<?xml version="1.0" encoding="UTF-8"?>
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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:10.1039/d0dt02713h</dc:identifier><dc:language>eng</dc:language><dc:creator>Parker, A.</dc:creator><dc:creator>Lamata, P.</dc:creator><dc:creator>Viguri, F.</dc:creator><dc:creator>Rodríguez, R.</dc:creator><dc:creator>López, J.A.</dc:creator><dc:creator>Lahoz, F.J.</dc:creator><dc:creator>García-Orduña, P.</dc:creator><dc:creator>Carmona, D.</dc:creator><dc:title>Half-sandwich complexes of osmium containing guanidine-derived ligands</dc:title><dc:identifier>ART-2020-120565</dc:identifier><dc:description>Pyridinyl- and phosphano-guanidino complexes of formula [(¿6-p-cymene)OsCl(H2L)][SbF6] (cymene = MeC6H4iPr; H2L = N, N'-bis(p-Tolyl)-N''-(2-pyridinylmethyl)guanidine, H2L1 (1) and N, N'-bis(p-Tolyl)-N''-(2-diphenylphosphanoethyl)guanidine, H2L2 (2)) have been prepared from the dimer [{(¿6-p-cymene)OsCl}2(µ-Cl)2] and H2L in the presence of NaSbF6. Treatment of complex 2 with HCl renders the phosphano-guanidinium complex [(¿6-p-cymene)OsCl2(H3L2)][SbF6] (3). Compounds 1 and 2 react with AgSbF6 rendering the cationic aqua complexes [(¿6-p-cymene)Os(H2L)(OH2)][SbF6]2 (H2L = H2L1 (4), H2L2 (5)). Addition of monodentate ligands L to compound 4 affords complexes of formula [(¿6-p-cymene)Os(H2L1)L][SbF6]2 (L = py (6), 4-(NHMe)py (7), CO (8), P(OMe)3 (9)). Treatment of complexes 4 and 5 with NaHCO3 renders the monocationic complexes [(¿6-p-cymene)Os(¿3N, N', N''-HL1)][SbF6] (10) and [(¿6-p-cymene)Os(¿3N, N', P-HL2)][SbF6] (11), respectively, in which the HL ligand adopts a fac-¿3 coordination mode. The new complexes have been characterised by analytical and spectroscopic means, including the determination of the crystal structures of the compounds 1-4, 6, 8, and 11, by X-ray diffractometric methods. The phosphano-guanidino complexes 2 and 5 exhibit a temperature dependent fluxional process in solution. The new 18 electron complexes 1, 2, 6, and 8-10 are active catalysts for the Friedel-Crafts reaction between trans-ß-nitrostyrene and N-methyl-2-methylindole. Conversions greater than 90% were obtained. Proton NMR studies support a mechanism involving the Brønsted-acid activation of trans-ß-nitrostyrene through the NH functionalities of the coordinated guanidine ligands.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/131298</dc:source><dc:doi>10.1039/d0dt02713h</dc:doi><dc:identifier>http://zaguan.unizar.es/record/131298</dc:identifier><dc:identifier>oai:zaguan.unizar.es:131298</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>Dalton Transactions 49, 39 (2020), 13601-13617</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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