Abstract:
Herein an ionic Zn(II)–porphyrin complex, [Zn(II)NMeTPyP]4+[I ]4 (Zn(II)
NMeTPyP ¼ 5,10,15,20-tetrakis(1-methylpyridinium-40
-yl) zinc(II)
porphyrin), was immobilized in a porous metal–organic framework,
PCN-224. The resulting [Zn(II)NMeTPyP]4+[I ]4@PCN-224 hybrid was
thoroughly characterized by PXRD, UV-vis, FTIR, MP-AES, SEM-EDS
and BET analysis. Further, DFT calculations confirmed the incorporation of the [Zn(II)NMeTPyP]4+[I ]4 complex in the 1D channels of PCN224 owing to appropriate matching of the pore size with the size of the
complex and stabilization via p–p interactions. Interestingly, the [Zn(II)
NMeTPyP]4+[I ]4@PCN-224 hybrid showed high affinity for CO2 with
a high heat of adsorption (Qst) value of 40.5 kJ mol 1 compared to the
pristine MOF, PCN-224, with a Qst value of 36.8 kJ mol 1
. Remarkably,
the hybrid material acts as an efficient environment-friendly, cocatalyst- and solvent-free heterogeneous catalyst for chemical fixation of CO2 to generate cyclic carbonates with high yield and selectivity due to synergistic cooperation between the complex and the
framework.
