TY - JOUR
T1 - Optimizing bromide anchors for easy tethering of amines, nitriles and thiols in porous organic polymers towards enhanced CO2 capture
AU - Rozyyev, Vepa
AU - Yavuz, Mustafa S.
AU - Thirion, Damien
AU - Nguyen, Thien Si
AU - Nga Nguyen, Thi Phuong
AU - Emwas, Abdul-Hamid M.
AU - Yavuz, Cafer T.
N1 - KAUST Repository Item: Exported on 2021-09-28
Acknowledgements: This work was supported by National Research Foundation of Korea (NRF) grants funded by the Korean government (MSIP) (No. NRF-2017M3A7B4042140 and NRF-2017M3A7B4042235) and the startup funds by the King Abdullah University of Science and Technology (KAUST).
PY - 2021/9/21
Y1 - 2021/9/21
N2 - Porous organic polymers with labile leaving groups offer direct access to reactive functional groups, otherwise not permissible during network formation. In a one-step, open air, self-coupling reaction of tris bromomethyl benzene, we report highly porous, bromine rich C–C bonded porous polymers. Due to the steric nature of the monomer, restrictive crosslinking allowed pendent bromine groups to remain unreacted and provided rapid exchange into amines, nitriles, and thiols. This simple but powerful strategy yielded two isostructural but varying porosity and pendent group density polymers, allowing a comparative gas uptake study. Despite having lower surface area, the porous polymer formed at low temperature showed higher amination due to higher density of bromine groups. The polymers with more pendant groups resulted better CO2 uptake performances than higher porosity polymers with less pendant groups. Although post-modification decreased surface area of materials, amine functionalization greatly improved the CO2 uptake capacity. The ethylenediamine appended version exhibited 4.7 times increase in CO2 uptake capacity with highest CO2/N2 selectivity of 729 (298 K), and with an isosteric heat of 97 kJ mol−1 at zero coverage.
AB - Porous organic polymers with labile leaving groups offer direct access to reactive functional groups, otherwise not permissible during network formation. In a one-step, open air, self-coupling reaction of tris bromomethyl benzene, we report highly porous, bromine rich C–C bonded porous polymers. Due to the steric nature of the monomer, restrictive crosslinking allowed pendent bromine groups to remain unreacted and provided rapid exchange into amines, nitriles, and thiols. This simple but powerful strategy yielded two isostructural but varying porosity and pendent group density polymers, allowing a comparative gas uptake study. Despite having lower surface area, the porous polymer formed at low temperature showed higher amination due to higher density of bromine groups. The polymers with more pendant groups resulted better CO2 uptake performances than higher porosity polymers with less pendant groups. Although post-modification decreased surface area of materials, amine functionalization greatly improved the CO2 uptake capacity. The ethylenediamine appended version exhibited 4.7 times increase in CO2 uptake capacity with highest CO2/N2 selectivity of 729 (298 K), and with an isosteric heat of 97 kJ mol−1 at zero coverage.
UR - http://hdl.handle.net/10754/672001
UR - https://linkinghub.elsevier.com/retrieve/pii/S138718112100576X
U2 - 10.1016/j.micromeso.2021.111450
DO - 10.1016/j.micromeso.2021.111450
M3 - Article
SN - 1387-1811
SP - 111450
JO - Microporous and Mesoporous Materials
JF - Microporous and Mesoporous Materials
ER -