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            <subfield code="a">Vasseur, G.</subfield>
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            <subfield code="a">p Band Dispersion Along Conjugated Organic Nanowires Synthesized on a Metal Oxide Semiconductor</subfield>
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            <subfield code="c">2016</subfield>
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            <subfield code="a">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.</subfield>
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            <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 635919-SURFINK</subfield>
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            <subfield code="a">Biochemistry</subfield>
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            <subfield code="a">Colloid and Surface Chemistry</subfield>
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            <subfield code="a">Chemistry (miscellaneous)</subfield>
            <subfield code="c">2016</subfield>
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            <subfield code="a">Abadia, M.</subfield>
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            <subfield code="a">Miccio, L.A.</subfield>
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            <subfield code="a">Brede, J.</subfield>
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            <subfield code="a">Garcia-Lekue, A.</subfield>
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            <subfield code="a">De Oteyza, D.G.</subfield>
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            <subfield code="a">Rogero, C.</subfield>
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            <subfield code="a">Lobo-Checa, J.</subfield>
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            <subfield code="a">Ortega, J.E.</subfield>
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            <subfield code="g">138, 17 (2016), 5685-5692</subfield>
            <subfield code="p">J. Am. Chem. Soc.</subfield>
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