<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu HY</submitter><funding>Royal Commission for the Exhibition of 1851</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>17851-17856</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8554760</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>143(42)</volume><pubmed_abstract>Sodium reduction of [{SiN&lt;sup>Dipp&lt;/sup>}Mg] [{SiN&lt;sup>Dipp&lt;/sup>} = {CH&lt;sub>2&lt;/sub>SiMe&lt;sub>2&lt;/sub>N(Dipp)}&lt;sub>2&lt;/sub>; Dipp = 2,6-&lt;i>i-&lt;/i>Pr&lt;sub>2&lt;/sub>C&lt;sub>6&lt;/sub>H&lt;sub>3&lt;/sub>] provides the Mg(I) species, [{SiN&lt;sup>Dipp&lt;/sup>}MgNa]&lt;sub>2&lt;/sub>, in which the long Mg-Mg bond (>3.2 Å) is augmented by persistent Na-aryl interactions. Computational assessment indicates that this molecule is best considered to comprise a contiguous tetrametallic core, a viewpoint borne out by its reaction with CO, which results in ethynediolate formation mediated by the dissimilar metal centers.</pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>Reductive Dimerization of CO by a Na/Mg(I) Diamide.</pubmed_title><pmcid>PMC8554760</pmcid><funding_grant_id>EP/R020752/1</funding_grant_id><pubmed_authors>McMullin CL</pubmed_authors><pubmed_authors>Liu HY</pubmed_authors><pubmed_authors>Hill MS</pubmed_authors><pubmed_authors>Schwamm RJ</pubmed_authors><pubmed_authors>Neale SE</pubmed_authors><pubmed_authors>Mahon MF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reductive Dimerization of CO by a Na/Mg(I) Diamide.</name><description>Sodium reduction of [{SiN&lt;sup>Dipp&lt;/sup>}Mg] [{SiN&lt;sup>Dipp&lt;/sup>} = {CH&lt;sub>2&lt;/sub>SiMe&lt;sub>2&lt;/sub>N(Dipp)}&lt;sub>2&lt;/sub>; Dipp = 2,6-&lt;i>i-&lt;/i>Pr&lt;sub>2&lt;/sub>C&lt;sub>6&lt;/sub>H&lt;sub>3&lt;/sub>] provides the Mg(I) species, [{SiN&lt;sup>Dipp&lt;/sup>}MgNa]&lt;sub>2&lt;/sub>, in which the long Mg-Mg bond (>3.2 Å) is augmented by persistent Na-aryl interactions. Computational assessment indicates that this molecule is best considered to comprise a contiguous tetrametallic core, a viewpoint borne out by its reaction with CO, which results in ethynediolate formation mediated by the dissimilar metal centers.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-19T15:35:11.096Z</modification><creation>2025-04-19T15:35:11.096Z</creation></dates><accession>S-EPMC8554760</accession><cross_references><pubmed>34652134</pubmed><doi>10.1021/jacs.1c09467</doi></cross_references></HashMap>