<?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>2026-04-28T19:07:06Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/31461" metadataPrefix="marc">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/31461</identifier><datestamp>2025-02-20T12:24:06Z</datestamp><setSpec>com_10324_28542</setSpec><setSpec>com_10324_952</setSpec><setSpec>com_10324_894</setSpec><setSpec>com_10324_1186</setSpec><setSpec>com_10324_931</setSpec><setSpec>col_10324_28543</setSpec><setSpec>col_10324_1404</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
<leader>00925njm 22002777a 4500</leader>
<datafield tag="042" ind1=" " ind2=" ">
<subfield code="a">dc</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Martín Ruiz, Blanca</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Pérez Ortega, Ignacio</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Albéniz Jiménez, Ana Carmen</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="260" ind1=" " ind2=" ">
<subfield code="c">2018</subfield>
</datafield>
<datafield tag="520" ind1=" " ind2=" ">
<subfield code="a">The adoption of a pseudoallylic (η3) form makes palladium benzylic derivatives a class of stabilized palladium alkyls that can undergo β-H elimination reactions in a more controlled way. α-&#xd;
(Pentafluorophenylmethyl)benzyl palladium complexes have been studied and they&#xd;
decompose by β-H elimination to give palladium hydrides that, depending on the auxil-&#xd;
iary ligands can: a) transmetalate to another palladium atom and, by reductive elimina- tion, give hydrogenated products; this process is favored for a combination of bridging ligands (i.e halogens) and low coordinating ligands. b) Be used as a hydride source and get trapped by a diene to give palladium allylic derivatives. The presence of carbon mon- oxide does not induce a β-H elimination reactions and only CO insertion into the Pd- benzyl bond to give acyl derivatives is observed.</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">Organometallics, 2018, vol. 37, p. 1665-1670</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">http://uvadoc.uva.es/handle/10324/31461</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">10.1021/acs.organomet.8b00066</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Chemistry</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Organometallic Chemistry</subfield>
</datafield>
<datafield tag="245" ind1="0" ind2="0">
<subfield code="a">α-Substituted Benzylic Complexes of Palladium(II) as Precursors of Palladium Hydrides</subfield>
</datafield>
</record></metadata></record></GetRecord></OAI-PMH>