<?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>2026-04-17T22:52:42Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/19688" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/19688</identifier><datestamp>2024-06-18T13:56:32Z</datestamp><setSpec>com_2072_452955</setSpec><setSpec>com_2072_2054</setSpec><setSpec>col_2072_453073</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" 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>Double-Carrousel Mechanism for Mn-Catalyzed Dehydrogenative Amide Synthesis from Alcohols and Amines</dc:title>
   <dc:creator>Luque Urrutia, Jesús Antonio</dc:creator>
   <dc:creator>Pèlachs, Tània</dc:creator>
   <dc:creator>Solà i Puig, Miquel</dc:creator>
   <dc:creator>Poater Teixidor, Albert</dc:creator>
   <dc:subject>Amides -- Síntesi</dc:subject>
   <dc:subject>Amides -- Synthesis</dc:subject>
   <dc:subject>Catalitzadors</dc:subject>
   <dc:subject>Catalysts</dc:subject>
   <dcterms:abstract>We study with density functional theory calculations the mechanism of the original example of a base-metal-catalyzed synthesis of amides from alcohols and amines. A preliminary proposal of the mechanism of this reaction was experimentally reported by Milstein and co-workers. Instead of the proposed reaction mechanism with a hemilabile pincer amine arm, our DFT calculations describe a facile protocol, where the catalyst only produces aldehydes from alcohols. Once formaldehyde is formed from methanol, it reacts with the amine to form a second alcohol. This new alcohol undergoes the same procedure as methanol and creates the desired amide through a double-carrousel mechanism. The rate-determining step in the catalytic aldehyde synthesis corresponds to the H2 formation. However, in the nonmetal-catalyzed part of the mechanism, the interaction of formaldehyde with the amine is also quite kinetically demanding</dcterms:abstract>
   <dcterms:abstract>J.A.L.-U. thanks Universitat de Girona for an IFUdG2017 Ph.D.&#xd;
fellowship. A.P. is a Serra Húnter Fellow. A.P. and M.S. thank the&#xd;
Ministerio de Economía y Competitividad (MINECO) of Spain for&#xd;
projects PGC2018-097722-B-I00 and CTQ2017-85341-P;&#xd;
Generalitat de Catalunya for project 2017SGR39 and ICREA&#xd;
Academia prize 2019 to A.P.</dcterms:abstract>
   <dcterms:dateAccepted>2024-06-18T13:56:32Z</dcterms:dateAccepted>
   <dcterms:available>2024-06-18T13:56:32Z</dcterms:available>
   <dcterms:created>2024-06-18T13:56:32Z</dcterms:created>
   <dcterms:issued>info:eu-repo/date/embargoEnd/2022-05-06</dcterms:issued>
   <dcterms:issued>2021-05-06</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:type>peer-reviewed</dc:type>
   <dc:identifier>http://hdl.handle.net/10256/19688</dc:identifier>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acscatal.1c00693</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/2155-5435</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-097722-B-I00/ES/REDESCUBRIMIENTO IN SILICO DE MECANISMOS ASISTIDOS DUALES DE LA CATALISIS MONOMETALICA: HACIA EL TRABAJO EN CONDICIONES SUAVES/</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-85341-P/ES/AVANCES EN LA REACTIVIDAD DE FULLERENOS Y NANOTUBOS: ESTUDIOS TEORICO-EXPERIMENTALES DE CICLACIONES CATALIZADAS POR METALES DE TRANSICION/</dc:relation>
   <dc:rights>Reconeixement 4.0 Internacional</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Chemical Society</dc:publisher>
   <dc:source>ACS Catalysis, 2021, vol.11, núm. 10, p. 6155-6161</dc:source>
   <dc:source>Articles publicats (D-Q)</dc:source>
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