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<dc:creator>Martín Ruiz, Blanca</dc:creator>
<dc:creator>Pérez Ortega, Ignacio</dc:creator>
<dc:creator>Albéniz Jiménez, Ana Carmen</dc:creator>
<dc:date>2018</dc:date>
<dc:description>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.</dc:description>
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<dc:identifier>http://uvadoc.uva.es/handle/10324/31461</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>American Chemical Society</dc:publisher>
<dc:subject>Chemistry</dc:subject>
<dc:subject>Organometallic Chemistry</dc:subject>
<dc:title>α-Substituted Benzylic Complexes of Palladium(II) as Precursors of Palladium Hydrides</dc:title>
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