<?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>2026-04-13T04:11:23Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/22854" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/22854</identifier><datestamp>2024-06-18T13:58:05Z</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>Novel NHC-Based Au(I) Complexes as Precursors of Highly Pure Au(0) Nuggets under Oxidative Conditions</dc:title>
   <dc:creator>Font Rubio, Pau</dc:creator>
   <dc:creator>Tzouras, Nikolaos V.</dc:creator>
   <dc:creator>Papastavrou, Argyro T.</dc:creator>
   <dc:creator>Vougioukalakis, Georgios C.</dc:creator>
   <dc:creator>Ribas Salamaña, Xavi</dc:creator>
   <dc:subject>Catàlisi</dc:subject>
   <dc:subject>Catalysis</dc:subject>
   <dc:subject>Catalitzadors</dc:subject>
   <dc:subject>Catalysts</dc:subject>
   <dc:subject>Reaccions d'addició</dc:subject>
   <dc:subject>Addition reactions</dc:subject>
   <dc:subject>Reaccions químiques</dc:subject>
   <dc:subject>Chemical reactions</dc:subject>
   <dcterms:abstract>The Lewis-acidic character and robustness of NHC-Au(I) complexes enable them to catalyze a large number of reactions, and they are enthroned as the catalysts of choice for many transformations among polyunsaturated substrates. More recently, Au(I)/Au(III) catalysis has been explored either by utilizing external oxidants or by seeking oxidative addition processes with catalysts featuring pendant coordinating groups. Herein, we describe the synthesis and characterization of N-heterocyclic carbene (NHC)-based Au(I) complexes, with and without pendant coordinating groups, and their reactivity in the presence of different oxidants. We demonstrate that when using iodosylbenzene-type oxidants, the NHC ligand undergoes oxidation to afford the corresponding NHC=O azolone products concomitantly with quantitative gold recovery in the form of Au(0) nuggets ~0.5 mm in size. The latter were characterized by SEM and EDX-SEM showing purities above 90%. This study shows that NHC-Au complexes can follow decomposition pathways under certain experimental conditions, thus challenging the believed robustness of the NHC-Au bond and providing a novel methodology to produce Au(0) nuggets</dcterms:abstract>
   <dcterms:abstract>The research project was supported by MINECO-Spain, PID2019-104498GB-I00 to X.R., as well as by the Hellenic Foundation for Research and Innovation (H.F.R.I.) under the “1st Call for H.F.R.I. Research Projects to support Faculty Members &amp; Researchers and the procurement of&#xd;
high-cost research equipment grant” (Project Number: 16)</dcterms:abstract>
   <dcterms:dateAccepted>2024-06-18T13:58:05Z</dcterms:dateAccepted>
   <dcterms:available>2024-06-18T13:58:05Z</dcterms:available>
   <dcterms:created>2024-06-18T13:58:05Z</dcterms:created>
   <dcterms:issued>2023-03-01</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/10256/22854</dc:identifier>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/molecules28052302</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1420-3049</dc:relation>
   <dc:relation>PID2019-104498GB-I00</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-104498GB-I00/ES/NANOCAPSULAS COMO PLATAFORMAS SUPRAMOLECULARES PARA LA FUNCIONALIZACION REGIOSELECTIVA DE FULLERENOS Y CATALISIS EN EL ESPACIO CONFINADO/</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>MDPI (Multidisciplinary Digital Publishing Institute)</dc:publisher>
   <dc:source>Molecules, 2023, vol. 28, núm. 5, p. 2302</dc:source>
   <dc:source>Articles publicats (D-Q)</dc:source>
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