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            <subfield code="a">10.1039/c6dt03010f</subfield>
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            <subfield code="a">Iturmendi, Amaia</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Dimethylphosphinate bridged binuclear Rh(i) catalysts for the alkoxycarbonylation of aromatic C-H bonds</subfield>
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            <subfield code="c">2016</subfield>
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            <subfield code="a">A variety of binuclear rhodium(I) complexes featuring two bridging dimethylphosphinate ligands ((CH3)2PO2-) have been prepared and tested in the alkoxycarbonylation of aromatic C–H bonds. The complex [Rh(µ-¿O,O'-(CH3)2PO2)(cod)]2 has been prepared by a reaction of [Rh(µ-MeO)(cod)]2 with 2 equivalents of dimethylphosphinic acid. Binuclear complexes [Rh(µ-¿O,O'-(CH3)2PO2)(CO)L]2 (L = PPh3, P(OMe)Ph2 and P(OPh)3) were obtained by carbonylation of the related mononuclear complexes [Rh(¿O-(CH3)2PO2)(cod)(L)], which were prepared in situ by the reaction of [Rh(µ-¿O,O'-(CH3)2PO2)(cod)]2 with 2 equivalents of L. Conversely, if L = IPr, the reaction of [Rh(µ-¿O,O'-(CH3)2PO2)(CO)L]2 with carbon monoxide affords the mononuclear complex [Rh(¿O-(CH3)2PO2)(CO)2IPr]. The subsequent reaction with trimethylamine N-oxide gives the corresponding binuclear complex [Rh(µ-¿O,O'-(CH3)2PO2)(CO)(IPr)]2 by abstraction of one of the carbonyl ligands. Complexes [Rh(µ-¿O,O'-(CH3)2PO2)(cod)]2 and [Rh(¿O-(CH3)2PO2)(cod)(L)] (L = IPr, PPh3, P(OMe)Ph2, P(OPh)3) are active precatalysts in the alkoxycarbonylation of C–H bonds, with the ligand system playing a key role in the catalytic activity. The complexes that feature more labile Rh–L bonds give rise to better catalysts, probably due to the more straightforward substitution of L by a second carbonyl ligand, since a more electrophilic carbonyl carbon atom is more susceptible toward aryl migration. In fact, complexes [Rh(µ-¿O,O'-(CH3)2PO2)(CO)2]2 and [Rh(µ-Cl)(CO)2]2, generated in situ from [Rh(µ-¿O,O'-(CH3)2PO2)(cod)]2 and [Rh(µ-Cl)(cod)2]2, respectively, are the most active catalysts tested in this work.</subfield>
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            <subfield code="a">All rights reserved</subfield>
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            <subfield code="a">Inorganic Chemistry</subfield>
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            <subfield code="0">(orcid)0000-0002-8220-6031</subfield>
            <subfield code="a">Sanz Miguel, Pablo J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Popoola, Saheed A.</subfield>
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            <subfield code="a">Al-Saadi, Abdulaziz A.</subfield>
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            <subfield code="a">Iglesias, Manuel</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0001-7154-7239</subfield>
            <subfield code="a">Oro, Luis A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">2010</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Química Inorgánica</subfield>
            <subfield code="c">Área Química Inorgánica</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
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            <subfield code="c">Proy. investigación HWA</subfield>
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            <subfield code="g">45, 42 (2016), 16955-16965</subfield>
            <subfield code="p">Dalton Trans.</subfield>
            <subfield code="t">Dalton Transactions</subfield>
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