1,3,5-2,4,6-功能化的烯分子:一个对环境有反应的支架,支持层次上的超级结构
Xin-Yu Pang1, Hang Zhou2, Xiaojiang Xie1
1Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, P. R. China.
Angewandte Chemie (International ed. in English)
|June 13, 2024
概括
研究人员开发了一种新型的分子子,可以根据pH值变化在开放和关闭状态之间进行可逆切换. 这种pH触发的运动控制着复杂的层次上的上层结构的组装和拆卸,展示了刺激响应材料的新可能性.
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
- 化学工程是化学工程的重要组成部分.
背景情况:
- 响应刺激的支架对于层次上的超分子组合至关重要.
- 功能化的基分子是宿主分子的建立基石.
- 在多组件超分子结构中使用可切换的基因图案尚未得到充分研究.
研究的目的:
- 报告一种能够产生可逆形状变化的新型分子 (1).
- 为了研究分子的pH诱导的切换机制.
- 为了证明这种子在构建响应刺激的等级超结构中的使用.
主要方法:
- 一个分子子 (1) 的合成,其中包括一个曲的炭二聚物 (3) 和1,3,5-tris(aminomethyl) -2,4,6-triethylbenzene (2).
- 对内的功能化单元的pH诱导异构的研究.
- 在溶液和固体状态下对子的可逆打开和关闭的描述.
- 使用子,形成和分析等级上的超结构,如俄罗斯娃娃般的复合体.
主要成果:
- 一个分子子 (1) 成功合成并证明了可逆的pH触发开放和关闭状态之间的切换.
- 在溶液和固体状态下观察到子的形状运动.
- 使用子形成了响应刺激的等级超结构,包括[K18-crown-61]+和[Kcryptand-2221]+.
- 这些超级结构的组装和拆卸是由子的开放到关闭状态过渡控制的.
结论:
- 这项研究介绍了一种创新的分子子,它利用pH触发的构造运动来控制层次组合的组装.
- 这项工作突出了一个不寻常的机制,即分子构成变化决定了复杂的超分子结构的形成和解离.
- 这些发现为设计超分子化学和材料科学中的可切换支架提供了一个新的范式.
相关概念视频
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
2.2K
Birch reduction uses solvated electrons as reducing agents. The reaction converts benzene to 1,4-cyclohexadiene. The reaction proceeds by the transfer of a single electron to the ring to form a benzene radical anion. This anion is highly basic—it abstracts a proton from the alcohol to form a cyclohexadienyl radical. Another single electron transfer gives the cyclohexadienyl anion. A proton transfer from the alcohol forms 1,4-cyclohexadiene. Since this reduction occurs via radical anion...
2.2K
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
8.0K
Chlorination and bromination are important classes of electrophilic aromatic substitutions, where benzene reacts with chlorine or bromine in the presence of a Lewis acid catalyst to give halogenated substitution products. A Lewis acid such as aluminium chloride or ferric chloride catalyzes the chlorination, and ferric bromide catalyzes the bromination reactions. During the bromination of alkenes, bromine polarizes and becomes electrophilic. However, in the bromination of benzene, the bromine...
8.0K
Structure of Benzene: Molecular Orbital Model
9.0K
According to the molecular orbital (MO) model, benzene has a planar structure with a regular hexagon of six sp2 hybridized carbons. As shown in Figure 1, each carbon is bonded to three other atoms with C–C–C and H–C–C bond angles of 120°. The C–H bond length is 109 pm, and the C–C bond length is 139 pm which is midway between the single bond length of sp3 hybridized carbons (154 pm) and sp2 hybridized carbons (133 pm).
9.0K
Electrophilic Aromatic Substitution: Sulfonation of Benzene
6.0K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
6.0K
Frost Circles for Different Conjugated Systems
2.7K
The inscribed polygon method is consistent with Hückel’s 4n + 2 rule and helps to learn whether the given cyclic compound is aromatic or not. The compound is stable and aromatic if every bonding molecular orbital (MO) is completely filled with a pair of electrons. However, if the non-bonding or antibonding orbitals are filled with electrons, the compound is unstable and not aromatic. Consider the Frost circle diagrams for cycloalkenes containing 4 to 8 carbons.
2.7K
Structure of Benzene: Kekulé Model
8.8K
In 1865, August Kekule suggested the structure of benzene according to the structural theory of organic chemistry based on the three assertions—formula of benzene is C6H6, all the hydrogens of benzene are equivalent, and each carbon must have four bonds due to its tetravalency.
He proposed that benzene has a cyclic structure of six carbon atoms attached to one hydrogen atom each, with three alternating pi bonds.
He proposed that benzene has a cyclic structure of six carbon atoms attached to one hydrogen atom each, with three alternating pi bonds.
8.8K


