Highly controlled acetylene accommodation in a metal-organic microporous material
Highly controlled acetylene accommodation in a metal-organic microporous material
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DOI:
10.1038/nature03852
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发表时间:
2005-07-14
期刊:
影响因子:
64.8
通讯作者:
Mita, Y
中科院分区:
文献类型:
--
作者:
Matsuda, R;Kitaura, R;Mita, Y
Metal - organic microporous materials(1-4) (MOMs) have attracted wide scientific attention owing to their unusual structure and properties, as well as commercial interest due to their potential applications in storage(5-9), separation(10,11) and heterogeneous catalysis(12,13). One of the advantages of MOMs compared to other microporous materials, such as activated carbons, is their ability to exhibit a variety of pore surface properties such as hydrophilicity and chirality, as a result of the controlled incorporation of organic functional groups into the pore walls(11,13-15). This capability means that the pore surfaces of MOMs could be designed to adsorb specific molecules; but few design strategies for the adsorption of small molecules have been established so far. Here we report high levels of selective sorption of acetylene molecules as compared to a very similar molecule, carbon dioxide, onto the functionalized surface of a MOM. The acetylene molecules are held at a periodic distance from one another by hydrogen bonding between two non-coordinated oxygen atoms in the nanoscale pore wall of the MOM and the two hydrogen atoms of the acetylene molecule. This permits the stable storage of acetylene at a density 200 times the safe compression limit of free acetylene at room temperature.