<?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>2026-04-18T03:18:45Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/473367" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/473367</identifier><datestamp>2024-11-04T07:14:04Z</datestamp><setSpec>com_2072_98</setSpec><setSpec>col_2072_378192</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Dissimilar catalytic behavior of molecular or colloidal palladium systems with a new NHC ligand</dc:title>
   <dc:creator>Gómez-Villarraga, Fernando</dc:creator>
   <dc:creator>De Tovar Villanueva, Jonathan</dc:creator>
   <dc:creator>Guerrero, Miguel</dc:creator>
   <dc:creator>Nolis Fañanas, Pau</dc:creator>
   <dc:creator>Parella Coll, Teodor</dc:creator>
   <dc:creator>Lecante, Pierre</dc:creator>
   <dc:creator>Romero Fernández, Nuria</dc:creator>
   <dc:creator>Escriche Martínez, Lluís</dc:creator>
   <dc:creator>Bofill Arasa, Roger</dc:creator>
   <dc:creator>Ros i Badosa, Josep</dc:creator>
   <dc:creator>Sala Román, Xavier</dc:creator>
   <dc:creator>Philippot, Karine</dc:creator>
   <dc:creator>García-Antón, Jordi</dc:creator>
   <dc:description>In this work, we describe the synthesis of a new N-heterocyclic carbene (NHC) ligand, derived from a hybrid pyrazole-imidazolium scaffold, namely 1-[2-(3,5-dimethylpyrazol-1-yl)ethyl]-3-((S)-1-phenylethyl)-3H-imidazol-2-ylidene (L). This ligand has been used as a stabilizer for the organometallic synthesis of palladium(0) nanoparticles (Pd NPs). L presents a better stabilizing effect than its pre-carbenic HLCl counterpart, allowing the formation of isolated Pd NPs while HLCl yields aggregated ones. Additionally, molecular Pd(ii) coordination compounds of L and HLCl were synthesized and characterized to better understand the coordination modes of these ligands. Both molecular and colloidal Pd systems have been further tested in catalytic C-C coupling processes. Three different types of reactions have been observed depending on the catalytic system: (i) the Suzuki-Miyaura reaction takes place with Pd molecular complexes; (ii) a secondary reaction, the dehalogenation of the substrate, is always detected and (iii) the C-C homocoupling between two molecules of bromoarenes is observed with colloidal catalysts.</dc:description>
   <dc:date>2017</dc:date>
   <dc:type>Article</dc:type>
   <dc:identifier>https://ddd.uab.cat/record/288386</dc:identifier>
   <dc:identifier>urn:10.1039/c7dt02729j</dc:identifier>
   <dc:identifier>urn:oai:ddd.uab.cat:288386</dc:identifier>
   <dc:identifier>urn:pure_id:34343846</dc:identifier>
   <dc:identifier>urn:scopus_id:85029303292</dc:identifier>
   <dc:identifier>urn:recercauab:ARE-89766</dc:identifier>
   <dc:identifier>urn:wos_id:000410392800031</dc:identifier>
   <dc:identifier>urn:recercauab:ARE-86251</dc:identifier>
   <dc:identifier>urn:articleid:14779234v46n35p11768</dc:identifier>
   <dc:identifier>urn:oai:egreta.uab.cat:publications/1546837b-3a6d-4d81-a489-d512ad642e19</dc:identifier>
   <dc:identifier>http://hdl.handle.net/2072/473367</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Ministerio de Economía y Competitividad CTQ2015-64261-R</dc:relation>
   <dc:relation>Ministerio de Economía y Competitividad CTQ2015-64436-P</dc:relation>
   <dc:relation>Dalton transactions ; Vol. 46, Issue 35 (August 2017), p. 11768-11778</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original.</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher/>
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