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Preparation of Highly Porous Coordination Polymer Coatings on Macroporous Polymer Monoliths for Enhanced Enrichment of Phosphopeptides
Published on: July 14, 2015
Stimulus-Induced Microflexible Nanopores in Zinc-Based Coordination Network Enable Four Distinct Adsorption
Yi-Tao Li1, Wei-Lin Li2, Li-Ping Zhang1
1State Key Laboratory of Fluorine & Nitrogen Chemicals, National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, China.
Abstract:
Understanding adsorption mechanisms is fundamental to advancing gas separation science and technology. Nevertheless, sorbents that undergo stimulus-induced fine-tuning of their structures to enable multiple adsorption mechanisms are rarely reported. Here, we report that CALF-20, a zinc-based coordination network, exhibits temperature and guest-induced microflexibility to exhibit four distinct and tunable adsorption mechanisms for nine light hydrocarbon gases: (i) thermodynamic selectivity (ethane/ethylene separation); (ii) kinetic-limited adsorption (propane, n-butane, and n-butene); (iii) molecular sieving (iso-butane/iso-butene); (iv) gate-opening flexibility (butadiene capture in the presence of n-alkane impurities). In effect, temperature-dependent structural flexibility enables modulation of guest diffusion kinetics and adsorption thermodynamics. CALF-20 thereby achieves propylene purification from propane and butadiene purification with exceptional selectivity. Structural and computational insights into the mechanisms governing the selective separation of light hydrocarbons using CALF-20 reveal the potential of targeted flexible nanoporous materials with dynamically tunable pore environments, paving the way for next-generation separation technologies in the petrochemical and energy sectors.

