Copolymers bearing DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) and DBN (1,5-diazabicyclo[4.3.0]non-5-ene) moieties fixed carbon dioxide under atmospheric pressure. The copolymers bearing DBN moieties fixed carbon dioxide faster than those bearing DBU moieties owing to the lower steric hindrance around the imine structure. These copolymers held trapped CO 2 under a N 2 flow at 25 °C, whereas the corresponding low-molecular weight amidines release trapped CO 2 under the same conditions. The trapped CO 2 in the copolymers was quantitatively released by a N 2 flow at 120 °C. The CO 2 trapping efficiency of a copolymer bearing DBN moieties is competitive with that of an amidine-containing polymer, whereas the preparative method for the copolymer bearing DBN is easier. The higher CO 2 trapping abilities of the DBN derivatives were supported by computational calculation.
No takes yet. Share an insight, caveat, or question.
Ochiai et al. (2008) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: