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基于蔻的二维网络:通过苏曼烯前体的表面骨架重排构建

Coronene-Based 2D Networks by On-Surface Skeletal Rearrangement of Sumanene Precursors.

作者信息

Pérez-Elvira Elena, Barragán Ana, Gallardo Aurelio, Santos José, Martín-Fuentes Cristina, Lauwaet Koen, Gallego José M, Miranda Rodolfo, Sakurai Hidehiro, Urgel José I, Björk Jonas, Martín Nazario, Écija David

机构信息

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

Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense.

出版信息

Angew Chem Int Ed Engl. 2025 Jan 10;64(2):e202414583. doi: 10.1002/anie.202414583. Epub 2024 Oct 25.

Abstract

The design of novel low-dimensional carbon materials is at the forefront of modern chemistry. Recently, on-surface covalent synthesis has emerged as a powerful strategy to synthesize previously precluded compounds and polymers. Here, we report a scanning probe microscopy study, complemented by theoretical calculations, on the sequential skeletal rearrangement of sumanene-based precursors into a coronene-based organometallic network by stepwise intra- and inter-molecular reactions on Au(111). Interestingly, upon higher annealing, the formed organometallic networks evolve into two-dimensional coronene-based covalently linked patches through intermolecular homocoupling reactions. A new reaction mechanism is proposed based on the role of C-Au-C motifs to promote two stepwise carbon-carbon couplings to form cyclobutadiene bridges. Our results pave avenues for the conversion of molecular precursors on surfaces, affording the design of unexplored two-dimensional organometallic and covalent materials.

摘要

新型低维碳材料的设计处于现代化学的前沿。最近,表面共价合成已成为合成以前难以制备的化合物和聚合物的有力策略。在此,我们报告一项扫描探针显微镜研究,并辅以理论计算,该研究是关于基于苏曼烯的前体通过在Au(111)上的分子内和分子间逐步反应顺序骨架重排为基于蒄的有机金属网络。有趣的是,在更高温度退火时,形成的有机金属网络通过分子间均偶联反应演变成基于蒄的二维共价连接斑块。基于C-Au-C基序在促进两步碳-碳偶联以形成环丁二烯桥中的作用,提出了一种新的反应机制。我们的结果为表面分子前体的转化开辟了道路,为设计未探索的二维有机金属和共价材料提供了可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fc0/11720390/20124e6df899/ANIE-64-e202414583-g002.jpg

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