<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-01T19:53:44Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/27458" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/27458</identifier><datestamp>2026-02-03T11:54:25Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Molecular Materials For Organic Electronics.</dc:title>
   <dc:creator>González Núñez, Raúl</dc:creator>
   <dc:creator>Martínez, Gabriel</dc:creator>
   <dc:creator>Ávila-Rovelo, Nelson Ricardo</dc:creator>
   <dc:creator>Ruiz-Carretero, Amparo</dc:creator>
   <dc:creator>Ponce-Ortiz, Rocío</dc:creator>
   <dc:subject>Electrónica órganica</dc:subject>
   <dc:subject>Semiconductores orgánicos</dc:subject>
   <dcterms:abstract>Organic materials have proven to be efficient active materials in electronics, being possible&#xd;
alternatives to inorganic semiconductors in electronic devices, such as organic field effects transistors&#xd;
(OFETs) or organic solar cells. The versatility of organic synthesis allows us to endow small molecules&#xd;
or polymers with the desired optoelectronic properties. However, the final efficiency of a given device&#xd;
is not only based on the molecular design but also on the way the molecules assemble. In this sense,&#xd;
non-covalent interactions play a crucial role as they are able to control the supramolecular assembly.&#xd;
Hydrogen-bonding has been proven a promising strategy to improve the film morphology in organic&#xd;
electronic devices with semiconductors able to efficiently transport charges. In this project, two&#xd;
compounds have been studied, based on a straightforward diketopyrrolopyrrole (DPP) with a&#xd;
thiophene-capped as the electroactive component and amide groups serving as the hydrogen-bonding&#xd;
units1. Theamide groups are positioned with two different topologies, C-centered (C-1) or N-centered&#xd;
(N-1) which are five carbons apart from the lactam rings of the DPP. We have compared these materials&#xd;
with the control derivative, 1, whose structure lack amide groups (Figure 1). Finally, the potential of&#xd;
these semicondcutors as active components in organic electronics have been tested in organic field&#xd;
effects transistors (OFETs).</dcterms:abstract>
   <dcterms:dateAccepted>2023-09-07T11:54:10Z</dcterms:dateAccepted>
   <dcterms:available>2023-09-07T11:54:10Z</dcterms:available>
   <dcterms:created>2023-09-07T11:54:10Z</dcterms:created>
   <dcterms:issued>2023</dcterms:issued>
   <dc:type>conference output</dc:type>
   <dc:identifier>https://hdl.handle.net/10630/27458</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>1st Stelorg Symposium On (Macro)Molecular Electronics and Spintronics</dc:relation>
   <dc:relation>Estrasburgo, Francia</dc:relation>
   <dc:relation>Agosto 2023</dc:relation>
   <dc:rights>open access</dc:rights>
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