculations were conducted to investigate neutral lithium, sodium, and potassium complexes with ethylenediamine and crown ether molecules, revealing different electron orbital characteristics and shell models for each type of complex. The study found that despite the similar nature of electrides (metal crown ether sandwich aggregates) and expanded metals (metal ammonia aggregates), their electronic band structures are expected to differ significantly. Li(15-crown-5) was identified as the only complex adopting a shell model similar to that of metal ammonia complexes, positioning the metal in the center of the crown ether.
High-level electronic structure calculations are carried out to obtain optimized geometries and excitation energies of neutral lithium, sodium, and potassium complexes with two ethylenediamine and one or two crown ether molecules. Three different sizes of crowns are employed (12-crown-4, 15-crown-5, 18-crown-6). The ground state of all complexes contains an electron in an s-type orbital. For the mono-crown ether complexes, this orbital is the polarized valence s-orbital of the metal, but for the other systems this orbital is a peripheral diffuse orbital. The nature of the low-lying electronic states is found to be different for each of these species. Specifically, the metal ethylenediamine complexes follow the previously discovered shell model of metal ammonia complexes (1s, 1p, 1d, 2s, 1f), but both mono- and sandwich di-crown ether complexes bear a different shell model partially due to their lower (cylindrical) symmetry and the stabilization of the 2s-type orbital. Li(15-crown-5) is the only complex with the metal in the middle of the crown ether and adopts closely the shell model of metal ammonia complexes. Our findings suggest that the electronic band structure of electrides (metal crown ether sandwich aggregates) and expanded metals (metal ammonia aggregates) should be different despite the similar nature of these systems (bearing diffuse electrons around a metal complex).

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