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oai:uvadoc.uva.es:10324/326322025-03-26T19:10:04Zcom_10324_28542com_10324_952com_10324_894col_10324_28543

Peñas de Frutos, Marconi Nicolás Bartolomé Albistegui, María del Camino Espinet Rubio, Pablo Producción Científica The pentacoordinated [RhCp*Rf2] (Rf = C6F3Cl2-3,5) and the octahedral (μ-Cl)2[RhCp*Rf]2, obtained by stoichiometric rearrangement with (μ-Cl)2[RhCp*Cl]2, are general precursors of [RhCp*RfXL] (X = Rf, Cl; L = ligand) complexes, which were studied by NMR (L dissociation and fluxional processes) and X-ray diffraction (structural effects affecting the Rh–Cp* distances) techniques. The Rh–Cp*centroid distances decrease markedly for identical L in the order [RhCp*Rf2L] > [RhCp*RfClL] > [RhCp*Cl2L] and are further influenced regularly within each family by the trans influence of L (longer distances for higher trans influence of L). The structural effects observed reveal a remarkable capability of Cp* to act as an electron-density buffer, which attenuates the Rh electron density variations induced by the substituents in front of Cp* by releasing toward Rh or polarizing toward Cp*, on demand, the electron density of the Rh–Cp* bonds. This buffer effect explains the easy L dissociation from [RhCp*Rf2L] and the accessibility to formally 16e pentacoordinated [RhCp*Rf2]. 2018-11-14 2018 info:eu-repo/semantics/article Organometallics, 2018, 37 (20), pp 3533–3542 0276-7333 http://uvadoc.uva.es/handle/10324/32632 10.1021/acs.organomet.8b00227 eng https://pubs.acs.org/doi/10.1021/acs.organomet.8b00227 info:eu-repo/semantics/openAccess © American Chemical Society American Chemical Society