<?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>2026-05-05T21:31:36Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/48998" metadataPrefix="ese">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/48998</identifier><datestamp>2022-07-18T09:32:59Z</datestamp><setSpec>com_10324_1186</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1404</setSpec></header><metadata><europeana:record xmlns:europeana="http://www.europeana.eu/schemas/ese/" xmlns:confman="org.dspace.core.ConfigurationManager" xmlns:doc="http://www.lyncode.com/xoai" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.europeana.eu/schemas/ese/ http://www.europeana.eu/schemas/ese/ESE-V3.4.xsd">
<dc:title>How aromatic fluorination exchanges the interaction role of pyridine with carbonyl compounds: The formaldehyde adduct</dc:title>
<dc:creator>López Alonso, Juan Carlos</dc:creator>
<dc:creator>Macario Farto, Alberto</dc:creator>
<dc:creator>Maris, Assimo</dc:creator>
<dc:creator>Alkorta, Ibon</dc:creator>
<dc:creator>Blanco Rodríguez, Susana</dc:creator>
<dc:subject>Aromatic fluorination</dc:subject>
<dc:subject>Pyridine</dc:subject>
<dc:subject>Carbonyl compounds</dc:subject>
<dc:subject>Pentafluoropyridine</dc:subject>
<dc:subject>Formaldehyde</dc:subject>
<dc:subject>23 Química</dc:subject>
<dc:description>Producción Científica</dc:description>
<dc:description>The rotational spectrum of the weakly bound complex&#xd;
pentafluoropyridineꞏꞏꞏformaldehyde has been investigated using&#xd;
Fourier transform microwave spectroscopy. From the analysis of the&#xd;
rotational parameters of the parent species and of the 13C and 15N&#xd;
isotopologues, the structural arrangement of the adduct has been&#xd;
unambiguously established. The full ring fluorination of pyridine has a&#xd;
dramatic effect on its binding properties: It alters the electron density&#xd;
distribution at the π-cloud of pyridine creating a π-hole and changing&#xd;
its electron donor-acceptor capabilities. In the complex, formaldehyde&#xd;
lies above the aromatic ring with one of the oxygen lone pairs, as&#xd;
conventionally envisaged, pointing toward its centre. This lone&#xd;
pairꞏꞏꞏπ-hole interaction, reinforced by a weak C-HꞏꞏꞏN interaction,&#xd;
indicates an exchange of the electron-acceptor roles of both&#xd;
molecules when compared to the pyridineꞏꞏꞏformaldehyde adduct.&#xd;
Tunnelling doublets due to the internal rotation of formaldehyde have&#xd;
also been observed and analysed leading to a discussion on the&#xd;
competition between lone pairꞏꞏꞏπ-hole and π ꞏꞏꞏπ staking interactions.</dc:description>
<dc:description>Ministerio de Economía y Competitividad (grant CTQ2016-75253-P)</dc:description>
<dc:description>Ministerio de Ciencia, Innovación y Universidades de España (project PGC2018-094644-B-C22)</dc:description>
<dc:description>Comunidad Autónoma de Madrid (grant P2018 / EMT-4329 AIRTEC-CM)</dc:description>
<dc:date>2021-10-11T09:30:24Z</dc:date>
<dc:date>2021-10-11T09:30:24Z</dc:date>
<dc:date>2021</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:identifier>Chemistry – A European Journal, 2021, vol.  27, n. 55,  p.13870 –13878</dc:identifier>
<dc:identifier>0947-6539</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/48998</dc:identifier>
<dc:identifier>10.1002/chem.202102163</dc:identifier>
<dc:identifier>13870</dc:identifier>
<dc:identifier>55</dc:identifier>
<dc:identifier>13878</dc:identifier>
<dc:identifier>Chemistry – A European Journal</dc:identifier>
<dc:identifier>27</dc:identifier>
<dc:identifier>1521-3765</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202102163</dc:relation>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© 2021 The Authors</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Wiley</dc:publisher>
<europeana:object>https://uvadoc.uva.es/bitstream/10324/48998/4/How-aromatic-fluorination-exchanges.pdf.jpg</europeana:object>
<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</europeana:rights>
<europeana:dataProvider>UVaDOC. Repositorio Documental de la Universidad de Valladolid</europeana:dataProvider>
<europeana:isShownAt>https://uvadoc.uva.es/handle/10324/48998</europeana:isShownAt>
</europeana:record></metadata></record></GetRecord></OAI-PMH>