American Chemical Society
om3011382_si_001.pdf (5.67 MB)

Reactivity of Dimeric P/Al-Based Lewis Pairs toward Carbon Dioxide and tert-Butyl Isocyanate

Download (5.67 MB)
journal contribution
posted on 2013-11-25, 00:00 authored by Federica Bertini, Frank Hoffmann, Christian Appelt, Werner Uhl, Andreas W. Ehlers, J. Chris Slootweg, Koop Lammertsma
The methylene-bridged phosphinoalane tBu2PCH2AlMe2 exists as a stable, dimeric Lewis adduct, which reacts with carbon dioxide and tert-butyl isocyanate at room temperature, forming five-membered heterocycles; we explored the reaction pathways of these heterocycles with computational chemistry. A carboxylate dimer results when excess carbon dioxide is used. A novel mechanism is presented for this process that presumes the cooperative effect of two CO2 molecules in which the FLP captured CO2 is expelled on insertion of a second molecule into the Al–C bond of the initial heterocycle.