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相关概念视频

Network Covalent Solids02:18

Network Covalent Solids

16.0K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
16.0K
Conformations of Cyclohexane02:11

Conformations of Cyclohexane

15.1K
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...
15.1K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

30.5K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
30.5K
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

48.0K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
48.0K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.9K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.9K
Molecular Shapes01:18

Molecular Shapes

61.1K
Molecules have characteristic shapes that are crucial for their function. The arrangement of various electron groups around the central atom dictates their molecular geometry. Electron pairs in the valence shell of a central atom will adopt an arrangement that minimizes repulsions between the electron pairs by maximizing the distance between them. The valence electrons form either bonding pairs, located primarily between bonded atoms, or lone pairs.
Two regions of electron density in a diatomic...
61.1K

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相关实验视频

Updated: Jan 8, 2026

Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
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Microfluidic-based Synthesis of Covalent Organic Frameworks COFs: A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface

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为什么共价有机框架在石墨上变得扭曲.

Veniero Lenzi1, Karol Strutyński1, Manuel Melle-Franco2

  • 1CICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, Aveiro, Portugal.

Nature communications
|December 13, 2025
PubMed
概括

研究人员研究了二酸 (PDBA) 在石墨上的共价有机框架 (COF) 的生长. 他们发现,生长条件将COF锁定在特定的扭曲堆叠中,这对于创建新型2D材料至关重要.

科学领域:

  • 材料科学 材料科学 材料科学
  • 两维材料是二维材料.
  • 超分子化学 超分子化学

背景情况:

  • 范德瓦尔斯的二维材料,包括石墨烯和共价有机框架 (COF),对超导和双电子设备具有前景.
  • 最近的进展使得石墨上高品质的二酸 (PDBA) COF 成为可能,在石墨上呈现出可重复的扭曲堆叠和moiré超级格子.

研究的目的:

  • 了解在石墨表面上形成扭曲的PDBA COFs的基本过程.
  • 调查扭转角度和增长动态在COF自组装中的作用.

主要方法:

  • 利用混合分子力学力场,以接近密度的功能理论 (DFT) 准确度.
  • 在石墨基板上模拟了PDBA COF在各种扭曲角度的生长.

主要成果:

  • 在PDBA COF生长过程中,可用的热力学最小值的数量显著减少,将结构锁定在特定的扭曲堆叠中.
  • COF前体的表面流动性高度依赖于生长结构的尺寸和扭曲角度.

结论:

  • 观察到的锁定机制和改变的表面流动性是成功合成扭曲PDBACOF单层的关键因素.
  • 这些发现为合理设计和合成具有定制电子特性的先进二维材料提供了基本的见解.

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