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  2. Carbon-13 nuclear magnetic resonance - Wikipedia

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

    Although ca. 1 mln. times less sensitive than 1 H NMR spectroscopy, 13 C NMR spectroscopy is widely used for characterizing organic and organometallic compounds, primarily because 1H-decoupled 13C-NMR spectra are more simple, have a greater sensitivity to differences in the chemical structure, and, thus, are better suited for identifying ...

  3. 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).

  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. Paramagnetic nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Paramagnetic_nuclear...

    The difference between the chemical shift of a given nucleus in a diamagnetic vs. a paramagnetic environment is called the hyperfine shift.In solution the isotropic hyperfine chemical shift for nickelocene is −255 ppm, which is the difference between the observed shift (ca. −260 ppm) and the shift observed for a diamagnetic analogue ferrocene (ca. 5 ppm).

  6. Nuclear magnetic resonance spectroscopy - Wikipedia

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

    The chemical shifts of a molecule change slightly between solvents, and therefore the solvent used is almost always reported with chemical shifts. [ citation needed ] Proton NMR spectra are often calibrated against the known solvent residual proton peak [ 16 ] as an internal standard instead of adding tetramethylsilane (TMS), which is ...

  7. 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

  8. Nuclear magnetic resonance chemical shift re-referencing

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

    In a recent study, [11] a chemical shift re-referencing program (PANAV) was run on a total of 2421 BMRB entries that had a sufficient proportion of (>80%) of assigned chemical shifts to perform a robust chemical shift reference correction. A total of 243 entries were found with 13Cα shifts offset by more than 1.0 ppm, 238 entries with 13Cβ ...

  9. Nuclear magnetic resonance decoupling - Wikipedia

    en.wikipedia.org/wiki/Nuclear_Magnetic_Resonance...

    1 H (proton) NMR spectroscopy and 13 C NMR spectroscopy analyze 1 H and 13 C nuclei, respectively, and are the most common types (most common analyte isotopes which show signals) of NMR spectroscopy. Homonuclear decoupling is when the nuclei being radio frequency (rf) irradiated are the same isotope as the nuclei being observed (analyzed) in ...