Abstract
Herein, we report a facile approach towards the construction of poly-functional porous organic polymers (POPs). The functional groups employed were selected to span the range of Lewis-base to neutral to Lewis-acid character. Our results underline the effect of chemical functionality on the observed Q(st) for CO2 adsorption inside the material, being largest for functional groups with electron donating O- and N-centered Lewis base sites. Our systematic investigation within a family of POPs revealed a wide range for CO2 heat of adsorption (23.8-53.8 kJ mol(-1)) that is clearly associated with the chemical nature of the functional groups present. In addition, post-synthetic modification of POPs reported herein demonstrated a facile pathway to dramatically enhance carbon dioxide uptake energetics.