<?xml version="1.0" encoding="UTF-8"?>
<collection xmlns="http://www.loc.gov/MARC21/slim">
<record>
  <controlfield tag="001">133413</controlfield>
  <controlfield tag="005">20260217205515.0</controlfield>
  <datafield tag="024" ind1="7" ind2=" ">
    <subfield code="2">doi</subfield>
    <subfield code="a">10.1021/acs.inorgchem.4c00596</subfield>
  </datafield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="2">sideral</subfield>
    <subfield code="a">138073</subfield>
  </datafield>
  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2024-138073</subfield>
  </datafield>
  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Buil, María L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-3284-1053</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Unequivocal characterization of an osmium complex with a terminal sulfide ligand and its transformation into hydrosulfide and methylsulfide</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2024</subfield>
  </datafield>
  <datafield tag="506" ind1="0" ind2=" ">
    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Deprotonation of the thioamidate group of [OsH{κ2-N,S-[NHC(CH3)S]}(≡CPh)(IPr)(PiPr3)]OTf [1; IPr = 1,3-bis(2,6-diisopropylphenyl)imidazolylidene; OTf = CF3SO3] results in the release of acetonitrile and formation of the terminal sulfide complex OsH(S)(≡CPh)(IPr)(PiPr3) (2), which has been transformed into the hydrosulfide [OsH(SH)(≡CPh)(IPr)(PiPr3)]OTf (3) and the methylsulfide [OsH(SMe)(≡CPh)(IPr)(PiPr3)]OTf (4) through protonation and methylation reactions, respectively. The structure, spectroscopic characteristics, and reactivity of these compounds are compared. Reactions of 3 and 4 with 2-hydroxypyridine and 2-mercaptopyridine afford [OsH{κ2-X,N-[X-py]}(≡CPh)(IPr)(PiPr3)]OTf [X = O (5), S(6)].</subfield>
  </datafield>
  <datafield tag="536" ind1=" " ind2=" ">
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/E06-23R</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN-AEI/10.13039/501100011033</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2020-115286GB-I00/AEI/10.13039/501100011033</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/RED2022-134287-T</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by</subfield>
    <subfield code="u">https://creativecommons.org/licenses/by/4.0/deed.es</subfield>
  </datafield>
  <datafield tag="590" ind1=" " ind2=" ">
    <subfield code="a">4.7</subfield>
    <subfield code="b">2024</subfield>
  </datafield>
  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">CHEMISTRY, INORGANIC &amp; NUCLEAR</subfield>
    <subfield code="b">6 / 43 = 0.14</subfield>
    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
  </datafield>
  <datafield tag="592" ind1=" " ind2=" ">
    <subfield code="a">0.958</subfield>
    <subfield code="b">2024</subfield>
  </datafield>
  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Chemistry (miscellaneous)</subfield>
    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
  </datafield>
  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Physical and Theoretical Chemistry</subfield>
    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
  </datafield>
  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Inorganic Chemistry</subfield>
    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
  </datafield>
  <datafield tag="594" ind1=" " ind2=" ">
    <subfield code="a">7.4</subfield>
    <subfield code="b">2024</subfield>
  </datafield>
  <datafield tag="655" ind1=" " ind2="4">
    <subfield code="a">info:eu-repo/semantics/article</subfield>
    <subfield code="v">info:eu-repo/semantics/publishedVersion</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Esteruelas, Miguel A.</subfield>
    <subfield code="0">(orcid)0000-0002-4829-7590</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Oñate, Enrique</subfield>
    <subfield code="0">(orcid)0000-0003-2094-719X</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Picazo, Nieves R.</subfield>
  </datafield>
  <datafield tag="710" ind1="2" ind2=" ">
    <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>
  </datafield>
  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">63, 13 (2024), 4 pp.</subfield>
    <subfield code="p">Inorg. chem.</subfield>
    <subfield code="t">Inorganic Chemistry</subfield>
    <subfield code="x">0020-1669</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="s">1418737</subfield>
    <subfield code="u">http://zaguan.unizar.es/record/133413/files/texto_completo.pdf</subfield>
    <subfield code="y">Versión publicada</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="s">3287792</subfield>
    <subfield code="u">http://zaguan.unizar.es/record/133413/files/texto_completo.jpg?subformat=icon</subfield>
    <subfield code="x">icon</subfield>
    <subfield code="y">Versión publicada</subfield>
  </datafield>
  <datafield tag="909" ind1="C" ind2="O">
    <subfield code="o">oai:zaguan.unizar.es:133413</subfield>
    <subfield code="p">articulos</subfield>
    <subfield code="p">driver</subfield>
  </datafield>
  <datafield tag="951" ind1=" " ind2=" ">
    <subfield code="a">2026-02-17-20:26:44</subfield>
  </datafield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">ARTICLE</subfield>
  </datafield>
</record>
</collection>