Room temperature crystal field splitting of curium resolved by circularly polarized luminescence spectroscopy


Coordination of Cm(III) with a chiral decadentate ligand N,N,N′,N′-tetrakis[(6-carboxypyridin-2-yl)methyl]-1,2-diaminocyclohexane (tpadac) generated complexes with strong luminescence allowing for the unprecedented measurement of well-resolved Cm(III) circularly polarized luminescence spectra. Quantitative resolution of the electronic structure of the [Cm(tpadac)][K] complexes was achieved at room temperature, highlighting the strength of the combination of luminescence and circularly polarized luminescence spectroscopies to unravel the fundamental electronic structure of Cm(III). These results are a clear demonstration that these spectroscopies are powerful yet simple tools for the fundamental understanding of electronic structure, which opens the door to future investigations of other Cm(III) complexes in geometries relevant to nuclear applications, and even other 5f-elements.

Graphical abstract: Room temperature crystal field splitting of curium resolved by circularly polarized luminescence spectroscopy



Source link

More From Author

Inverse opal anatase/rutile TiO2 multi-heterojunctions enable efficient photoelectrochemical water splitting

Ethanol-assisted synthesis of titanium-rich TS-1 zeolite: a new hexa-coordinated Ti site for efficient propylene epoxidation

Leave a Reply

Your email address will not be published. Required fields are marked *