Optimizing bromide anchors for easy tethering of amines, nitriles and thiols in porous organic polymers towards enhanced CO2 capture

Vepa Rozyyev, Mustafa S. Yavuz, Damien Thirion, Thien Si Nguyen, Thi Phuong Nga Nguyen, Abdul-Hamid M. Emwas, Cafer T. Yavuz

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

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.
Original languageEnglish (US)
Pages (from-to)111450
JournalMicroporous and Mesoporous Materials
DOIs
StatePublished - Sep 21 2021

ASJC Scopus subject areas

  • Mechanics of Materials
  • General Materials Science
  • General Chemistry
  • Condensed Matter Physics

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