Nature Communications (Jun 2023)

Altering the spectroscopy, electronic structure, and bonding of organometallic curium(III) upon coordination of 4,4′−bipyridine

  • Brian N. Long,
  • María J. Beltrán-Leíva,
  • Joseph M. Sperling,
  • Todd N. Poe,
  • Cristian Celis-Barros,
  • Thomas E. Albrecht-Schönzart

DOI
https://doi.org/10.1038/s41467-023-39481-7
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 9

Abstract

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Abstract Structural and electronic characterization of (Cp′3Cm)2(μ−4,4′−bpy) (Cp′ = trimethylsilylcyclopentadienyl, 4,4′−bpy = 4,4′−bipyridine) is reported and provides a rare example of curium−carbon bonding. Cp′3Cm displays unexpectedly low energy emission that is quenched upon coordination by 4,4′−bipyridine. Electronic structure calculations on Cp′3Cm and (Cp′3Cm)2(μ−4,4′−bpy) rule out significant differences in the emissive state, rendering 4,4′−bipyridine as the primary quenching agent. Comparisons of (Cp′3Cm)2(μ−4,4′−bpy) with its samarium and gadolinium analogues reveal atypical bonding patterns and electronic features that offer insights into bonding between carbon with f-block metal ions. Here we show the structural characterization of a curium−carbon bond, in addition to the unique electronic properties never before observed in a curium compound.