Suppr超能文献

石墨烯/Ir(111)上的镝导向金属超分子网络

Dysprosium-directed metallosupramolecular network on graphene/Ir(111).

作者信息

Moreno Daniel, Cirera Borja, Parreiras Sofia O, Urgel José I, Giménez-Agulló Nelson, Lauwaet Koen, Gallego José M, Galán-Mascarós José R, Martínez José I, Ballester Pablo, Miranda Rodolfo, Écija David

机构信息

IMDEA Nanoscience, C/Faraday 9, Campus de Cantoblanco, 28049 Madrid, Spain.

出版信息

Chem Commun (Camb). 2021 Feb 7;57(11):1380-1383. doi: 10.1039/d0cc07315f. Epub 2021 Jan 12.

Abstract

The interest in exploiting the unique properties of lanthanides has led to the recent design of two-dimensional coordination networks incorporating f-block elements on metallic surfaces. In order to take this field to the next step of progression, it is necessary to electronically decouple these two-dimensional architectures from the metallic surface underneath. As a first step in this direction, we report the formation of dysprosium-directed metal-organic networks employing three-fold ligands as molecular linkers equipped with terminal carbonitrile functional groups on weakly interacting substrates such as Au(111) and graphene/Ir(111). We observe on both substrates identical quasi-hexagonal Dy-carbonitrile coordination networks based on majority five-fold nodes. Our findings provide perspectives for the formation of lanthanide coordination networks on graphene and related sp materials grown on metals.

摘要

对利用镧系元素独特性质的兴趣促使人们最近设计出在金属表面包含f族元素的二维配位网络。为了使该领域迈向进一步发展的阶段,有必要将这些二维结构与下方的金属表面进行电子解耦。作为朝这个方向迈出的第一步,我们报告了在诸如Au(111)和石墨烯/Ir(111)等弱相互作用基底上,使用具有末端腈官能团的三齿配体作为分子连接体形成镝导向的金属有机网络。我们在两种基底上都观察到基于多数五配位节点的相同准六边形Dy-腈配位网络。我们的发现为在金属上生长的石墨烯及相关sp材料上形成镧系配位网络提供了前景。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验