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    <subfield code="a">10.1002/ejic.202100399</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">ART-2021-127067</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Galiana-Cameo M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-2043-4864</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Variation on the p-acceptor ligand within a Rhi-N-Heterocyclic carbene framework: divergent catalytic outcomes for phenylacetylene-methanol transformations</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
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    <subfield code="a">A series of neutral and cationic rhodium complexes bearing IPr {IPr=1, 3-bis-(2, 6-diisopropylphenyl)imidazolin-2-carbene} and p-acceptor ligands are reported. Cationic species [Rh(¿4-cod)(IPr)(NCCH3)]+ and [Rh(CO)(IPr)(L)2]+ (L=pyridine, CH3CN) were obtained by chlorido abstraction in suitable complexes, whereas the cod-CO derivative [Rh(¿4-cod)(IPr)(CO)]+ was formed by the carbonylation of [Rh(¿4-cod)(IPr)(NCCH3)]+. Alternatively, neutral derivatives of type RhCl(IPr)(L)2 {L=tBuNC or P(OMe)3} can be accessed from [Rh(µ-Cl)(¿2-coe)(IPr)]2. In addition, the mononuclear species Rh(CN)(¿4-cod)(IPr) was prepared by cyanide-chlorido anion exchange, which after carbonylation afforded the unusual trinuclear compound [Rh{1¿C, 2¿N-(CN)}(CO)(IPr)]3. Divergent catalytic outcomes in the phenylacetylene-methanol transformations have been observed. Thus, enol ethers, arisen from hydroalkoxylation of the alkyne, were obtained with neutral Rh-CO catalyst precursors whereas dienol ethers were formed with cationic catalysts. Variable amounts of alkyne dimerization, cyclotrimerization or polymerization products were obtained in the absence of a strong p-acceptor ligand on the catalyst. © 2021 The Authors. European Journal of Inorganic Chemistry published by Wiley-VCH GmbH</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/IJCI-2015-27029</subfield>
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    <subfield code="u">http://creativecommons.org/licenses/by-nc-nd/3.0/es/</subfield>
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    <subfield code="a">CHEMISTRY, INORGANIC &amp; NUCLEAR</subfield>
    <subfield code="b">23 / 46 = 0.5</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Inorganic Chemistry</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q2</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Passarelli V.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1735-6439</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Pérez-Torrente J.J.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-3327-0918</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Di Giuseppe A.</subfield>
    <subfield code="0">(orcid)0000-0002-3666-5800</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Castarlenas R.</subfield>
    <subfield code="0">(orcid)0000-0003-4460-8678</subfield>
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    <subfield code="1">2010</subfield>
    <subfield code="2">760</subfield>
    <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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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">2021, 29 (2021), 2947-2957</subfield>
    <subfield code="p">Eur. j. inorg. chem.</subfield>
    <subfield code="t">European Journal of Inorganic Chemistry</subfield>
    <subfield code="x">1434-1948</subfield>
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