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Deuterated chloroform, also known as chloroform-d, is the organic compound with the formula CDCl 3. Deuterated chloroform is a common solvent used in NMR spectroscopy. [2] The properties of CDCl 3 and ordinary CHCl 3 are virtually identical. Deuterochloroform was first made in 1935 during the years of research on deuterium. [3]
Deuterated (deuterium = 2 H, often symbolized as D) solvents especially for use in NMR are preferred, e.g. deuterated water, D 2 O, deuterated acetone, (CD 3) 2 CO, deuterated methanol, CD 3 OD, deuterated dimethyl sulfoxide, (CD 3) 2 SO, and deuterated chloroform, CDCl 3.
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]
A 900 MHz NMR instrument with a 21.1 T magnet at HWB-NMR, Birmingham, UK. Nuclear magnetic resonance spectroscopy, most commonly known as NMR spectroscopy or magnetic resonance spectroscopy (MRS), is a spectroscopic technique based on re-orientation of atomic nuclei with non-zero nuclear spins in an external magnetic field.
Samples were prepared by dissolution in deuterated chloroform (CDCl 3), deuterium oxide (D 2 O), or deuterated dimethylsulfoxide (DMSO-d 6). [5] Each spectrum is accompanied by a list of peaks with their respective intensities and chemical shifts reported in ppm and in Hz. Most spectra show the peak assignment.
Deuterated chloroform is an isotopologue of chloroform with a single deuterium atom. CDCl 3 is a common solvent used in NMR spectroscopy. Deuterochloroform is produced by the reaction of hexachloroacetone with heavy water. [31] The haloform process is now obsolete for production of ordinary chloroform.
An NMR tube filled with a colorless sample, sealed with a green polyethylene cap and Parafilm. An NMR tube is a thin glass walled tube used to contain samples in nuclear magnetic resonance spectroscopy. Typically NMR tubes come in 5 mm diameters but 10 mm and 3 mm samples are known.
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. It may be used to verify the effectiveness of deuteration: a deuterated compound will show a strong peak in 2 H NMR but not proton NMR.