Advancing Magnesium–Organic Porous Materials through New Magnesium Cluster Chemistry
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文摘
While synthesis of materials with novel topologies is important, it can be even more impactful to create new modular structural units capable of serving as a versatile pool of connectors for rational design of targeted solids. Here we report five magnesium–organic frameworks (denoted as CPM-201 to -205) exhibiting step-by-step evolution of trimeric clusters from unprecedented core-less [Mg3(COO)6], to OH-centered [Mg33-OH)(COO)6], and eventually to two variations of pentamers [Mg53-OH)2(COO)8] formed from fusion of trimers. New clusters are joined by dicarboxylates into trigonal-bipyramidal, cuboidal, and octahedral cages embedded in the labyrinth of hexagonal and cubic channels. These materials exhibit high CO2 uptake and CO2/CH4 selectivity.

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