<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>60(5)</volume><submitter>Weyer N</submitter><pubmed_abstract>The N-heterocyclic silylene [{Fe(η&lt;sup>5&lt;/sup> -C&lt;sub>5&lt;/sub> H&lt;sub>4&lt;/sub> -NDipp)&lt;sub>2&lt;/sub> }Si] (1DippSi, Dipp=2,6-diisopropylphenyl) shows an excellent combination of pronounced thermal stability and high reactivity towards small molecules. It reacts readily with CO&lt;sub>2&lt;/sub> and N&lt;sub>2&lt;/sub> O, respectively affording (1DippSiO&lt;sub>2&lt;/sub> )&lt;sub>2&lt;/sub> C and (1DippSiO)&lt;sub>2&lt;/sub> as follow-up products of the silanone 1DippSiO. Its reactions with H&lt;sub>2&lt;/sub> O, NH&lt;sub>3&lt;/sub> , and FcPH&lt;sub>2&lt;/sub> (Fc=ferrocenyl) furnish the respective oxidative addition products 1DippSi(H)X (X=OH, NH&lt;sub>2&lt;/sub> , PHFc). Its reaction with H&lt;sub>3&lt;/sub> BNH&lt;sub>3&lt;/sub> unexpectedly results in B-H, instead of N-H, bond activation, affording 1DippSi(H)(BH&lt;sub>2&lt;/sub> NH&lt;sub>3&lt;/sub> ). DFT result</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>2624-2628</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7898919</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Stable N-Heterocyclic Silylene with a 1,1'-Ferrocenediyl Backbone.</pubmed_title><pmcid>PMC7898919</pmcid><pubmed_authors>Heinz M</pubmed_authors><pubmed_authors>Siemeling U</pubmed_authors><pubmed_authors>Weyer N</pubmed_authors><pubmed_authors>Bruhn C</pubmed_authors><pubmed_authors>Schweizer JI</pubmed_authors><pubmed_authors>Holthausen MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Stable N-Heterocyclic Silylene with a 1,1'-Ferrocenediyl Backbone.</name><description>The N-heterocyclic silylene [{Fe(η&lt;sup>5&lt;/sup> -C&lt;sub>5&lt;/sub> H&lt;sub>4&lt;/sub> -NDipp)&lt;sub>2&lt;/sub> }Si] (1DippSi, Dipp=2,6-diisopropylphenyl) shows an excellent combination of pronounced thermal stability and high reactivity towards small molecules. It reacts readily with CO&lt;sub>2&lt;/sub> and N&lt;sub>2&lt;/sub> O, respectively affording (1DippSiO&lt;sub>2&lt;/sub> )&lt;sub>2&lt;/sub> C and (1DippSiO)&lt;sub>2&lt;/sub> as follow-up products of the silanone 1DippSiO. Its reactions with H&lt;sub>2&lt;/sub> O, NH&lt;sub>3&lt;/sub> , and FcPH&lt;sub>2&lt;/sub> (Fc=ferrocenyl) furnish the respective oxidative addition products 1DippSi(H)X (X=OH, NH&lt;sub>2&lt;/sub> , PHFc). Its reaction with H&lt;sub>3&lt;/sub> BNH&lt;sub>3&lt;/sub> unexpectedly results in B-H, instead of N-H, bond activation, affording 1DippSi(H)(BH&lt;sub>2&lt;/sub> NH&lt;sub>3&lt;/sub> ). DFT result</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-05-07T18:38:46.728Z</modification><creation>2021-03-06T08:18:22Z</creation></dates><accession>S-EPMC7898919</accession><cross_references><pubmed>33058389</pubmed><doi>10.1002/anie.202011691</doi></cross_references></HashMap>