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      <dc:title>Coronene-Based 2D Networks by On-Surface Skeletal Rearrangement of Sumanene Precursors</dc:title>
      <dc:creator>Pérez-Elvira, Elena</dc:creator>
      <dc:creator>Barragán, Ana</dc:creator>
      <dc:creator>Gallardo, Aurelio</dc:creator>
      <dc:creator>Santos Barahona, José Manuel</dc:creator>
      <dc:creator>Martín-Fuentes, Cristina</dc:creator>
      <dc:creator>Lauwaet, Koen</dc:creator>
      <dc:creator>Gallego, José M.</dc:creator>
      <dc:creator>Miranda, Rodolfo</dc:creator>
      <dc:creator>Sakurai, Hidehiro</dc:creator>
      <dc:creator>Urgel, José I.</dc:creator>
      <dc:creator>Björk, Jonas</dc:creator>
      <dc:creator>Martín León, Nazario</dc:creator>
      <dc:creator>Écija, David</dc:creator>
      <dc:description>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.</dc:description>
      <dc:date>2025-05-21T10:42:17Z</dc:date>
      <dc:date>2025-05-21T10:42:17Z</dc:date>
      <dc:date>2024</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Pérez‐Elvira, Elena, et al. «Coronene‐Based 2D Networks by On‐Surface Skeletal Rearrangement of Sumanene Precursors». Angewandte Chemie International Edition, vol. 64, n.o 2, enero de 2025, p. e202414583. https://doi.org/10.1002/anie.202414583.</dc:identifier>
      <dc:identifier>10.1002/anie.202414583</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/120320</dc:identifier>
      <dc:identifier>https://doi.org/10.1002/anie.202414583</dc:identifier>
      <dc:identifier>https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202414583</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108532GB-I00/ES/DISEÑO EN SUPERFICIES Y PROPIEDADES FISICO-QUIMICAS DE POLIMEROS PI-CONJUGADOS/</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-114653RB-I00/ES/SINTESIS "BOTTON-UP" DE NANOESTRUCTURAS DE CARBONO: APLICACIONES PARA LA ENERGIA/</dc:relation>
      <dc:relation>PID2022-136961NB-I00</dc:relation>
      <dc:relation>JP21H05233</dc:relation>
      <dc:relation>JP21H05233</dc:relation>
      <dc:relation>JP21H05233</dc:relation>
      <dc:relation>JP21H05233</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
      <dc:publisher>Wiley</dc:publisher>
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