超原子化学和组装中的形状匹配
Jingjing Yang1, Feifan Wang1, Jake C Russell1
1Department of Chemistry, Columbia University, New York, New York 10027, United States.
Journal of the American Chemical Society
|July 1, 2020
概括
研究人员使用异型超原子纳米集群创建了新的层次固体. 这些结构允许调整晶体包装和光学特性,为先进的材料设计展示了一条新途径.
科学领域:
- 材料科学
- 纳米技术
- 固态化学
背景情况:
- 超原子纳米集群为层级固体提供独特的构建块.
- 纳米集群的异型形状使得新的组装可能性成为可能.
研究的目的:
- 探索使用几何异型纳米集群创建新的超原子架构.
- 调查形状异构在固态组装和特性中的作用.
主要方法:
- 合成棒状的Co12Se16(PEt3) 10和C140纳米集群.
- 在新型超原子架构中组装异型纳米集群.
- 晶体包装的特征,空隙形成和电子性质.
主要成果:
- 发现来自异型纳米集群的新型超原子结构.
- 对容纳溶剂分子的空隙的非密闭包装结构的观察.
- 通过间隔溶剂分子调整晶体包装和光学间隙的演示.
- 对电导"开启"现象的观察.
结论:
- 无原子超原子纳米集群是层次固体的多功能构建块.
- 形状异构性和间接分子提供对固态结构和属性的控制.
- 这种方法为设计和调整先进材料的特性提供了一条新途径.
更多相关视频
06:35Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
8.4K
14:55Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
Published on: September 17, 2017
15.8K
相关概念视频
Molecular Models
43.1K
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
43.1K
Molecular Shapes
60.9K
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...
Two regions of electron density in a diatomic...
60.9K
Hybridization of Atomic Orbitals I
64.2K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
64.2K
¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons
3.9K
Protons in identical electronic environments within a molecule are chemically equivalent and have the same chemical shift. The replacement test is a useful tool to identify chemical equivalence and predict NMR spectra. A substituent replaces each of the protons being examined and the resulting molecules are compared. If the same molecule is obtained, the protons are equivalent or homotopic. Replacement of any hydrogens in ethane by chlorine yields chloroethane because all six protons are...
3.9K
¹H NMR: Complex Splitting
1.7K
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...
1.7K
¹H NMR: Interpreting Distorted and Overlapping Signals
1.4K
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...
1.4K
