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    <subfield code="a">Batuecas, María</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1430-1440</subfield>
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    <subfield code="a">Recent advances on the chemistry of transition metal complexes with monoanionic bidentate silyl ligands</subfield>
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    <subfield code="c">2024</subfield>
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    <subfield code="a">The chemistry of transition-metal (TM) complexes with monoanionic bidentate (κ2-L,Si) silyl ligands has considerably grown in recent years. This work summarizes the advances in the chemistry of TM-(κ2-L,Si) complexes (L=N-heterocycle, phosphine, N-heterocyclic carbene, thioether, ester, silylether or tetrylene). The most common synthetic method has been the oxidative addition of the Si−H bond to the metal center assisted by the coordination of L. The metal silicon bond distances in TM-(κ2-L,Si) complexes are in the range of metal-silyl bond distances. TM-(κ2-L,Si) complexes have proven to be effective catalysts for hydrosilylation and/or hydrogenation of unsaturated molecules among other processes.</subfield>
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    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 101034288-IberusExperience</subfield>
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    <subfield code="a">Goméz-España, Alejandra</subfield>
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    <subfield code="a">Fernández-Álvarez, Francisco J.</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Inorgánica</subfield>
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    <subfield code="g">89, 9 (2024), e202400162 [22 pp.]</subfield>
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