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13 C NMR spectroscopy is much less sensitive (ca. by 4 orders of magnitude) to carbon than 1 H NMR spectroscopy is to hydrogen, because of the lower abundance (1.1%) of 13 C compared to 1 H (>99%), and because of a lower(0.702 vs. 2.8) nuclear magnetic moment.
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).
Available through Wiley Online Library [3] (John Wiley & Sons), SpecInfo on the Internet NMR is a collection of approximately 440,000 NMR spectra (organized as 13 C, 1 H, 19 F, 31 P, and 29 Si NMR databases). The data are accessed via the Internet using a Java interface and are stored in a server developed jointly with BASF. The software ...
NMR-active nuclei, particularly those with a spin quantum number of 1/2, are of great significance in NMR spectroscopy. Examples include 1 H, 13 C, 15 N, and 31 P. [10] Some atoms with very high spin (as 9/2 for 99 Tc atom) are also extensively studied with NMR spectroscopy. [11]
Bulk carbon-13 for commercial use, e.g. in chemical synthesis, is enriched from its natural 1% abundance. Although carbon-13 can be separated from the major carbon-12 isotope via techniques such as thermal diffusion, chemical exchange, gas diffusion, and laser and cryogenic distillation, currently only cryogenic distillation of methane (boiling point −161.5°C) or carbon monoxide (b.p. − ...
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).
Carbon satellites are small because only very few of the molecules in the sample have that carbon as the rare NMR-active 13 C isotope. As always for coupling due to a single spin-1/2 nucleus, the signal splitting for the H attached to the 13 C is a doublet. The H attached to the more abundant 12 C is not split, so it is a large singlet. The net ...
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 ]