On-Surface Thermal Stability of a Graphenic Structure Incorporating a Tropone Moiety
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Rodríguez Márquez, Irene; Villalobos Romero, Federico; Cuerva Carvajal, Juan Manuel; González Campaña, AraceliEditorial
MDPI
Materia
On-surface synthesis Graphene nanoribbons Retro-Buchner reaction Intramolecular rearrangement Scanning tunneling microscope Non-contact atomic force microscope CO functionalized tip X-ray photoelectron spectroscopy
Date
2022-01-29Referencia bibliográfica
Márquez, I.R.; Ruíz del Árbol, N.; Urgel, J.I.; Villalobos, F.; Fasel, R.; López, M.F.; Cuerva, J.M.; Martín-Gago, J.A.; Campaña, A.G.; Sánchez-Sánchez, C. On-Surface Thermal Stability of a Graphenic Structure Incorporating a Tropone Moiety. Nanomaterials 2022, 12, 488. [https://doi.org/10.3390/nano12030488]
Sponsorship
Junta de Andalucía-Consejería de Economía y Conocimiento B-FQM-428-UGR20, BES-2015-072642, RYC2018-024364-I; MCIN; Ministerio de Universidades FPU18/05938; European Commission FOTOART-CM S2018/NMT-4367; European Research Council; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 200020-182015; European Social Fund; Universidad de Granada; European Regional Development Fund 011033, PID2020-113142RB-C21, S2018/NMT-4367; National Center of Competence in Research Materials’ Revolution: Computational Design and Discovery of Novel Materials 51NF40-182892; Agencia Estatal de InvestigaciónAbstract
On-surface synthesis, complementary to wet chemistry, has been demonstrated to be a
valid approach for the synthesis of tailored graphenic nanostructures with atomic precision. Among
the different existing strategies used to tune the optoelectronic and magnetic properties of these
nanostructures, the introduction of non-hexagonal rings inducing out-of-plane distortions is a promising pathway that has been scarcely explored on surfaces. Here, we demonstrate that non-hexagonal
rings, in the form of tropone (cycloheptatrienone) moieties, are thermally transformed into phenyl or
cyclopentadienone moieties upon an unprecedented surface-mediated retro–Buchner-type reaction
involving a decarbonylation or an intramolecular rearrangement of the CO unit, respectively.