National Creative Research Initiative Center for Smart Supramolecules, Department of Chemistry, and Division of Advanced Materials Science, Pohang University of Science and Technology, San 31 Hyojadong, Pohang 790-784, Republic of Korea.
J Am Chem Soc. 2010 Sep 8;132(35):12200-2. doi: 10.1021/ja105211w.
The organic molecular porous material 1 obtained by recrystallization of cucurbit[6]uril (CB[6]) from HCl shows a high CO(2) sorption capacity at 298 K, 1 bar. Most interestingly, 1 showed the highest selectivity of CO(2) over CO among the known porous materials so far. The remarkable selectivity of CO(2) may be attributed to the exceptionally high enthalpy of adsorption (33.0 kJ/mol). X-ray crystal structure analysis of CO(2) adsorbed 1 revealed three independent CO(2) sorption sites: two in the 1D channels (A and B) and one in the molecular cavities (C). The CO(2) molecules adsorbed at sorption site A near the wall of the 1D channels interact with 1 through hydrogen bonding and at the same time interact with those at site B mainly through quadrupole-quadrupole interaction in a T-shaped arrangement. Interestingly, two CO(2) molecules are included in the CB[6] cavity (site C), interacting not only with the carbonyl groups of CB[6] but also with each other in a slipped-parallel geometry. The exceptionally selective CO(2) sorption properties of 1 may find useful applications in the pressure swing adsorption (PSA) process for CO(2) separation not only in the steel industry but also in other industries such as natural gas mining.
通过从 HCl 中重结晶葫芦脲(CB[6])得到的有机分子多孔材料 1 在 298 K、1 bar 下表现出高的 CO(2)吸附容量。最有趣的是,1 在迄今为止已知的多孔材料中表现出对 CO(2)的最高选择性。CO(2)的显著选择性可能归因于极高的吸附焓(33.0 kJ/mol)。吸附 CO(2)的 1 的 X 射线晶体结构分析揭示了三个独立的 CO(2)吸附位点:一个在 1D 通道(A 和 B)中,一个在分子腔(C)中。吸附在 1D 通道壁附近的吸附位 A 的 CO(2)分子通过氢键与 1 相互作用,同时与位于 B 位的 CO(2)分子主要通过四极矩-四极矩相互作用以 T 型排列相互作用。有趣的是,两个 CO(2)分子被包含在 CB[6]腔中(位 C),不仅与 CB[6]的羰基相互作用,而且以滑移平行的几何形状彼此相互作用。1 对 CO(2)的高选择性吸附性能可能在压力摆动吸附(PSA)过程中用于 CO(2)分离,不仅在钢铁行业,而且在天然气开采等其他行业也有应用。