Dipeptide Crystals as Excellent Permselective Materials: Sequential Exclusion of Argon, Nitrogen, and Oxygen
Dipeptide Crystals as Excellent Permselective Materials: Sequential Exclusion of Argon, Nitrogen, and Oxygen
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DOI:
10.1002/anie.201000007
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发表时间:
2010-01-01
影响因子:
16.6
通讯作者:
Gales, Luis
中科院分区:
文献类型:
--
作者:
Afonso, Rui V.;Durao, Joana;Gales, Luis
Gas storage and gas separation using porous solids are important technologies that have attracted great attention because of their environmental and energetic applications. Highly porous materials, such as zeolites, silicate, and carbonbased materials,[1] have long-established specific applications. The key for new applications is the development of new frameworks. Advances in gas sorption capacities were achieved through the synthesis of materials such as metal–organic frameworks (MOFs), organic polymers, and microporous organic crystals.[2] Recently, crystals formed by dipeptides were tested as adsorbents [3] with significant results in hydrogen absorption and methane purification from carbon dioxide.[3b]Dipeptides can form microporous materials with channels of tunable size. Although the dipeptides self-assemble through a net of hydrogen bonds, the crystal matrix is conserved upon exchange of guest molecules. Moreover, crystalline dipeptides show a very high density of single-size micropores with very low tortuosity, which makes them excellent materials for storage or selective separation purposes. Finally, there is the remarkable feature that pores of crystalline dipeptides are perfectly aligned (along the crystallographic c axis), which indicates that they are excellent candidates for use as permeation-selective barriers. Herein, we report for the first time the use of dipeptide crystals as permselective materials. Although this looks like an obvious engineering application for the kind of porous topology present in the crystals, there are issues that call for experimental support: 1) potential crystal defects, such as twinning or fractures, may greatly diminish their actual selectivity; and 2) the potential lack of rigidity of the crystal structure allows the pores to adapt to some extent to the size of the guest molecules. The dynamic behavior of the matrix of