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Carbon Dioxide Capture and Functionalization from a Molecular Ti(III) Oxo Anion
Samuel S Veroneau1, Jacob S Mohar1, Mrinal Bhunia1
1Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, PA, 19104, USA.
None:
Carbon dioxide capture and functionalization sequesters carbon dioxide in more robust products and offers a viable route to reducing greenhouse gas emissions. We present herein a unique molecular TiIII oxo anion that reversibly binds CO2 to allow both its sequestration and functionalization. The reduction of [(PN)2Ti═O] (1) [PN = (2-PiiPr2-4-methylphenyl)(mesityl)amide] with KC8 and 2.2.2-cryptand (crypt) resulted in formation of [K(crypt)][(PN)2Ti═O] (2), which was fully characterized and shown to contain a Ti-centered radical. Complex 2 reacts with Al(CH3)3 to form [K(crypt)][(PN)2Ti{O(Al(CH3)3}] (3), which can be independently prepared from [K(crypt)][(PN)2Ti(OCP)] and Al(CH3)3. Whereas 1 does not react with CO2, 2 rapidly captures the gas (1 atm, 25 °C) to produce a TiIII carbonate [K(crypt)][(PN)2Ti(κ2-O2C═O)] (4). Chemical and electrochemical oxidation of 4 releases CO2 to regenerate 1 while a soluble organic carbonate [Me3SiOC(O)OSiMe3, Me = CH3] is obtained from reaction of 4 with ClSiMe3.
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