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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1002/hlca.202100044</dc:identifier><dc:language>eng</dc:language><dc:creator>Wilkinson, Eden-Taylor</dc:creator><dc:creator>Viguri, Fernando</dc:creator><dc:creator>Rodríguez, Ricardo</dc:creator><dc:creator>López, José A.</dc:creator><dc:creator>García-Orduña, Pilar</dc:creator><dc:creator>Lahoz, Fernando J.</dc:creator><dc:creator>Lamata, Pilar</dc:creator><dc:creator>Carmona, Daniel</dc:creator><dc:title>Strained Ruthenium Complexes Bearing Tridentate Guanidine-Derived Ligands</dc:title><dc:identifier>ART-2021-125303</dc:identifier><dc:description>The dimer [{(η6-p-cymene)RuCl}2(μ-Cl)2] (cymene=MeC6H4iPr) reacts with N,N′-bis(p-tolyl)-N′′-(2-pyridinylmethyl)guanidine (H2L1) and N,N′-bis(p-tolyl)-N′′-(2-diphenylphosphanoethyl)guanidine (H2L2), in the presence of NaSbF6, giving rise to chlorido compounds of formula [(η6-p-cymene)RuCl(H2L)][SbF6] (H2L=H2L1 (1), H2L2 (2)) in which the guanidine ligand adopts a κ2 chelate coordination mode. The related ligand (S)-N,N′-bis(p-tolyl)-N′′-(1-isopropyl, 2-diphenylphosphano ethyl)guanidine (H2L3) affords mixtures of the corresponding chlorido compound [(η6-p-cymene)RuCl(H2L3)][SbF6] (3) together with the complexes [(η6-p-cymene)RuCl2(H3L3)][SbF6] (4) and [(η6-p-cymene)Ru(κ3N,N′,P-HL3)][SbF6] (10) which contain phosphano-guanidinium and phosphano-guanidinate ions acting as monodentate and tridentate ligand, respectively. Compounds 1, 2 and mixture of 3/4/10 react with AgSbF6 rendering the cationic aqua-complexes [(η6-p-cymene)Ru(H2L)(OH2)][SbF6]2 (H2L=H2L1 (5), H2L2 (6), H2L3 (7)). These aqua-complexes exhibit a temperature-dependent fluxional process in solution. Experimental NMR studies and DFT theoretical calculations on complex 6 suggest that the process involves the exchange between two rotamers around one of the C−N guanidine bonds. Treatment of 5–7 with NaHCO3 renders the complexes [(η6-p-cymene)Ru(κ3N,N′,N′′-HL1)][SbF6] (8) and [(η6-p-cymene)Ru(κ3N,N′,P-HL)][SbF6] (HL=HL2 (9), HL3 (10)), respectively, in which the HL ligand adopts a fac κ3 coordination mode. The new complexes have been characterized by analytical and spectroscopic means, including the determination of the crystal structures of the compounds 1, 2, 5, 9 and 10, by X-ray diffractometric methods.</dc:description><dc:date>2021</dc:date><dc:source>http://zaguan.unizar.es/record/112383</dc:source><dc:doi>10.1002/hlca.202100044</dc:doi><dc:identifier>http://zaguan.unizar.es/record/112383</dc:identifier><dc:identifier>oai:zaguan.unizar.es:112383</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/CTQ2017-83421-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/CTQ2018-095561-BI00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/RYC-2013-13800</dc:relation><dc:identifier.citation>HELVETICA CHIMICA ACTA 104, 6 (2021), e2100044 [17 pp.]</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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