期刊
NATURE CHEMISTRY
卷 8, 期 8, 页码 797-802出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nchem.2520
关键词
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资金
- European FP7 TALISMAN project
- European Commission
- JRC ITU USERLAB programme
- University of Edinburgh, European Cooperation in Science and Technology action [CM1006]
- Engineering and Physical Sciences Research Council [EP/H004823/1, EP/M010554/1]
- EPSRC [EP/M010554/1, EP/H004823/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/H004823/1, EP/M010554/1] Funding Source: researchfish
Studies of transuranic organometallic complexes provide a particularly valuable insight into covalent contributions to the metal-ligand bonding, in which the subtle differences between the transuranium actinide ions and their lighter lanthanide counterparts are of fundamental importance for the effective remediation of nuclear waste. Unlike the organometallic chemistry of uranium, which has focused strongly on U-III and has seen some spectacular advances, that of the transuranics is significantly technically more challenging and has remained dormant. In the case of neptunium, it is limited mainly to Np-IV. Here we report the synthesis of three new Np-III organometallic compounds and the characterization of their molecular and electronic structures. These studies suggest that Np-III complexes could act as single-molecule magnets, and that the lower oxidation state of Np-II is chemically accessible. In comparison with lanthanide analogues, significant d- and f-electron contributions to key Np-III orbitals are observed, which shows that fundamental neptunium organometallic chemistry can provide new insights into the behaviour of f-elements.
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