Rheinfrank Erik, Pörtner Mathias, Nuñez Beyerle Maria Del Carmen, Haag Felix, Deimel Peter S, Allegretti Francesco, Seufert Knud, Barth Johannes V, Bocquet Marie-Laure, Feulner Peter, Auwärter Willi
Physics Department E20, Technical University of Munich, D-85748 Garching, Germany.
PASTEUR, Départment de Chimie, Ecole Normale Supérieure, PSL University, Sorbonne Université, CNRS, F-75005 Paris, France.
J Am Chem Soc. 2021 Sep 15;143(36):14581-14591. doi: 10.1021/jacs.1c04982. Epub 2021 Sep 3.
Actinide-based metal-organic complexes and coordination architectures encompass intriguing properties and functionalities but are still largely unexplored on surfaces. We introduce the in situ synthesis of actinide tetrapyrrole complexes under ultrahigh-vacuum conditions, on both a metallic support and a 2D material. Specifically, exposure of a tetraphenylporphyrin (TPP) multilayer to an elemental beam of thorium followed by a temperature-programmed reaction and desorption of surplus molecules yields bis(porphyrinato)thorium (Th(TPP)) assemblies on Ag(111) and hexagonal boron nitride/Cu(111). A multimethod characterization including X-ray photoelectron spectroscopy, scanning tunneling microscopy, temperature-programmed desorption, and complementary density functional theory modeling provides insights into conformational and electronic properties. Supramolecular assemblies of Th(TPP) as well as individual double-deckers are addressed with submolecular precision, e.g., demonstrating the reversible rotation of the top porphyrin in Th(TPP) by molecular manipulation. Our findings thus demonstrate prospects for actinide-based functional nanoarchitectures.
基于锕系元素的金属有机配合物和配位结构具有引人入胜的性质和功能,但在表面上仍 largely 未被探索。我们介绍了在超高真空条件下,在金属载体和二维材料上原位合成锕系四吡咯配合物。具体而言,将四苯基卟啉(TPP)多层膜暴露于钍元素束,随后进行程序升温反应并解吸多余分子,在 Ag(111) 和六方氮化硼/Cu(111) 上生成双(卟啉基)钍(Th(TPP))组装体。包括 X 射线光电子能谱、扫描隧道显微镜、程序升温脱附和互补密度泛函理论建模在内的多方法表征提供了对构象和电子性质的见解。Th(TPP) 的超分子组装体以及单个双层结构以亚分子精度进行研究,例如通过分子操纵证明 Th(TPP) 中顶部卟啉的可逆旋转。因此,我们的发现展示了基于锕系元素的功能纳米结构的前景。