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Nuclear magnetic resonance spectroscopy solvents

Duthaler, R.O. and Roberts, J.D., Nitrogen-15 nuclear magnetic resonance spectroscopy solvent effects on the 15N chemical shifts of saturated amines and their hydrochlorides, J. Magn. Reson., 34, 129, 1979. [Pg.434]

Key Words Nuclear magnetic resonance spectroscopy, Solvent, Water suppression. Radiation damping. Demagnetization field. Bulk susceptibility effect. Presaturation, Watergate, Purge, Metabonomics. [Pg.34]

Instmmental methods of analysis provide information about the specific composition and purity of the amines. QuaUtative information about the identity of the product (functional groups present) and quantitative analysis (amount of various components such as nitrile, amide, acid, and deterruination of unsaturation) can be obtained by infrared analysis. Gas chromatography (gc), with a Hquid phase of either Apiezon grease or Carbowax, and high performance Hquid chromatography (hplc), using siHca columns and solvent systems such as isooctane, methyl tert-huty ether, tetrahydrofuran, and methanol, are used for quantitative analysis of fatty amine mixtures. Nuclear magnetic resonance spectroscopy (nmr), both proton ( H) and carbon-13 ( C), which can be used for quaHtative and quantitative analysis, is an important method used to analyze fatty amines (8,81). [Pg.223]

Nuclear Magnetic Resonance Spectroscopy Measured in a Chiral Solvent or with a Chiral Solvating Agent. One method of NMR analysis for enantiomer composition is to record the spectra in a chiral environment, such as a chiral solvent or a chiral solvating agent. This method is based on the diastereomeric interaction between the substrate and the chiral environment applied in the analysis. [Pg.20]

Nuclear magnetic resonance spectroscopy of dilute polymer solutions is utilized routinely for analysis of tacticlty, of copolymer sequence distribution, and of polymerization mechanisms. The dynamics of polymer motion in dilute solution has been investigated also by protoni - and by carbon-13 NMR spectroscopy. To a lesser extent the solvent dynamics in the presence of polymer has been studied.Little systematic work has been carried out on the dynamics of both solvent and polymer in the same systan. [Pg.143]

J. W. Emsley and J. C. Lindon, Nuclear Magnetic Resonance Spectroscopy Using Liquid Crystal Solvents, Pergamon Press, Oxford, 1975. [Pg.225]

Bottomley PA (1987) Spatial localization in NMR spectroscopy in vivo. Ann NY Acad Sci 508 333-348 Bottomley PA, Edelstein WA, Foster TH, Adams WA (1985) In vivo solvent-suppressed localized hydrogen nuclear magnetic resonance spectroscopy a window to metabolism Proc Natl Acad Sci USA 82 2148-2152 Brown TR, Kincaid BM, Ugurbil K (1982) NMR chemical shift imaging in three dimensions. Proc Natl Acad Sci USA 79 3523-3526... [Pg.181]

To determine the nature of the silicon moieties in a polymer, clearly the easiest method would be a technique that provides a direct observation of the silicon atom and meaningful, interpretable information on the atom. Nuclear magnetic resonance spectroscopy tuned to the Si isotope ( Si NMR) is a tool of this nature it can directly probe the state of the silicon atom, and with it one can often readily determine the extent to which Si-O-Si crosslinks (fi-om silanol condensation), have formed. One can observe spectra of silicon-containing compounds either dissolved in a solvent or in the solid state. Liquid-state Si NMR, while the most sensitive, cannot be used quantitatively on heterogeneous systems such a latex formulations. Therefore, one must separate the liquid and solid portions of the latex (without heat, which would promote hydrolysis and condensation) and use the solid residue for the Si NMR experiments. [Pg.743]


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See also in sourсe #XX -- [ Pg.6 , Pg.75 ]




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