<?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>2026-05-30T04:37:57Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/39360" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/39360</identifier><datestamp>2026-02-03T11:31:55Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</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>Azuperylene: The Nonalternant Isomer of Perylene</dc:title>
   <dc:creator>Liu, Shengpei</dc:creator>
   <dc:creator>Díaz-Fernández, Marcos</dc:creator>
   <dc:creator>Zhang, Menglin</dc:creator>
   <dc:creator>Huang, Fei</dc:creator>
   <dc:creator>Chen, Yong</dc:creator>
   <dc:creator>Yang, Yudong</dc:creator>
   <dc:creator>Marín-Beloqui, José Manuel</dc:creator>
   <dc:creator>Lan, Jingbo</dc:creator>
   <dc:creator>You, Jingsong</dc:creator>
   <dc:creator>Casado-Cordón, Juan</dc:creator>
   <dc:creator>Zhang, Cheng</dc:creator>
   <dc:subject>Química física</dc:subject>
   <dc:subject>Electrónica órganica</dc:subject>
   <dcterms:abstract>The isoelectronic isomer of perylene, hereafter&#xd;
called as azuperylene, has been prepared. Electronic&#xd;
structure analysis reveals that the new isomer can be&#xd;
described as a union of two antiparallel azulenes in which&#xd;
the azulene-type aromatic character of the starting azulene&#xd;
is partially retained. Four 2,8-dialkoxy (i.e., ethoxy,&#xd;
n-butoxy, n-hexyloxy, and n-octyloxy) functionalized&#xd;
derivatives of the new isomer core have been prepared.&#xd;
The solid-state structures of the new compounds have&#xd;
been resolved showing exceptional herringbone π–π&#xd;
stacking ideal for charge transport. Organic field-effect&#xd;
transistors on sublimated substrates display an excellent&#xd;
hole transport mobility up to 1.03 cm2 V−1 s−1 that largely&#xd;
surpasses that of perylene and reveals the great potential&#xd;
for charge transport of this new class of nonbenzenoid&#xd;
compounds.</dcterms:abstract>
   <dcterms:dateAccepted>2025-07-16T10:01:35Z</dcterms:dateAccepted>
   <dcterms:available>2025-07-16T10:01:35Z</dcterms:available>
   <dcterms:created>2025-07-16T10:01:35Z</dcterms:created>
   <dcterms:issued>2025-05</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Liu, S., Díaz‐Fernández, M., Zhang, M., Huang, F., Chen, Y., Yang, Y., ... &amp; Zhang, C. (2025). Azuperylene: The Nonalternant Isomer of Perylene. Angewandte Chemie, e202505897.</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/39360</dc:identifier>
   <dc:identifier>10.1002/anie.202505897</dc:identifier>
   <dc:language>eng</dc:language>
   <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>
   <dc:publisher>Wiley</dc:publisher>
</qdc:qualifieddc>
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