<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Widemann M</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>e202201032</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9541956</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(45)</volume><pubmed_abstract>Following the alkane-elimination route, the reaction between tetravalent aryl tintrihydride Ar*SnH&lt;sub>3&lt;/sub> and trivalent rare-earth-metallocene alkyls [Cp*&lt;sub>2&lt;/sub> Ln(CH{SiMe&lt;sub>3&lt;/sub> }&lt;sub>2&lt;/sub> )] gave complexes [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> SnAr*] implementing a low-valent tin hydride (Ln=Y, Lu; Ar*=2,6-Trip&lt;sub>2&lt;/sub> C&lt;sub>6&lt;/sub> H&lt;sub>3&lt;/sub> , Trip=2,4,6-triisopropylphenyl). The homologous complexes of germanium and lead, [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> EAr*] (E = Ge, Pb), were accessed via addition of low-valent [(Ar*EH)&lt;sub>2&lt;/sub> ] to the rare-earth-metal hydrides [(Cp*&lt;sub>2&lt;/sub> LnH)&lt;sub>2&lt;/sub> ]. The lead compounds [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> PbAr*] exhibit H/D exchange in reactions with deuterated solvents or dihydrogen.</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>Molecular Ln(III)-H-E(II) Linkages (Ln=Y, Lu; E=Ge, Sn, Pb).</pubmed_title><pmcid>PMC9541956</pmcid><funding_grant_id>WE 1876/13-1</funding_grant_id><pubmed_authors>Eichele K</pubmed_authors><pubmed_authors>Maichle-Mossmer C</pubmed_authors><pubmed_authors>Bonath M</pubmed_authors><pubmed_authors>Schubert H</pubmed_authors><pubmed_authors>Aicher FSW</pubmed_authors><pubmed_authors>Sirsch P</pubmed_authors><pubmed_authors>Anwander R</pubmed_authors><pubmed_authors>Widemann M</pubmed_authors><pubmed_authors>Wesemann L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Ln(III)-H-E(II) Linkages (Ln=Y, Lu; E=Ge, Sn, Pb).</name><description>Following the alkane-elimination route, the reaction between tetravalent aryl tintrihydride Ar*SnH&lt;sub>3&lt;/sub> and trivalent rare-earth-metallocene alkyls [Cp*&lt;sub>2&lt;/sub> Ln(CH{SiMe&lt;sub>3&lt;/sub> }&lt;sub>2&lt;/sub> )] gave complexes [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> SnAr*] implementing a low-valent tin hydride (Ln=Y, Lu; Ar*=2,6-Trip&lt;sub>2&lt;/sub> C&lt;sub>6&lt;/sub> H&lt;sub>3&lt;/sub> , Trip=2,4,6-triisopropylphenyl). The homologous complexes of germanium and lead, [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> EAr*] (E = Ge, Pb), were accessed via addition of low-valent [(Ar*EH)&lt;sub>2&lt;/sub> ] to the rare-earth-metal hydrides [(Cp*&lt;sub>2&lt;/sub> LnH)&lt;sub>2&lt;/sub> ]. The lead compounds [Cp*&lt;sub>2&lt;/sub> Ln(μ-H)&lt;sub>2&lt;/sub> PbAr*] exhibit H/D exchange in reactions with deuterated solvents or dihydrogen.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-22T12:06:34.248Z</modification><creation>2025-04-06T00:14:58.311Z</creation></dates><accession>S-EPMC9541956</accession><cross_references><pubmed>35620817</pubmed><doi>10.1002/chem.202201032</doi></cross_references></HashMap>