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      <dc:title>Electronic Properties of Naphthalimide-based Ladder-type Systems</dc:title>
      <dc:creator>González-Núñez, Raúl</dc:creator>
      <dc:creator>Alonso-Navarro, Matías J.</dc:creator>
      <dc:creator>Harbuzaru, Alexandra</dc:creator>
      <dc:creator>Segura, José L.</dc:creator>
      <dc:creator>Ponce-Ortiz, Rocío</dc:creator>
      <dc:subject>Semiconductores orgánicos</dc:subject>
      <dc:description>The tuneable electronic and structural properties of organic semiconductors together with their flexibility, &#xd;
light weight, high solution processing and low costs in comparison with inorganic semiconductors are &#xd;
some of the key points for the current interest in the development of π-conjugated small molecules and &#xd;
polymers for a variety of applications. In this project, a combined experimental and theoretical study of &#xd;
two ladder-type compounds functionalized with naphthalimides1&#xd;
(Figure 1) is performed with the aim to &#xd;
explore the impact of the structure on the optical and charge-transport properties. Compound &#xd;
NDI-TP-Ph-TP has an imidazole group as a spacer ring and NIP-TP-Ph-TP has a spacer ring of &#xd;
pyrazine type. The two molecular systems have been implemented in organic field effect transistors2&#xd;
(OFETs), to assess their potential as active materials in organic electronics. Both compounds show p-type mobility, moreover, NDI-TP-Ph-TP material also displays low n-type mobility, presenting a certain &#xd;
ambipolar character.</dc:description>
      <dc:date>2023-02-03T11:23:25Z</dc:date>
      <dc:date>2023-02-03T11:23:25Z</dc:date>
      <dc:date>2023-01-27</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/25894</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>Computing pi-conjugated compounds</dc:relation>
      <dc:relation>Madrid</dc:relation>
      <dc:relation>27/01/2023</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 Internacional</dc:rights>
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