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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 () and Thomas E. Albrecht-Schönzart ()
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Brian N. Long: Florida State University
María J. Beltrán-Leíva: Florida State University
Joseph M. Sperling: Florida State University
Todd N. Poe: Florida State University
Cristian Celis-Barros: Florida State University
Thomas E. Albrecht-Schönzart: Florida State University

Nature Communications, 2023, vol. 14, issue 1, 1-9

Abstract: 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.

Date: 2023
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DOI: 10.1038/s41467-023-39481-7

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