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<dc:title>Coordinatively Unsaturated [RhCp*Rf2] (Cp* = C5Me5; Rf = C6F3Cl2-3,5), General Precursor to Cp*-Diaryl and Cp*-Halo-Aryl RhIII Complexes. Observing and Testing the Effect of Cp* as Electronic Buffer</dc:title>
<dc:creator>Peñas de Frutos, Marconi Nicolás</dc:creator>
<dc:creator>Bartolomé Albistegui, María del Camino</dc:creator>
<dc:creator>Espinet Rubio, Pablo</dc:creator>
<dc:subject>Química organometálica</dc:subject>
<dc:subject>Organometallic chemistry</dc:subject>
<dc:description>Producción Científica</dc:description>
<dc:description>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].</dc:description>
<dc:description>2019-09-09</dc:description>
<dc:description>2019-09-09</dc:description>
<dc:description>Ministerio de Economía, Industria y Competitividad (Projects CTQ2016-80913-P, CTQ2014-52796-P, and CTQ2017-89217-P)</dc:description>
<dc:description>Junta de Castilla y León (programa de apoyo a proyectos de investigación - Ref. VA051P17)</dc:description>
<dc:date>2018-11-14T08:34:33Z</dc:date>
<dc:date>2018</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Organometallics, 2018, 37 (20), pp 3533–3542</dc:identifier>
<dc:identifier>0276-7333</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/32632</dc:identifier>
<dc:identifier>10.1021/acs.organomet.8b00227</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://pubs.acs.org/doi/10.1021/acs.organomet.8b00227</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>© American Chemical Society</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>American Chemical Society</dc:publisher>
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