<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Creutz SE</submitter><funding>NIH Office of the Director</funding><funding>Gordon and Betty Moore Foundation</funding><funding>NIGMS NIH HHS</funding><pagination>2321-2328</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5363375</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(3)</volume><pubmed_abstract>Hydrogen bonding and other types of secondary-sphere interactions are ubiquitous in metalloenzyme active sites and are critical to the transformations they mediate. Exploiting secondary sphere interactions in synthetic catalysts to study the role(s) they might play in biological systems, and to develop increasingly efficient catalysts, is an important challenge. Whereas model studies in this broad context are increasingly abundant, as yet there has been relatively little progress in the area of synthetic catalysts for nitrogen fixation that incorporate secondary sphere design elements. Herein we present our first study of Fe-N &lt;sub>&lt;i>x&lt;/i>&lt;/sub> H &lt;sub>&lt;i>y&lt;/i>&lt;/sub> complexes supported by new tris(phosphine)silyl ligands, abbreviated as [SiPNMe3] and [SiPiPr2P&lt;sup>NMe&lt;/sup>], that incorp</pubmed_abstract><journal>Chemical science</journal><pubmed_title>Exploring secondary-sphere interactions in Fe-N &lt;sub>&lt;i>x&lt;/i>&lt;/sub> H &lt;sub>&lt;i>y&lt;/i>&lt;/sub> complexes relevant to N&lt;sub>2&lt;/sub> fixation.</pubmed_title><pmcid>PMC5363375</pmcid><funding_grant_id>GM 070757</funding_grant_id><funding_grant_id>R01 GM070757</funding_grant_id><pubmed_authors>Peters JC</pubmed_authors><pubmed_authors>Creutz SE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploring secondary-sphere interactions in Fe-N &lt;sub>&lt;i>x&lt;/i>&lt;/sub> H &lt;sub>&lt;i>y&lt;/i>&lt;/sub> complexes relevant to N&lt;sub>2&lt;/sub> fixation.</name><description>Hydrogen bonding and other types of secondary-sphere interactions are ubiquitous in metalloenzyme active sites and are critical to the transformations they mediate. Exploiting secondary sphere interactions in synthetic catalysts to study the role(s) they might play in biological systems, and to develop increasingly efficient catalysts, is an important challenge. Whereas model studies in this broad context are increasingly abundant, as yet there has been relatively little progress in the area of synthetic catalysts for nitrogen fixation that incorporate secondary sphere design elements. Herein we present our first study of Fe-N &lt;sub>&lt;i>x&lt;/i>&lt;/sub> H &lt;sub>&lt;i>y&lt;/i>&lt;/sub> complexes supported by new tris(phosphine)silyl ligands, abbreviated as [SiPNMe3] and [SiPiPr2P&lt;sup>NMe&lt;/sup>], that incorp</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2025-04-04T09:01:32.9Z</modification><creation>2019-03-27T02:39:23Z</creation></dates><accession>S-EPMC5363375</accession><cross_references><pubmed>28451336</pubmed><doi>10.1039/c6sc04805f</doi></cross_references></HashMap>