化学
脱氢
苯
氢键
超分子化学
选择性
吸附
热稳定性
氢
酰胺
溶剂
高分子化学
多孔性
有机化学
无机化学
晶体结构
分子
催化作用
作者
Jian Lü,Cristina Perez Krap,Mikhail Suyetin,Nada H. Alsmail,Yong Yan,Sihai Yang⧫,William Lewis,Elena Bichoutskaia,Chiu C. Tang,Alexander J. Blake,Rong Cao,Martin Schröder
摘要
A robust binary hydrogen-bonded supramolecular organic framework (SOF-7) has been synthesized by solvothermal reaction of 1,4-bis-(4-(3,5-dicyano-2,6-dipyridyl)dihydropyridyl)benzene (1) and 5,5'-bis-(azanediyl)-oxalyl-diisophthalic acid (2). Single crystal X-ray diffraction analysis shows that SOF-7 comprises 2 and 1,4-bis-(4-(3,5-dicyano-2,6-dipyridyl)pyridyl)benzene (3); the latter formed in situ from the oxidative dehydrogenation of 1. SOF-7 shows a three-dimensional four-fold interpenetrated structure with complementary O-H···N hydrogen bonds to form channels that are decorated with cyano and amide groups. SOF-7 exhibits excellent thermal stability and solvent and moisture durability as well as permanent porosity. The activated desolvated material SOF-7a shows high CO2 adsorption capacity and selectivity compared with other porous organic materials assembled solely through hydrogen bonding.
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