Resumen: Surface-confined dehalogenation reactions are versatile bottom-up approaches for the synthesis of carbonbased nanostructures with predefined chemical properties. However, for devices generally requiring low-conductivity substrates, potential applications are so far severely hampered by the necessity of a metallic surface to catalyze the reactions. In this work we report the synthesis of ordered arrays of poly(p-phenylene) chains on the surface of semiconducting TiO2(110) via a dehalogenative homocoupling of 4, 4¿- dibromoterphenyl precursors. The supramolecular phase is clearly distinguished from the polymeric one using low-energy electron diffraction and scanning tunneling microscopy as the substrate temperature used for deposition is varied. X-ray photoelectron spectroscopy of C 1s and Br 3d core levels traces the temperature of the onset of dehalogenation to around 475 K. Moreover, angle-resolved photoemission spectroscopy and tightbinding calculations identify a highly dispersive band characteristic of a substantial overlap between the precursor''s p states along the polymer, considered as the fingerprint of a successful polymerization. Thus, these results establish the first spectroscopic evidence that atomically precise carbon-based nanostructures can readily be synthesized on top of a transition-metal oxide surface, opening the prospect for the bottom-up production of novel molecule-semiconductor devices. Idioma: Inglés DOI: 10.1021/jacs.6b02151 Año: 2016 Publicado en: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 138, 17 (2016), 5685-5692 ISSN: 0002-7863 Factor impacto JCR: 13.858 (2016) Categ. JCR: CHEMISTRY, MULTIDISCIPLINARY rank: 10 / 166 = 0.06 (2016) - Q1 - T1 Factor impacto SCIMAGO: 7.492 - Biochemistry (Q1) - Colloid and Surface Chemistry (Q1) - Chemistry (miscellaneous) (Q1) - Catalysis (Q1)