<?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>2026-04-18T06:01:56Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/464345" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/464345</identifier><datestamp>2024-11-04T04:39:21Z</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>15-Membered triolefinic macrocycles, their coordination chemistry with transition metals, and the catalytic properties of their palladium metal complexes : A review</dc:title>
   <dc:creator>Moreno-Mañas, Marcial</dc:creator>
   <dc:creator>Pleixats i Rovira, Roser</dc:creator>
   <dc:creator>Roglans, Anna</dc:creator>
   <dc:creator>Sebastián Pérez, Rosa Maria</dc:creator>
   <dc:creator>Vallribera Massó, Adelina</dc:creator>
   <dc:subject>Alkene ligands</dc:subject>
   <dc:subject>Macrocycles</dc:subject>
   <dc:subject>Heterocycles</dc:subject>
   <dc:subject>Olefin complexes</dc:subject>
   <dc:subject>Catalysis</dc:subject>
   <dc:description>(E,E,E)-1,6,11-Tris(arenesulfonyl)-1,6,11-triazacyclopentadeca-3,8,11-trienes, 1, are prepared from arenesulfonamides and trans-1,4-dibromo-2-butene. Macrocycles 1 coordinate palladium(0), platinum(0), and silver(I), and the palladium complexes are useful and reutilizable catalysts or precatalysts in Suzuki cross-couplings, butadiene telomerizations, hydroarylation of alkynes, and in the Heck reaction. Structurally related macrocycles are also available by similar synthetic procedures.</dc:description>
   <dc:date>2004</dc:date>
   <dc:type>Article</dc:type>
   <dc:identifier>https://ddd.uab.cat/record/268572</dc:identifier>
   <dc:identifier>urn:10.3998/ark.5550190.0005.414</dc:identifier>
   <dc:identifier>urn:oai:ddd.uab.cat:268572</dc:identifier>
   <dc:identifier>urn:articleid:15517012v2004n4p109</dc:identifier>
   <dc:identifier>urn:oai:egreta.uab.cat:publications/b9c3cb14-4b31-4077-86c1-9e37ae3c91ff</dc:identifier>
   <dc:identifier>urn:scopus_id:2942607092</dc:identifier>
   <dc:identifier>http://hdl.handle.net/2072/464345</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Arkivoc ; Vol. 2004, Issue 4 (2004), p. 109-129</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, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:format>application/pdf</dc:format>
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