Metal-organic frameworks from novel flexible triptycene- and pentiptycene-based ligands

被引:17
作者
Crane, Angela K. [1 ]
Wong, Elaine Y. L. [1 ]
MacLachlan, Mark J. [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
COORDINATION POLYMER; GAS-STORAGE; HETEROGENEOUS CATALYST; HYDROGEN ADSORPTION; CRYSTAL; METHANE; DESIGN; GUEST; MOF; MICROPOROSITY;
D O I
10.1039/c3ce41459k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four distinct iptycene-containing metal-organic frameworks (MOFs) were synthesized and characterized using two new organic ligands. By varying the reaction conditions a series of 1-D, 2-D, and 3-D frameworks was synthesized with a range of secondary building units (SBUs) using the same triptycene-derived ligand. Furthermore, the first example of a pentiptycene-containing MOF is reported as an interpenetrated 3-D framework containing pseudo-[Zn4O](6+) clusters. The structural integrity of the MOFs upon guest solvent removal varies depending on the framework, and was tracked using powder X-ray diffraction and thermogravimetric analysis. Gas adsorption experiments were conducted on the robust frameworks and revealed no appreciable surface area. Iptycenyl groups and flexible moieties incorporated into the MOF ligand system appear to enhance structural diversity, but also crowd the pores of the MOF or facilitate framework collapse upon solvent removal, reducing accessible surface area.
引用
收藏
页码:9811 / 9819
页数:9
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