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通过解偶联的硼氮杂环的金属配位作用在金属基底上形成 BN 图案。

BN-Patterning of Metallic Substrates through Metal Coordination of Decoupled Borazines.

机构信息

Physics Department, Technical University of Munich, 85748, Garching, Germany.

School of Chemistry, Cardiff University, Park Place Main Building, Cardiff, CF10 3AT, United Kingdom.

出版信息

Chemistry. 2018 Jul 5;24(38):9565-9571. doi: 10.1002/chem.201800849. Epub 2018 Jun 20.

Abstract

We report on the synthesis of pyridine-terminated borazine derivatives, their molecular self-assembly as well as the electronic properties investigated on silver and copper surfaces by means of scanning tunneling microscopy and X-ray photoelectron spectroscopy. The introduction of pyridine functionalities allows us to achieve distinct supramolecular architectures with control of the interdigitation of the molecules by surface templating. On silver surfaces, the borazine derivatives arrange in a dense-packed hexagonal structure through van der Waals and H-bonding interactions, whereas on Cu(111), the molecules undergo metal coordination. The porosity and coordination symmetry of the reticulated structure depends on the stoichiometric ratio between copper adatoms and the borazine ligands, permitting an unusual three-fold coordinated Cu-pyridyl network. Finally, spectroscopy measurements indicate that the borazine core is electronically decoupled from the metallic substrate. We thus demonstrate that BNC-containing molecular units can be integrated into stable metal-coordination architectures on surfaces, opening pathways to patterned, BN-doped sheets with specific functionalities, for example, regarding the adsorption of polar guest gases.

摘要

我们报告了吡啶端基硼氮烷衍生物的合成、分子自组装以及通过扫描隧道显微镜和 X 射线光电子能谱在银和铜表面上研究的电子性质。吡啶官能团的引入允许我们通过表面模板控制分子的互穿插来实现不同的超分子结构。在银表面上,硼氮烷衍生物通过范德华力和氢键相互作用排列成密集的六方结构,而在 Cu(111)上,分子经历金属配位。网状结构的多孔性和配位对称性取决于铜原子和硼氮烷配体之间的化学计量比,允许出现不寻常的三配位 Cu-吡啶络合物网络。最后,光谱测量表明硼氮烷核与金属基底在电子上是解耦的。因此,我们证明了含 BNC 的分子单元可以整合到表面上稳定的金属配位结构中,为具有特定功能的图案化、掺硼氮的薄片开辟了途径,例如关于极性客体气体的吸附。

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