锕系元素
镧系元素
多金属氧酸盐
化学
配位复合体
无机化学
金属
有机化学
催化作用
离子
作者
Ian Colliard,Gauthier J.‐P. Deblonde
出处
期刊:JACS Au
[American Chemical Society]
日期:2024-05-09
卷期号:4 (7): 2503-2513
被引量:3
标识
DOI:10.1021/jacsau.4c00245
摘要
Experimental studies involving actinide compounds are inherently limited in scope due to the radioactive nature of these elements and the scarcity and cost of their research isotopes. Now, ∼80 years after the introduction of the actinide concept by Glenn Seaborg, we still only have a limited understanding of the coordination chemistry of f-block metals when compared to more common elements such as the s-, p-, and d-blocks. This is particularly true for transplutonium actinides (Am, Cm, Bk, etc.) whose chemistry is often considered similar to trivalent lanthanides-mainly because of the lack of experimental data. We here report a metal-ligand system for which lanthanide and heavy actinide coordination compounds can be synthesized efficiently (i.e., requiring only a few micrograms) under identical conditions. Seventeen single crystal XRD structures of trivalent f-elements complexed to the polyoxometalate (POM) PW
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