Abstract

We present a spin-crossover Fe<sup>II</sup> coordination polymer with no permanent channels that selectively sorbs CO<sub>2</sub> over N<sub>2</sub>. The one-dimensional chains display internal voids of ∼9 Å diameter, each being capable to accept one molecule of CO<sub>2</sub> at 1 bar and 273 K. X-ray diffraction provides direct structural evidence of the location of the gas molecules and reveals the formation of OCO­(δ<sup>–</sup>)···π interactions. This physisorption modifies the spin transition, producing a 9 K increase in <i>T</i><sub>1/2</sub>

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