<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(47)</volume><submitter>Witteman L</submitter><pubmed_abstract>A computationally guided synthetic route to a free silanide derived from tris(3-methylindol-2-yl)methane ([(tmim)Si]&lt;sup>-&lt;/sup> ) through nucleophilic substitution on the Si&lt;sup>II&lt;/sup> precursor (Idipp)SiCl&lt;sub>2&lt;/sub> is reported (Idipp=2,3-dihydro-1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-2-ylidene). This approach circumvents the need for strained tetrahedral silanes as synthetic intermediates. Computational investigations show that the electron-donating properties of [(tmim)Si]&lt;sup>-&lt;/sup> are close to those of PMe&lt;sub>3.&lt;/sub> Experimentally, the [(tmim)Si]&lt;sup>-&lt;/sup> anion is shown to undergo clean complexation to the base metal salts CuCl and FeCl&lt;sub>2&lt;/sub> , demonstrating the potential utility as a supporting ligand.</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pagination>12236-12240</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6120461</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Free Silanide from Nucleophilic Substitution at Silicon(II).</pubmed_title><pmcid>PMC6120461</pmcid><pubmed_authors>Moret ME</pubmed_authors><pubmed_authors>Evers T</pubmed_authors><pubmed_authors>Witteman L</pubmed_authors><pubmed_authors>Lutz M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Free Silanide from Nucleophilic Substitution at Silicon(II).</name><description>A computationally guided synthetic route to a free silanide derived from tris(3-methylindol-2-yl)methane ([(tmim)Si]&lt;sup>-&lt;/sup> ) through nucleophilic substitution on the Si&lt;sup>II&lt;/sup> precursor (Idipp)SiCl&lt;sub>2&lt;/sub> is reported (Idipp=2,3-dihydro-1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-2-ylidene). This approach circumvents the need for strained tetrahedral silanes as synthetic intermediates. Computational investigations show that the electron-donating properties of [(tmim)Si]&lt;sup>-&lt;/sup> are close to those of PMe&lt;sub>3.&lt;/sub> Experimentally, the [(tmim)Si]&lt;sup>-&lt;/sup> anion is shown to undergo clean complexation to the base metal salts CuCl and FeCl&lt;sub>2&lt;/sub> , demonstrating the potential utility as a supporting ligand.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2021-02-21T07:46:21Z</modification><creation>2019-03-26T23:54:48Z</creation></dates><accession>S-EPMC6120461</accession><cross_references><pubmed>29577491</pubmed><doi>10.1002/chem.201801435</doi></cross_references></HashMap>