<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(28)</volume><submitter>Pappuru S</submitter><pubmed_abstract>The conversion of CO&lt;sub>2&lt;/sub> and epoxides to cyclic carbonates over a silica-supported di-iron(III) complex having a reduced Robson macrocycle ligand system is shown to proceed at 1 atm and 80 °C, exclusively producing the &lt;i>cis&lt;/i>-cyclohexene carbonate from cyclohexene oxide. We examine the effect of immobilization configuration to show that the complex grafted in a semirigid configuration catalytically outperforms the rigid, flexible configurations and even the homogeneous counterparts. Using the semirigid catalyst, we are able to obtain a TON of up to 800 and a TOF of up to 37 h&lt;sup>-1&lt;/sup> under 1 atm CO&lt;sub>2&lt;/sub>. The catalyst is shown to be recyclable with only minor leaching and no change to product selectivity. We further examine a range of epoxides with varying electron-w</pubmed_abstract><journal>ACS omega</journal><pagination>24656-24661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9301958</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Atmospheric-Pressure Conversion of CO&lt;sub>2&lt;/sub> to Cyclic Carbonates over Constrained Dinuclear Iron Catalysts.</pubmed_title><pmcid>PMC9301958</pmcid><pubmed_authors>Carmieli R</pubmed_authors><pubmed_authors>Pappuru S</pubmed_authors><pubmed_authors>Shpasser D</pubmed_authors><pubmed_authors>Jentoft FC</pubmed_authors><pubmed_authors>Shekhter P</pubmed_authors><pubmed_authors>Gazit OM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atmospheric-Pressure Conversion of CO&lt;sub>2&lt;/sub> to Cyclic Carbonates over Constrained Dinuclear Iron Catalysts.</name><description>The conversion of CO&lt;sub>2&lt;/sub> and epoxides to cyclic carbonates over a silica-supported di-iron(III) complex having a reduced Robson macrocycle ligand system is shown to proceed at 1 atm and 80 °C, exclusively producing the &lt;i>cis&lt;/i>-cyclohexene carbonate from cyclohexene oxide. We examine the effect of immobilization configuration to show that the complex grafted in a semirigid configuration catalytically outperforms the rigid, flexible configurations and even the homogeneous counterparts. Using the semirigid catalyst, we are able to obtain a TON of up to 800 and a TOF of up to 37 h&lt;sup>-1&lt;/sup> under 1 atm CO&lt;sub>2&lt;/sub>. The catalyst is shown to be recyclable with only minor leaching and no change to product selectivity. We further examine a range of epoxides with varying electron-w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-25T18:15:40.579Z</modification><creation>2025-04-06T07:30:49.715Z</creation></dates><accession>S-EPMC9301958</accession><cross_references><pubmed>35874206</pubmed><doi>10.1021/acsomega.2c02488</doi></cross_references></HashMap>