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镧系配位固体中准晶近似物的化学工程

Chemical engineering of quasicrystal approximants in lanthanide-based coordination solids.

作者信息

Voigt Laura, Kubus Mariusz, Pedersen Kasper S

机构信息

Department of Chemistry, Technical University of Denmark, Kemitorvet, Building 207, DK-2800 Kgs, Lyngby, Denmark.

出版信息

Nat Commun. 2020 Sep 17;11(1):4705. doi: 10.1038/s41467-020-18328-5.

Abstract

Tessellation of self-assembling molecular building blocks is a promising strategy to design metal-organic materials exhibiting geometrical frustration and ensuing frustrated physical properties. Appearing in two-dimensional quasiperiodic phases, tilings consisting of five-vertex nodes are regarded as approximants for quasicrystals. Unfortunately, these structural motifs are exceedingly rare due to the complications of acquiring five-fold coordination confined to the plane. Lanthanide ions display the sufficient coordinative plasticity, and large ionic radii, to allow their incorporation into irregular molecule-based arrays. We herein present the use of ytterbium(II) as a five-vertex node in a two-dimensional coordination solid, YbI(4,4'-bipyridine). The semi-regular Archimedean tessellation structure verges on quasicrystallinity and paves the way for lanthanide-based metal-organic materials with interesting photonic and magnetic properties.

摘要

自组装分子构建块的镶嵌是设计具有几何阻挫及由此产生的阻挫物理性质的金属有机材料的一种很有前景的策略。由五顶点节点组成的平铺图案出现在二维准周期相中,被视为准晶体的近似物。不幸的是,由于在平面内获得五重配位的复杂性,这些结构 motif 极其罕见。镧系离子表现出足够的配位可塑性和较大的离子半径,使其能够掺入不规则的分子基阵列中。我们在此展示了在二维配位固体 YbI(4,4'-联吡啶) 中使用镱 (II) 作为五顶点节点。半规则的阿基米德镶嵌结构接近准晶态,为具有有趣光子和磁性的镧系基金属有机材料铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c6/7498582/c5837095e227/41467_2020_18328_Fig1_HTML.jpg

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