Promising CO₂ Capture and Effective Iodine Adsorption of Hyper-Cross-Linked Conjugated Porous Organic Polymers Prepared from a Cyclopentannulation Reaction

Three novel conjugated porous organic polymers, denoted as C-POP1-3 and which consist of alternating pyrene cores with various contorted fluorene surrogates, were successfully synthesized from a versatile one-pot palladium-catalyzed [3+2] cyclocondensation reaction. The resulting polymers were obtained in excellent yields and displayed weight-average molecular weights (M-w) ranging from 12.2 to 20.2 kg/mol with polydispersity indices (M-w/M-n) ranging between 1.8 and 2.4, suggesting that the molecular masses are narrowly distributed and thus implying homogeneous polymer chains. Thermal stability exploration of C-POP1-3 by thermogravimetric analysis (TGA) revealed an impressive robustness with a 10% weight reduction temperature attaining 485 degrees C. Investigation of the inherent microporosity properties of C-POP1-3 via nitrogen adsorption experiments using Brunauer-Emmett-Teller (BET) theory discloses their surface areas which reach up to 560 m(2) g(-1) and pore volumes averaging 0.47 cm(3) g(-1). The target conjugated polymers were explored as adsorbents disclosing a maximum carbon dioxide adsorption of 83.0 mg g(-1) at 273 K and low pressure for C-POP1, whereas iodine sorption tests portrayed prominent outcomes, notably for C-POP3 which proved to owe a strong affinity toward the hitherto mentioned halogen by achieving a maximum adsorption of 2220 mg g(-1). Additionally, recyclability experiments confirmed the possibility to regenerate the polymers' adsorption capabilities even after seven consecutive cycles of adsorption-desorption cycles, which qualify them as auspicious iodine adsorbents.