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相关概念视频

¹H NMR of Conformationally Flexible Molecules: Temporal Resolution00:52

¹H NMR of Conformationally Flexible Molecules: Temporal Resolution

At room temperature, the chair conformer of cyclohexane undergoes rapid ring flipping between two equivalent chair conformers at a rate of approximately 105 times per second. These two chair conformers are in equilibrium. The rapid ring flipping results in the interconversion of the axial proton to an equatorial proton and an equatorial to the axial proton. Such interconversions are too rapid and cannot be detected on the NMR timescale. Hence, the NMR spectrometer cannot distinguish between the...
Spin–Spin Coupling: One-Bond Coupling01:17

Spin–Spin Coupling: One-Bond Coupling

Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)01:22

Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)

Vicinal or three-bond coupling is commonly observed between protons attached to adjacent carbons. Here, nuclear spin information is primarily transferred via electron spin interactions between adjacent C‑H bond orbitals. This generally favors the antiparallel arrangement of spins, so 3J values are usually positive.
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
P-N junction01:11

P-N junction

A p-n junction is formed when p-type and n-type semiconductor materials are joined together. At the interface of the p-n junction, holes from the p-side and electrons from the n-side begin to diffuse into the opposite sides due to the concentration gradient. This diffusion of carriers leads to a region around the junction where there are no free charge carriers, known as the depletion region. The charge density within the depletion region for the n-side and p-side can be described by the...
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)01:20

Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)

Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
Metal-Semiconductor Junctions01:24

Metal-Semiconductor Junctions

The contact of metal and semiconductor can lead to the formation of a junction with either Schottky or Ohmic behavior.
Schottky Barriers
Schottky barriers arise when a metal with a work function (Φm) contacts a semiconductor with a different work function (Φs). Initially, electrons transfer until the Fermi levels of the metal and semiconductor align at equilibrium. For instance, if Φm > Φs, the semiconductor Fermi level is higher than the metal's before contact. The semiconductor's...

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Single-Molecule Förster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1
11:27

Single-Molecule Förster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1

Published on: September 18, 2019

在单分子连接处的挫折旋转.

Young S Park1, Jonathan R Widawsky, Maria Kamenetska

  • 1Department of Chemistry, Columbia University, New York, New York, USA.

Journal of the American Chemical Society
|September 3, 2009
PubMed
概括
此摘要是机器生成的。

黄金-素键的分子定位会影响结合分子中的电子运输. 黄金电极,石化单双和芳香PI系统之间更大的重叠增强了分子连接导电性.

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科学领域:

  • 分子电子学分子电子学
  • 有机化学 有机化学
  • 表面科学是一门科学.

背景情况:

  • 了解分子连接处的电荷传输对于开发新型电子设备至关重要.
  • 电极和有机分子之间的接口显著影响设备性能.

研究的目的:

  • 为了研究金-素键的方向如何影响通过结合分子的电子运输.
  • 阐明素单双和芳香PI系统在分子导电性中的作用.

主要方法:

  • 专门设计的分子连接点的导电性测量.
  • 不同分子架构之间的导电性比较 (例如1,4-bis(methylthio) 与四二二甲).

主要成果:

  • 黄金-硫 (Au-S) 和黄金- (Au-Se) 键相对于芳香PI系统的方向明确控制电子传输.
  • 导电通道涉及单双的石灰电极,将黄金电极连接到芳香PI系统.
  • 这些组件之间越来越多的重叠导致更高的导电率.

结论:

  • 在电极-分子接口的分子方向是控制电荷传输的关键因素.
  • 素与芳香系统的单对相互作用对于分子连接处的高效电子运输至关重要.
  • 这项工作为设计高性能分子电子设备提供了基本的见解.