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相关概念视频

Halogens03:01

Halogens

18.3K
Group 17 elements, known as halogens, are nonmetals. At room temperature, fluorine and chlorine are gases, bromine is a liquid, and iodine a solid. Astatine is a highly unstable radioactive element, so currently, most of its properties are unknown due to its short half-life. Tennessine is a synthetic element also predicted to be in this group. 
18.3K
Valence Bond Theory02:45

Valence Bond Theory

31.9K
Overview of Valence Bond Theory
31.9K
Alkyl Halides02:45

Alkyl Halides

16.3K
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...
16.3K
Intermolecular Forces03:13

Intermolecular Forces

57.7K
Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen...
57.7K
Intermolecular vs Intramolecular Forces03:00

Intermolecular vs Intramolecular Forces

86.6K
Intermolecular forces (IMF) are electrostatic attractions arising from charge-charge interactions between molecules. The strength of the intermolecular force is influenced by the distance of separation between molecules. The forces significantly affect the interactions in solids and liquids, where the molecules are close together. In gases, IMFs become important only under high-pressure conditions (due to the proximity of gas molecules). Intermolecular forces dictate the physical properties of...
86.6K
Radical Halogenation: Thermodynamics01:34

Radical Halogenation: Thermodynamics

3.7K
The thermodynamic favorability of a reaction is determined by the change in Gibbs free energy (ΔG). ΔG has two components- enthalpy (ΔH) and entropy (ΔS). The entropy component is negligible for alkane halogenation because the number of reactants and product molecules are equal. In this case, the ΔG is governed only by the enthalpy component. The most crucial factor that determines ΔH is the strength of the bonds. ΔH can be determined by comparing the energy...
3.7K

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相关实验视频

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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

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调节不同原子之间的竞争以形成素键.

Steve Scheiner1

  • 1Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322-0300, United States.

The journal of physical chemistry. A
|November 11, 2024
PubMed
概括

链上的替代物可以逆转和原子之间的素结合偏好. 由于电子云的移动性,这种控制在芳香环中更具挑战性.

科学领域:

  • 计算化学是一种计算化学.
  • 超分子化学 超分子化学
  • 有机化学 有机化学

背景情况:

  • 素结合 (XB) 是一种涉及易斯基和电友素原子的非共价相互作用.
  • 素键的强度通常与素的大小和极化性相关,较大的素,如,形成比更强的键.
  • 控制素键的选择性和强度对于设计分子识别和自组装系统至关重要.

研究的目的:

  • 为了研究替代剂在链上的放置对素键供体选择性的影响.
  • 探索扭转和之间固有的素键偏好的可行性.
  • 为了比较替代剂对基链与芳香环在调节素键相互作用中的作用.

主要方法:

  • 密度函数理论 (DFT) 的计算被用来建模素结合相互作用.
  • 该研究的重点是涉及 (I) 和 (Br) 原子作为素键捐赠体和氨 (NH3) 作为核爱体的系统.
  • 系统地分析了替代剂对n-丁链和芳香环的作用.

主要成果:

  • DFT的计算显示,作为素键捐赠体对的内在偏好可以通过在n-丁链上的战略替代物放置来逆转.
  • 在与电友相互作用的替代剂中,观察到与氧 (O) 与 (N) 原子相比的氧 (O) 和 (N) 原子在供体强度的类似逆转.
  • 当竞争中的素原子是芳香系统的一部分时,扭转这些偏好被发现是显著更具挑战性的,这归因于移动的pi电子云.

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The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique

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相关实验视频

Last Updated: Jun 7, 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

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Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers

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The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique

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结论:

  • 在链上的替代工程提供了一个可行的策略来调整和逆转素键供体选择性.
  • 电子环境,特别是电子捐赠或提取组的存在,在调节素键强度和选择性方面发挥着至关重要的作用.
  • 芳香系统在实现这种逆转方面存在固有的挑战,原因是它们的电子结构未定位,影响了素结合相互作用的微调.