腙
化学
分子
氢键
异构化
光电开关
羧酸
共价键
晶体工程
材料科学
结晶学
单晶
高分子化学
立体化学
光化学
有机化学
催化作用
作者
Rong‐Ran Liang,Jayanta Samanta,Baihao Shao,Mingshi Zhang,Richard J. Staples,Albert D. Chen,Miao Tang,Yuyang Wu,Ivan Aprahamian,Chenfeng Ke
标识
DOI:10.1002/ange.202109987
摘要
Abstract The development of large pore single‐crystalline covalently linked organic frameworks is critical in revealing the detailed structure‐property relationship with substrates. One emergent approach is to photo‐crosslink hydrogen‐bonded molecular crystals. Introducing complementary hydrogen‐bonded carboxylic acid building blocks is promising to construct large pore networks, but these molecules often form interpenetrated networks or non‐porous solids. Herein, we introduced heteromeric carboxylic acid dimers to construct a non‐interpenetrated molecular crystal. Crosslinking this crystal precursor with dithiols afforded a large pore single‐crystalline hydrogen‐bonded crosslinked organic framework H C OF‐101. X‐ray diffraction analysis revealed H C OF‐101 as an interlayer connected hexagonal network, which possesses flexible linkages and large porous channels to host a hydrazone photoswitch. Multicycle Z/E‐isomerization of the hydrazone took place reversibly within H C OF‐101, showcasing the potential use of H C OF‐101 for optical information storage.
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