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    <subfield code="a">10.1002/ejic.202200163</subfield>
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    <subfield code="a">Gimeno-Prat, A.</subfield>
    <subfield code="0">(orcid)0000-0001-9071-4506</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Trans-amidate platinum complexes anchoring water and N-donor molecules. The importance of hydrogen bonding</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2022</subfield>
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    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">The square planar bisnitrile platinum(II) derivatives PtCl2(NCR)2 (R=Ph (1 a); Et (1 b); p-C6H4F (1 c); p-C6H4tBu (1 d); m-C6H3Me2 (1 e); o, p-C6H2Me3 (1 f)) react with tetrabutylammonium hydroxide to render the monoaquo NBu4]trans-PtCl(HNCOR)2(OH2)] (2 a–2 f). The water molecule is s-coordinated to platinum and the binding is reinforced by two strong hydrogen bonds to the neighboring amidate ligands (OH···OC). Substitution of water in 2 a by N-donor ligands can be efficiently achieved only in the presence of a dehydrating agent as magnesium sulphate or 4 Å molecular sieves. By following this strategy, compounds NBu4]trans-PtCl(HNCOPh)2(NH2R’)] (R’=H (3), NH2 (4), tBu (5 a), p-C6H4Me (5 b) have been isolated. The incoming ligands are s-coordinated to platinum and also establish strong hydrogen bonds to the amidates (NH···OC). Treatment of 2 a with halogens causes oxidation at the metal center, rendering the platinum(IV) derivatives NBu4]PtClX2(HNCOPh)2(OH2)] (X=Cl (6 a), Br (6 b), I (6 c)).</subfield>
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    <subfield code="b">21 / 42 = 0.5</subfield>
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    <subfield code="a">Inorganic Chemistry</subfield>
    <subfield code="c">2022</subfield>
    <subfield code="d">Q2</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Martín, A.</subfield>
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    <subfield code="a">Baya, M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-2492-625X</subfield>
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    <subfield code="a">Casas, J. M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-0341-7699</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="g">2022, 22 (2022), e202200163 [8 pp.]</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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