光响应性结合分子网络,能够在异构化后保持晶体周期性
Koki Kasuya1, Ryusei Oketani1, Souta Matsuda2
1Division of Chemistry, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, 560-8531, Toyonaka, Osaka, Japan.
Angewandte Chemie (International ed. in English)
|April 5, 2024
概括
研究人员使用联网开发了一种新的光色多孔晶体. 这种晶体框架在光异构化后保持其结构,为新的光驱动功能材料铺平了道路.
科学领域:
- 材料科学 材料科学 材料科学
- 晶体学 晶体学是指结晶学.
- 有机化学 有机化学
背景情况:
- 光色有机晶体通过光辐射提供可调节的特性,但创建允许光诱导运动的多孔晶体框架是具有挑战性的.
- 现有的光色材料往往缺乏先进应用所需的有序,多孔结构.
研究的目的:
- 设计和表征一种具有键网络的新型光响应单晶.
- 为了研究光异构化行为和晶体状态的结构变化.
- 为了证明创建保持晶体周期性的光色多孔框架的潜力.
主要方法:
- 一种二二甲基子[e]烯衍生物 (4BDHP) 的合成.
- 对H结合网络 (4BDHP-2) 的晶体结构分析.
- 照相辐射实验在化纯晶体 ((S,S) -4BDHP-2) 上,以诱导异构化.
- 通过X射线衍射来确定光异构化晶体的结构.
主要成果:
- 基于H-结合波浪层的光响应单晶 (4BDHP-2) 已成功合成.
- 光异构化发生在晶体状态下,在封闭 (4BDHP) 和开放 (4CPD) 形式之间进行过渡.
- 纯晶体结构揭示了封闭和开放形式的交替排列,同时保持了晶体周期性.
- 在光异构化过程中观察到副作用的证据.
结论:
- 开发了一种概念验证的光色框架晶体,证明了在晶体状态内控制的光异构化.
- 在光异构化后保持晶体周期性的能力为光驱动的多孔功能材料开辟了可能性.
- 这项研究为设计具有有序网络结构的先进光色材料提供了基础.
更多相关视频
相关概念视频
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
834
At room temperature, the chair conformer of cyclohexane undergoes rapid ring flipping between two equivalent chair conformers at a rate of approximately 105 times per second. These two chair conformers are in equilibrium. The rapid ring flipping results in the interconversion of the axial proton to an equatorial proton and an equatorial to the axial proton. Such interconversions are too rapid and cannot be detected on the NMR timescale. Hence, the NMR spectrometer cannot distinguish between the...
834
Photochemical Electrocyclic Reactions: Stereochemistry
1.8K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.8K
Stereoisomerism
11.9K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
11.9K
Polymer Classification: Crystallinity
2.8K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
2.8K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.3K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.3K
Hydrogen Bonds
8.4K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
8.4K


