2026-04-14T15:00:24Zhttps://uvadoc.uva.es/oai/request

oai:uvadoc.uva.es:10324/314622025-02-20T12:23:04Zcom_10324_1186com_10324_931com_10324_894com_10324_28542com_10324_952col_10324_1404col_10324_28543

Martín Ruiz, Blanca Pérez Ortega, Ignacio Albéniz Jiménez, Ana Carmen 2018-09-09T16:26:19Z 2018-09-09T16:26:19Z 2018 Organometallics, 2018, Vol. 37, p. 1074-1085 http://uvadoc.uva.es/handle/10324/31462 10.1021/acs.organomet.8b00065 A large variety of α-(pentafluorophenylmethyl)benzylic palladium complexes with different ligands have been synthesized and char- acterized. Multinuclear NMR spectroscopic data allow to determine the σ-or η3-benzylic nature of the complexes in solution. The adoption of either coordination mode is a function of the number of ligands coordinated to palladium and, remarkably, the presence of bulky phosphines favors the adoption of a bidentate η3-benzylic mode and palladium pentacoordinated complexes. Experimental data and DFT calculations indicate that this five- coordination could alleviate the steric hindrance of two cis bulky phosphines. The benzylic complexes show a rich fluxional behavior that involves both ligand exchange and σ- to η3-benzylic interconversion. eng info:eu-repo/semantics/openAccess Chemistry Organometallic Chemistry Benzylic Complexes of Palladium(II): Bonding modes and Penta- coordination for Steric Relief info:eu-repo/semantics/article