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Martín Ruiz, Blanca Pérez Ortega, Ignacio Albéniz Jiménez, Ana Carmen 2018-09-09T16:22:01Z 2018-09-09T16:22:01Z 2018 Organometallics, 2018, vol. 37, p. 1665-1670 http://uvadoc.uva.es/handle/10324/31461 10.1021/acs.organomet.8b00066 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- (Pentafluorophenylmethyl)benzyl palladium complexes have been studied and they decompose by β-H elimination to give palladium hydrides that, depending on the auxil- 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. MINECO (SGPI, grant CTQ2016-80913-P) application/pdf eng American Chemical Society info:eu-repo/semantics/openAccess Chemistry Organometallic Chemistry Palladium Benzyl complexes Hydrides Transmetalation α-Substituted Benzylic Complexes of Palladium(II) as Precursors of Palladium Hydrides info:eu-repo/semantics/article https://pubs.acs.org/doi/10.1021/acs.organomet.8b00066 SI