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Polymerization of well-aligned organic nanowires on unconventional substrates

AuthorsAbadia, Mikel; García-Lekue, Aran; Piquero-Zulaica, Ignacio; Lobo-Checa, Jorge ; Ortega, J. Enrique ; Brede, Jens; Rogero, Celia
Issue Date2018
Citation2nd ELECMI International Workshop (2018)
AbstractIn the early 1900's Fritz Ullmann first reported the synthesis of biaryls from aryl halides mediated by a fine copper powder, demonstrating with this the aromatic nucleophilic substitution mediated by copper, now known as Ullmann condensation reaction. More than hundred years after, this reaction is routinely used in numerous industrial applications and, nowadays it becomes widely used for the synthesis on metal surfaces of atomically precise graphene nanoribbons. The next step to move toward device applications requires performing the synthesis directly on suitable substrates such as semiconducting, insulating or magnetic substrates. Whit in this context, in the present work we explore the Ullmann based synthesis of polymers on magnetic and insulating substrates. In particular we demonstrate the aryl homocoupling synthesis of 4,4-Dibromo (or diiodo)-p-terphenyl precursor into molecular poly-p-phenylene wires on the semiconductor TiO2 surface and on the bimetallic (and ferromagnetic) GdAu2 surface alloy. Moreover, we propose a reaction pathway during the polymerization. To monitor the chemical reaction complementary microscopic and spectroscopic surface science techniques (scanning tunneling microscopy, X-ray photoemission spectroscopy, angle-resolved Photoemission spectroscopy) are used.
DescriptionResumen del trabajo presentado al 2nd ELECMI International Workshop celebrado en Zaragoza (España) del 11 al 13 de junio de 2018.
Appears in Collections:(CFM) Comunicaciones congresos
(ICV) Comunicaciones congresos
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