灵活的共价有机支柱的状自我分类,用于自适应分子识别
Shengnan Gao1, Min Zhang1, Yimin Zhang1
1Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) and College of Chemistry and Chemical Engineering, Xiamen University, 422 Siming South Road, Siming District, Xiamen, 361005, P.R. China.
Angewandte Chemie (International ed. in English)
|June 8, 2025
概括
灵活的共价有机支柱 (flex-COP) 是新的纳米管状宿主,它们的形状适应客分子. 它们的组装表现出奇偶效应,使得精确的分子识别和模仿生物受体成为可能.
科学领域:
- 超分子化学 超分子化学
- 材料科学 材料科学 材料科学
- 有机化学 有机化学
背景情况:
- 柱状烯宏循环是超分子结构的关键组成部分.
- 动态共价化学可以构建适应性的分子架构.
- 具有可调节通道的分子容器对于宿主-客人化学是必不可少的.
研究的目的:
- 引入灵活的共价有机支柱 (flex-COP-n) 作为新的纳米管状宿主.
- 为了研究flex-COP-n.的自我组装行为和主机-客户属性.
- 探索形状灵活性在狭小空间内的分子识别中的作用.
主要方法:
- 用于flex-COP-n合成的动态胺凝结.
- 核磁共振光谱用于研究宿主与客人的相互作用.
- 单晶X射线晶体学用于结构确定.
主要成果:
- 柔性-COP-n化合物已经成功地合成了双开端纳米管状结构.
- 在自我组装过程中观察到一个明显的奇偶效应,导致奇拉或中等双重.
- 宿主-客人与二甲基的复合揭示了各种结合模式,从放松到紧张,由于几何互补性和变形.
结论:
- 符合性灵活性对于调节纳米级限制中的分子识别至关重要.
- Flex-COP-n代表了一个动态的平台,用于创建具有适应能力的分子受体,灵感来自生物系统.
相关概念视频
Molecules with Multiple Chiral Centers
12.6K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
12.6K
Prochirality
4.0K
The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
4.0K
Chirality at Nitrogen, Phosphorus, and Sulfur
6.0K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
6.0K
Chirality
25.7K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
25.7K
Chirality in Nature
14.0K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
14.0K
Molecular Shape and Polarity
62.3K
Dipole Moment of a Molecule
62.3K


