相关实验视频
Updated: Mar 10, 2026

06:15
Interactive Molecular Model Assembly with 3D Printing
Published on: August 13, 2020
11.1K
灵活的线性链作为阻隔器来抑制分子旋转器的内部旋转
Chengyuan Yu1, Lishuang Ma1, Jiaojiao He1
1Key Laboratory of Theoretical and Computational Photochemistry and Key Laboratory of Radiopharmaceuticals, Ministry of Education; College of Chemistry, Beijing Normal University , Beijing 100875, China.
Journal of the American Chemical Society
|December 15, 2016
概括
分子装置中的灵活链可以控制分子运动. 分子旋转上的长替代剂作为阻隔器,在高速时抑制旋转,但在低速时允许旋转,从而实现新的分子机器功能.
科学领域:
- 分子机器
- 超分子化学
- 纳米技术
背景情况:
- 人工分子装置中的灵活链通常对分子运动的控制有限.
- 了解分子组件的动力学对于设计先进的分子机器至关重要.
研究的目的:
- 用灵活的替代物研究分子旋转的动态特性.
- 在分子器件中的柔性链中建立硬体阻碍和运动速度之间的相关性.
主要方法:
- 具有刚性框架和旋器的分子旋转器的合成.
- 加入不同长度的线性醇基替代剂.
- 在NMR时间尺度上使用核磁共振 (NMR) 光谱分析动态特性.
主要成果:
- 灵活的替代剂作为弹性阻隔器,有效地抑制旋转器在中速到快速的运动.
- 在较慢的旋转速度下,替代物放松,允许完全通过旋转腔.
- 在灵活的链条中发现了固体阻碍与运动速度之间的相关性.
结论:
- 灵活的线性链可以设计为控制人造设备中的分子运动.
- 替代物的动态行为取决于分子旋转器的速度.
- 这项工作为开发具有复杂动态控制和功能的分子机器提供了基础.
相关概念视频
Conformations of Cyclohexane
16.7K
Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
16.7K
Chair Conformation of Cyclohexane
20.4K
The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of cyclohexane’s bond angle being very close to the ideal tetrahedral bond angle of 109.5° in its chair conformer. Similarly, the torsional strain is also absent owing to the perfectly staggered arrangement of bonds.
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
20.4K
Radical Chain-Growth Polymerization: Overview
3.6K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
3.6K
Conformations of Ethane and Propane
18.7K
In an organic molecule, free rotation about the carbon-carbon single bond results in energetically different conformers of the molecule. Due to this rotation, called the internal rotation, ethane has two major conformations — staggered and eclipsed.
Staggered conformation is a low energy and more stable conformation with the C-H bonds on the front carbon placed at 60°dihedral angles relative to the C-H bonds on the back carbon, leading to a reduced torsional strain. In staggered...
Staggered conformation is a low energy and more stable conformation with the C-H bonds on the front carbon placed at 60°dihedral angles relative to the C-H bonds on the back carbon, leading to a reduced torsional strain. In staggered...
18.7K
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
1.4K
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...
1.4K
Newman Projections
23.1K
Different notations are used to represent the three-dimensional structure of molecules on two-dimensional surfaces. One of the most commonly used representations is the dash-wedge formula. The dashed wedges, solid wedges, and the plane lines indicate the groups situated behind the plane, coming out of the plane, and in the plane, respectively.
The organic molecules rotate across the single bonds leading to numerous temporary three-dimensional structures of varying energy known as...
The organic molecules rotate across the single bonds leading to numerous temporary three-dimensional structures of varying energy known as...
23.1K

