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相关概念视频

Ionic Bonding and Electron Transfer02:48

Ionic Bonding and Electron Transfer

41.3K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions. 
41.3K
Alkyl Halides02:45

Alkyl Halides

16.4K
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
16.4K
Mass Spectrometry: Alkyl Halide Fragmentation01:22

Mass Spectrometry: Alkyl Halide Fragmentation

1.0K
Chlorine isotopes exist as 35Cl and 37Cl in a 3:1 ratio, while bromine isotopes exist as 79Br and 81Br in a 1:1 ratio. The mass spectrum of alkyl halides typically produces two distinct molecular ion peaks, the molecular ion peak, [M], and the molecular ion plus two, [M + 2] peak. The relative heights of these two peaks are proportional to the isotopic abundance ratios of the halide. For example, 2‐chloropropane and 1‐bromopropane display two peaks with relative peak heights in a 3:1 and...
1.0K
Trends in Lattice Energy: Ion Size and Charge02:54

Trends in Lattice Energy: Ion Size and Charge

23.8K
An ionic compound is stable because of the electrostatic attraction between its positive and negative ions. The lattice energy of a compound is a measure of the strength of this attraction. The lattice energy (ΔHlattice) of an ionic compound is defined as the energy required to separate one mole of the solid into its component gaseous ions. For the ionic solid sodium chloride, the lattice energy is the enthalpy change of the process:
23.8K
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

41.8K
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,...
41.8K
Ionic Crystal Structures02:42

Ionic Crystal Structures

14.2K
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
14.2K

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相关实验视频

Updated: Jun 17, 2025

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

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内离子激发状态化物化物灭的周期性趋势

Matthew J Goodwin1, Alexander M Deetz1, Paul J Griffin1

  • 1Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

Inorganic chemistry
|August 9, 2024
PubMed
概括

非共价相互作用稳定了反应物,显著影响了光启动的电子转移. 一种新的光催化剂显示了化物反应性趋势,受化物大小和电子亲和力的影响.

科学领域:

  • 摄影化学的使用.
  • 无机化学 无机化学
  • 物理化学 物理化学

背景情况:

  • 非共价相互作用影响光启动的氧化还原反应中的激发状态反应性.
  • 相关物种的稳定影响光启动电子转移的动力学和热力学.

研究的目的:

  • 为了研究一种新型的(III) 光催化剂与化物 (化物,化物,化物) 的反应性.
  • 探索非共价相互作用对光反行为和电子转移动态的影响.

主要方法:

  • 合成一种(III) 光催化剂与一种对阴离子敏感的,用胺替代的双二连接物.
  • 研究光催化剂与化物在乙二 (极性) 和二甲 (非极性) 溶剂中的反应性.
  • 结合关系的分析,火机制 (静态和动态) 和光物理性质.

主要成果:

  • 观察到化物结合亲和度的周期性趋势,随着离子半径的减少 (Keq从~10^3到>10^6) 在极地介质中增加.
  • 在非极性介质中的所有化物中观察到固体测量相关性.
  • 对于化物和化物,静态火是显而易见的,而对于所有化物,则发生动态火.

结论:

  • quenchers 通过键的预关联显著影响化物 adduct 光物理.

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  • 内离子光氧化的热力学是由非共价相互作用调节的.
  • 化物大小和电子亲和力是决定光反反应行为的关键因素.