相关实验视频
Updated: May 29, 2025

10:37
Spatial Separation of Molecular Conformers and Clusters
Published on: January 9, 2014
8.9K
阶段分离非相互极性活性混合物的动态结构
Kim L Kreienkamp1, Sabine H L Klapp1
1Technische Universität Berlin, Institut für Theoretische Physik, Hardenbergstraße 36, D-10623 Berlin, Germany.
Physical review. E
|February 7, 2025
概括
在活性粒子系统中,非相互对齐会产生多样化的动态相. 显微镜模拟揭示了诸如追逐和逃跑等行为,这些行为被连续理论所遗漏,突出了需要详细的粒子级分析的需要.
科学领域:
- 物理 物理学 物理
- 软物质物理学 软物质物理学
- 活动物质物理学 活动物质物理学
背景情况:
- 非互惠的系统表现出复杂的动态,受非互惠的性质和程度的影响.
- 在不同的理论框架中理解这些动态对于预测系统行为至关重要.
研究的目的:
- 理论上研究与排斥的非相互对齐的极性活性粒子混合物的动态结构.
- 将连续模型的预测与微观粒子模拟进行比较.
主要方法:
- 连续模型的线性稳定性分析.
- 有或没有排斥性相互作用的活性极粒子的粒子模拟.
主要成果:
- 连续模型预测相位分离,集群,反集群和不对称的集群.
- 微观模拟证实了这些阶段,并揭示了像方向相关性这样的微观特性.
- 仅仅非互惠的对齐就会导致不对称的块形成,而不会产生排斥.
- 微观模拟捕捉了连续理论遗漏的"追赶和逃跑"动态.
结论:
- 非互惠性对活性物质系统中的动态阶段产生深远的影响.
- 显微镜模拟对于完全理解非互惠活性物质动态是必不可少的,它补充了连续理论.
相关概念视频
¹H NMR: Complex Splitting
1.2K
A proton M that is coupled to a proton X results in doublet signals for M. However, NMR-active nuclei can be simultaneously coupled to more than one nonequivalent nucleus. When M is coupled to a second proton A, such as in styrene oxide, each peak in the doublet is split into another doublet.
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...
1.2K
Potential Due to a Polarized Object
358
A neutral atom consists of a positively charged nucleus surrounded by a negatively charged electron cloud. When placed in an external electric field, the external electric force pulls the electrons and nucleus apart, opposite to the intrinsic attraction between the nucleus and the electrons. The opposing forces balance each other with a slight shift between the center of masses of the nucleus and the electron cloud, resulting in a polarized atom. On the other hand, a few molecules, like water,...
358
Analyte Adsorption and Distribution
593
In certain chromatographic separations, solutes transfer between the mobile phase and the stationary phase via sorption, which typically refers to the process of adsorption. For many chromatographic systems, the sorption process often depends on the polarity of the compounds—an expression of the overall dipole moment within the molecule. During the separation process, there is competition between the solute and solvent for adsorption to the stationary phase. Highly polar compounds and...
593
¹H NMR: Interpreting Distorted and Overlapping Signals
998
Spin systems where the difference in chemical shifts of the coupled nuclei is greater than ten times J are called first-order spin systems. These nuclei are weakly coupled, and their chemical shifts and coupling constant can generally be estimated from the well-separated signals in the spectrum.
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are...
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are...
998
Molecular Shape and Polarity
59.6K
Dipole Moment of a Molecule
59.6K
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
1.0K
When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
1.0K

