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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. 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 ...

  4. 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).

  5. 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 ...

  6. Nuclear magnetic resonance spectroscopy - Wikipedia

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

    Typically 2–50 mg of a substance is required to record a decent-quality NMR spectrum. The NMR method is non-destructive, thus the substance may be recovered. To obtain high-resolution NMR spectra, solid substances are usually dissolved to make liquid solutions, although solid-state NMR spectroscopy is also possible.

  7. 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).

  8. Tetramethylsilane - Wikipedia

    en.wikipedia.org/wiki/Tetramethylsilane

    Tetramethylsilane is the accepted internal standard for calibrating chemical shift for 1 H, 13 C and 29 Si NMR spectroscopy in organic solvents (where TMS is soluble). In water, where it is not soluble, sodium salts of DSS, 2,2-dimethyl-2-silapentane-5-sulfonate, are used instead. Because of its high volatility, TMS can easily be evaporated ...

  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 ...