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  2. Proton nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Proton_nuclear_magnetic...

    Each doublet will have the same area because both doublets are produced by one proton each. The two doublets at 1 ppm and 2.5 ppm from the fictional molecule CH−CH are now changed into CH 2 −CH: The total area of the 1 ppm CH 2 peak will be twice that of the 2.5 ppm CH peak.

  3. Nuclear magnetic resonance spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Nuclear_magnetic_resonance...

    A 900 MHz NMR instrument with a 21.1 T magnet at HWB-NMR, Birmingham, UK Nuclear magnetic resonance spectroscopy, most commonly known as NMR spectroscopy or magnetic resonance spectroscopy (MRS), is a spectroscopic technique based on re-orientation of atomic nuclei with non-zero nuclear spins in an external magnetic field.

  4. Nuclear magnetic resonance spectra database - Wikipedia

    en.wikipedia.org/wiki/Nuclear_magnetic_resonance...

    The Spectral Database for Organic Compounds (SDBS) is developed and maintained by Japan's National Institute of Advanced Industrial Science and Technology. SDBS includes 14700 1 H NMR spectra and 13000 13 C NMR spectra as well as FT-IR, Raman, ESR, and MS data. The data are stored and displayed as an image of the processed data.

  5. Aromatic ring current - Wikipedia

    en.wikipedia.org/wiki/Aromatic_ring_current

    Magnetically induced probability current density vectors in benzene (C 6 H 6) calculated explicitly using quantum chemical methods. B 0 is set perpendicular to the molecular plane, in the left subfigure only vectors in the molecular plane are shown, in the right subfigure only vectors 1 a.u. (~52 pm) above the molecular plane are shown.

  6. Carbon-13 NMR satellite - Wikipedia

    en.wikipedia.org/wiki/Carbon-13_NMR_satellite

    Carbon satellites in physics and spectroscopy, are small peaks that can be seen shouldering the main peaks in the nuclear magnetic resonance (NMR) spectrum.These peaks can occur in the NMR spectrum of any NMR active atom (e.g. 19 F or 31 P NMR) where those atoms adjoin a carbon atom (and where the spectrum is not 13 C-decoupled, which is usually the case).

  7. Fluorine-19 nuclear magnetic resonance spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Fluorine-19_nuclear...

    19 F NMR chemical shifts in the literature vary strongly, commonly by over 1 ppm, even within the same solvent. [5] Although the reference compound for 19 F NMR spectroscopy, neat CFCl 3 (0 ppm), [6] has been used since the 1950s, [7] clear instructions on how to measure and deploy it in routine measurements were not present until recently. [5]

  8. Spectral Database for Organic Compounds - Wikipedia

    en.wikipedia.org/wiki/Spectral_Database_for...

    The 1 H NMR spectra were recorded at a resonance frequency of 400 MHz with a resolution of 0.0625 Hz or at 90 MHz with a resolution of 0.125 Hz. The spectral acquisition was carried out using a flip angle of 22.5 – 30.0 degrees and a pulse repetition time of 30 seconds. [ 4 ]

  9. Triple-resonance nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Triple-resonance_nuclear...

    Triple resonance experiments are a set of multi-dimensional nuclear magnetic resonance spectroscopy (NMR) experiments that link three types of atomic nuclei, most typically consisting of 1 H, 15 N and 13 C.