<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-28T20:58:32Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/32632" metadataPrefix="dim">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/32632</identifier><datestamp>2025-03-26T19:10:04Z</datestamp><setSpec>com_10324_28542</setSpec><setSpec>com_10324_952</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_28543</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="536162ab0f92efec" confidence="500" orcid_id="0000-0003-4804-8751">Peñas de Frutos, Marconi Nicolás</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="c22040e8c139d9c1" confidence="500" orcid_id="0000-0002-8492-6825">Bartolomé Albistegui, María del Camino</dim:field>
<dim:field mdschema="dc" element="contributor" qualifier="author" authority="1340d9428d051fee" confidence="500" orcid_id="0000-0001-8649-239X">Espinet Rubio, Pablo</dim:field>
<dim:field mdschema="dc" element="date" qualifier="accessioned">2018-11-14T08:34:33Z</dim:field>
<dim:field mdschema="dc" element="date" qualifier="issued">2018</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="citation" lang="es">Organometallics, 2018, 37 (20), pp 3533–3542</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="issn" lang="es">0276-7333</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="uri">http://uvadoc.uva.es/handle/10324/32632</dim:field>
<dim:field mdschema="dc" element="identifier" qualifier="doi" lang="es">10.1021/acs.organomet.8b00227</dim:field>
<dim:field mdschema="dc" element="description" lang="es">Producción Científica</dim:field>
<dim:field mdschema="dc" element="description" qualifier="abstract" lang="es">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].</dim:field>
<dim:field mdschema="dc" element="description" qualifier="embargo" lang="es">2019-09-09</dim:field>
<dim:field mdschema="dc" element="description" qualifier="lift">2019-09-09</dim:field>
<dim:field mdschema="dc" element="description" qualifier="project" lang="es">Ministerio de Economía, Industria y Competitividad (Projects CTQ2016-80913-P, CTQ2014-52796-P, and CTQ2017-89217-P)</dim:field>
<dim:field mdschema="dc" element="description" qualifier="project" lang="es">Junta de Castilla y León (programa de apoyo a proyectos de investigación - Ref. VA051P17)</dim:field>
<dim:field mdschema="dc" element="format" qualifier="mimetype" lang="es">application/pdf</dim:field>
<dim:field mdschema="dc" element="language" qualifier="iso" lang="es">eng</dim:field>
<dim:field mdschema="dc" element="publisher" lang="es">American Chemical Society</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="accessRights" lang="es">info:eu-repo/semantics/openAccess</dim:field>
<dim:field mdschema="dc" element="rights" qualifier="holder" lang="es">© American Chemical Society</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es">Química organometálica</dim:field>
<dim:field mdschema="dc" element="subject" qualifier="classification" lang="es">Organometallic chemistry</dim:field>
<dim:field mdschema="dc" element="title" lang="es">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</dim:field>
<dim:field mdschema="dc" element="type" lang="es">info:eu-repo/semantics/article</dim:field>
<dim:field mdschema="dc" element="relation" qualifier="publisherversion" lang="es">https://pubs.acs.org/doi/10.1021/acs.organomet.8b00227</dim:field>
<dim:field mdschema="dc" element="peerreviewed" lang="es">SI</dim:field>
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