Related Experiment Video

Updated: Mar 18, 2026

Generation and Coherent Control of Pulsed Quantum Frequency Combs
06:42

Generation and Coherent Control of Pulsed Quantum Frequency Combs

Published on: June 8, 2018

9.8K

Determination of nonlinear nanomechanical resonator-qubit coupling coefficient in a hybrid quantum system

Qi Geng, Ka-Di Zhu

    Applied Optics
    |July 14, 2016
    PubMed

    More Related Videos

    Fabrication and Characterization of Superconducting Resonators10:26

    Fabrication and Characterization of Superconducting Resonators

    Published on: May 21, 2016

    12.0K
    Fabrication and Characterization of High-Q Silicon Nitride Membrane Resonators09:46

    Fabrication and Characterization of High-Q Silicon Nitride Membrane Resonators

    Published on: August 8, 2025

    1.3K

    Related Concept Videos

    Spin–Spin Coupling Constant: Overview01:08

    Spin–Spin Coupling Constant: Overview

    In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
    Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
    1.6K
    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...
    1.6K
    ¹H NMR: Long-Range Coupling01:27

    ¹H NMR: Long-Range Coupling

    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...
    2.9K
    NMR Spectroscopy: Spin–Spin Coupling01:08

    NMR Spectroscopy: Spin–Spin Coupling

    The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved...
    3.6K
    ¹H NMR: Interpreting Distorted and Overlapping Signals01:02

    ¹H NMR: Interpreting Distorted and Overlapping Signals

    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...
    1.7K
    Debye–Huckel–Onsager Conductance Equation01:28

    Debye–Huckel–Onsager Conductance Equation

    The Debye-Hückel-Onsager equation is a cornerstone of physical chemistry, providing a method to determine the molar conductance (Λm) and molar conductance at infinite dilution (Λ°m) for uni-univalent electrolytes.Uni-univalent electrolytes are electrolytes that dissociate in solution to produce one cation with a +1 charge and one anion with a –1 charge per formula unit.This equation addresses two crucial phenomena: the asymmetry effect and the electrophoretic effect.
    80