笼子
对映体药物
超分子化学
钛
Crystal(编程语言)
单晶
胺气处理
化学
氢键
结晶学
材料科学
晶体结构
有机化学
分子
对映选择合成
催化作用
数学
程序设计语言
组合数学
计算机科学
作者
Yan‐Ping He,Guang‐Hui Chen,De‐Jing Li,Qiaohong Li,Lei Zhang,Jian Zhang
标识
DOI:10.1002/anie.202013977
摘要
Abstract Many metal–organic cages (MOCs) and a few hydrogen‐bonded organic cages (HOCs) have been investigated, but little is reported about cooperative self‐assembly of MOCs and HOCs. Herein, we describe an unprecedented MOC&HOC co‐crystal composed of tetrahedral Ti 4 L 6 (L=embonate) cages and in‐situ‐generated [(NH 3 ) 4 (TIPA) 4 ] (TIPA=tris(4‐(1 H ‐1,2,4‐triazol‐1‐yl)phenyl)amine) cages. Chiral transfer is observed from the enantiopure Ti 4 L 6 cage to enantiopure [(NH 3 ) 4 (TIPA) 4 ] cage. Two homochiral supramolecular frameworks with opposite handedness ( PTC‐235(Δ) and PTC‐235(Λ) ) are formed. Such MOC&HOC co‐crystal features high stability in water and other solvents, affording single‐crystal‐to‐single‐crystal transformation to trap CH 3 CN molecules and identify disordered NH 4 + cations. A tablet pressing method is developed to test the third‐order nonlinear optical property of KBr‐based PTC‐235 thin film. Such a thin film exhibits an excellent optical limiting effect.
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