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相关概念视频

The Quantum-Mechanical Model of an Atom02:45

The Quantum-Mechanical Model of an Atom

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Shortly after de Broglie published his ideas that the electron in a hydrogen atom could be better thought of as being a circular standing wave instead of a particle moving in quantized circular orbits, Erwin Schrödinger extended de Broglie’s work by deriving what is now known as the Schrödinger equation. When Schrödinger applied his equation to hydrogen-like atoms, he was able to reproduce Bohr’s expression for the energy and, thus, the Rydberg formula governing hydrogen spectra.
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¹H NMR: Long-Range Coupling01:27

¹H NMR: Long-Range Coupling

1.8K
The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
1.8K
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)01:20

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

1.1K
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...
1.1K
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)01:22

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

1.1K
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...
1.1K
Molecular Orbital Theory I02:35

Molecular Orbital Theory I

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Overview of Molecular Orbital Theory
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Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

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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...
47.3K

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相关实验视频

Updated: Jul 20, 2025

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
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Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

Published on: April 8, 2020

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单元合星团:捕捉量子时刻

Ilias Magoulas1, Francesco A Evangelista1

  • 1Department of Chemistry and Cherry Emerson Center for Scientific Computation, Emory University, Atlanta, Georgia 30322, United States.

The journal of physical chemistry. A
|July 31, 2023
PubMed
概括

使用非代能量校正的浅量子电路加快了计算化学模拟的融合. 这种方法可以在更紧的电路中产生化学精确的能量,从而提高量子硬件的噪声弹性.

科学领域:

  • 量子计算是一种量子计算.
  • 计算化学是一种计算化学.
  • 量子算法中的量子算法

背景情况:

  • 在杂的量子硬件上进行精确的计算化学模拟,浅,CNOT高效的量子电路是必不可少的.
  • 当前的方法在有效地实现完整的配置交互方面面临着挑战.

研究的目的:

  • 在量子化学模拟中探索非代的能量校正来加速融合.
  • 评估使用紧量子电路获得化学精确能量的潜力.

主要方法:

  • 使用合集群理论的时刻方法进行非代能量校正.
  • 在量子模拟中使用代构造的命题.
  • 评估电路深度和 CNOT 门效率.

主要成果:

  • 初步结果表明,加速趋同,朝着完全的配置交互方向发展.
  • 使用更紧的电路获得了化学精确的能量.
  • 拟议的方法证明了对门和脱凝噪声的增强弹性.

结论:

  • 非代的能量校正为高效的量子化学模拟提供了一个有希望的途径.
  • 从这种方法获得的紧量子电路提高了对当前杂硬件进行准确模拟的可行性.

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