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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. Nuclear magnetic resonance spectroscopy - Wikipedia

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

    The types of NMR usually done with nucleic acids are 1 H or proton NMR, 13 C NMR, 15 N NMR, and 31 P NMR. Two-dimensional NMR methods are almost always used, such as correlation spectroscopy (COSY) and total coherence transfer spectroscopy (TOCSY) to detect through-bond nuclear couplings, and nuclear Overhauser effect spectroscopy (NOESY) to ...

  5. In vivo magnetic resonance spectroscopy - Wikipedia

    en.wikipedia.org/wiki/In_vivo_magnetic_resonance...

    13 Carbon Magnetic Resonance Spectroscopy. In contrast to phosphorus NMR, carbon NMR is an insensitive technique. This arises from the fact that 13 C NMR has a low abundance (1.1%) and carbon's low gyromagnetic ratio. [19]: 93–96 This low abundance is because 12 C does not have a magnetic moment, making it not NMR active, leading to 13 C's ...

  6. Nuclear magnetic resonance decoupling - Wikipedia

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

    Since the percentage of 13 C is so low in natural isotopic abundance samples, the 13 C coupling effects on other carbons and on 1 H are usually negligible, and for all practical purposes splitting of 1 H signals due to coupling with natural isotopic abundance carbon does not show up in 1 H NMR spectra. In real life, however, the 13 C coupling ...

  7. Nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Nuclear_magnetic_resonance

    is an example of a nuclide that produces no NMR signal, whereas 13 C, 31 P, 35 Cl and 37 Cl are nuclides that do exhibit NMR spectra. The last two nuclei have spin S > ⁠ 1 / 2 ⁠ and are therefore quadrupolar nuclei. Electron spin resonance (ESR) is a related technique in which transitions between electronic rather than nuclear spin levels ...

  8. 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).

  9. Spectral Database for Organic Compounds - Wikipedia

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

    The 13 C NMR spectra were recorded at several spectrometers with resonance frequencies ranging from 15 MHz to 100 MHz and a resolution ranging from 0.025 to 0.045 ppm. Spectra were acquired using a pulse flip angle of 22.5 – 45 degrees and a pulse repetition time of 4 – 7 seconds. [4]