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  2. Deuterium NMR - Wikipedia

    en.wikipedia.org/wiki/Deuterium_NMR

    Deuterium is an isotope with spin = 1, unlike hydrogen-1, which has spin = 1/2. The term deuteron NMR, in direct analogy to proton NMR, is also used. [ 2 ] Deuterium NMR has a range of chemical shift similar to proton NMR but with poor resolution, due to the smaller magnitude of the magnetic dipole moment of the deuteron relative to the proton.

  3. Deuterated solvent - Wikipedia

    en.wikipedia.org/wiki/Deuterated_solvent

    Deuterated chloroform. Deuterated solvents are a group of compounds where one or more hydrogen atoms are substituted by deuterium atoms. These isotopologues of common solvents are often used in nuclear magnetic resonance spectroscopy. [1]

  4. Deuterated DMSO - Wikipedia

    en.wikipedia.org/wiki/Deuterated_DMSO

    13 C NMR Spectrum of DMSO-d 6. Pure deuterated DMSO shows no peaks in 1 H NMR spectroscopy and as a result is commonly used as an NMR solvent. [2] However commercially available samples are not 100% pure and a residual DMSO-d 5 1 H NMR signal is observed at 2.50ppm (quintet, J HD =1.9Hz). The 13 C chemical shift of DMSO-d 6 is 39.52ppm (septet ...

  5. Proton nuclear magnetic resonance - Wikipedia

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

    Occasionally, small peaks can be seen shouldering the main 1 H NMR peaks. These peaks are not the result of proton-proton coupling, but result from the coupling of 1 H atoms to an adjoining carbon-13 (13 C) atom. These small peaks are known as carbon satellites as they are small and appear around the main 1 H peak i.e. satellite (around) to

  6. Deuterated chloroform - Wikipedia

    en.wikipedia.org/wiki/Deuterated_chloroform

    Commercial chloroform-d does, however, still contain a small amount (0.2% or less) of non-deuterated chloroform; this results in a small singlet at 7.26 ppm, known as the residual solvent peak, which is frequently used as an internal chemical shift reference. In carbon-13 NMR spectroscopy, the sole carbon in deuterated chloroform shows a ...

  7. Nuclear magnetic resonance spectroscopy - Wikipedia

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

    This paramagnetic contribution, which is unrelated to paramagnetism) not only disrupts trends in chemical shifts, which complicates assignments, but it also gives rise to very large chemical shift ranges. For example, most 1 H NMR signals for most organic compounds are within 15 ppm. For 31 P NMR, the range is hundreds of ppm. [22]

  8. Template:NMR solvents - Wikipedia

    en.wikipedia.org/wiki/Template:NMR_solvents

    Template: NMR solvents. 5 languages. ... This page was last edited on 1 October 2024, at 14:21 (UTC).

  9. Deuterated methanol - Wikipedia

    en.wikipedia.org/wiki/Deuterated_methanol

    Deuterated methanol (CD 3 OD), is a form (called an isotopologue) of methanol (CH 3 OH) in which the hydrogen atoms ("H") are replaced with deuterium (heavy hydrogen) isotope ("D"). [1] Deuterated methanol is a common solvent used in NMR spectroscopy .