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Template: NMR solvents. 5 languages. ... This page was last edited on 1 October 2024, at 14:21 (UTC).
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.
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 ...
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]
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 ...
For 31 P NMR, the range is hundreds of ppm. [22] In paramagnetic NMR spectroscopy, the samples are paramagnetic, i.e. they contain unpaired electrons. The paramagnetism gives rise to very diverse chemical shifts. In 1 H NMR spectroscopy, the chemical shift range can span up to thousands of ppm. [23]
Deuterated acetone ((CD 3) 2 CO), also known as acetone-d 6, is a form (isotopologue) of acetone (CH 3) 2 CO in which the hydrogen atom (H) is replaced with deuterium (heavy hydrogen) isotope (2 H or D). Deuterated acetone is a common solvent used in NMR spectroscopy. [1]
Deuterated benzene is a common solvent used in NMR spectroscopy. It is widely used for taking spectra of organometallic compounds, which often react with the cheaper deuterated chloroform. [3] A slightly more exotic application of C 6 D 6 is in the synthesis of molecules containing a deuterated phenyl group.