Modulating supramolecular binding of carbon dioxide in a redox-active porous metal-organic framework

Zhenzhong Lu, Harry G. W. Godfrey, Iván da Silva, Yongqiang Cheng, Mathew Savage, Floriana Tuna, Eric J. L. McInnes, Simon J. Teat, Kevin J. Gagnon, Mark D. Frogley,

Nature Communications · 2017 · 88 citations · 27 references

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Abstract

Hydrogen bonds dominate many chemical and biological processes, and chemical modification enables control and modulation of host-guest systems. Here we report a targeted modification of hydrogen bonding and its effect on guest binding in redox-active materials. MFM-300(V<sup>III</sup>) {[V<sup>III</sup><sub>2</sub>(OH)<sub>2</sub>(L)], LH<sub>4</sub>=biphenyl-3,3',5,5'-tetracarboxylic acid} can be oxidized to isostructural MFM-300(V<sup>IV</sup>), [V<sup>IV</sup><sub>2</sub>O<sub>2</sub>(L)], in which deprotonation of the bridging hydroxyl groups occurs. MFM-300(V<sup>III</sup>) shows the second highest CO<sub>2</sub> uptake capacity in metal-organic framework materials at 298 K and 1 bar (6.0 mmol g<sup>-1</sup>) and involves hydrogen bonding between the OH group of the host and the O-donor of CO<sub>2</sub>, which binds in an end-on manner, =1.863(1) Å. In contrast, CO<sub>2</sub>-loaded MFM-300(V<sup>IV</sup>) shows CO<sub>2</sub> bound side-on to the oxy group and sandwiched between two phenyl groups involving a unique ···c.g.<sub>phenyl</sub> interaction [3.069(2), 3.146(3) Å]. The macroscopic packing of CO<sub>2</sub> in the pores is directly influenced by these primary binding sites.

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