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Liquid Chromatography NMR

LC is the abbreviated form of the acronym HPLC (high-performance liquid chromaiography  [Pg.111]

Nuclei with / 0 can adopt certain allowed orientations in an [Pg.112]

Nuclei in molecules are affected by the local electron density and their chemical shift, the ratio of the frequency at which an NMR transition occurs to the strength of the main field as measured by the frequency at which protons resonate, is given by  [Pg.112]

Peak splitting patterns indicate the number of spin active / 0) [Pg.113]

V spectra give one line for each magnetically distinct carbon [Pg.113]


Commercially available poiybrominated aromatic ethers have been analyzed by reversed phase high performance liquid chromatography. NMR spectra of material isolated by preparative methods served to identify the observed peaks as congeners of tetrabromo to nonabromo diphenyl ether. A bromination pathway was clearly indicated. [Pg.399]

Abbreviations DMF, A,A-dimethylformamide DMA, N,A-dimethylacetamide GC, gas chromatography HPLC, high-performance liquid chromatography NMR, nuclear magnetic resonance RCM, ring closing metathesis TFA, trifluoroacetic acid THF, tetrahydrofuran. [Pg.132]

Holt, R. M. Newman, M. J. Pullen, F. S. Richards, D. S. Swanson, A. G. 1997. High-performance liquid chromatography/NMR spectrome-try/mass spectrometry further advances in hyphenated technology. J. [Pg.216]

FID = flame ionization detector GC = gas chromatography HPLC = high performance liquid chromatography NMR = nuclear magnetic resonance NS = not stated NSD = nitrogen specific detector TMS = tetramethylsi 1ane UV = ultraviolet. [Pg.102]

The molecular structure of thiophene has also been determined by liquid crystal LC (liquid chromatography) NMR spectroscopy <1984MP779, 1988MCL267> as well as ED and rotational spectroscopy. [Pg.649]

K. E. Zhang, B. Hee, C. A. Lee, B. Liang, and B. C. M. Potts, Liquid chromatography-mass spectrometry and liquid chromatography-NMR characterization of in vitro metabolites of a potent and irreversible peptidomimetic inhibitor of rhinovirus 3C protease. Drug Metab. Dispos. 29 (2001), 729-734. [Pg.933]

Czerwenka, C., Zhang, M. M., Kaehlig, H., Maier, N. M., Lipkowitz, K. B., Lindner,W. Chiral Recognition of Peptide Enantiomers by Cinchona Alkaloid Derived Chiral Selectors Mechanistic Investigations by Liquid Chromatography, NMR Spectroscopy, and Molecular Modeling, J. Org. Chem., 2003, 68, 8315-8327. [Pg.258]

Holt, R.M. Newman, M.J. Pullen, F.S. Richards, D.S. Swanson, A.G., High-Performance Liquid Chromatography/NMR Spectrometry/Mass Spectrometry Further Advances in Hyphenated Technology, J. Mass Spectrom. 32(1), 64-70 (1997). [Pg.186]

GMP 5 - guanosine monophosphate, 5 - CMP 5 - cytosine monophosphate. HPLC high - pressure liquid chromatography NMR nuclear magnetic resonance, s = singlet, d doublet, t triplet, q = quartet, m multiplet, NOE nuclear Overhauser effect, CD circular dichroism. tn trimethylene diamine, dien diethylene-triamine. CPK models Corey - Pauling - Koltun atomic models. [Pg.143]

Abbreviations BChl - bacteriochlorophyll CD - circular dichroism, EPR - electron paramagnetic resonance HPLC -high performance liquid chromatography NMR - nuclear magnetic resonance P-870 - primary donor RC - reaction center... [Pg.236]

C. Alvarez-Lorenzo, R. A. Lorenzo-Ferreira, J. L. Gomez-Amoza, R. Martinez-Pacheco, C. Souto, and A. Concheiro, A comparison of gas-liquid chromatography, NMR spectroscopy and Raman spectroscopy for determination of the substituent content of general nonionic cellulose ethers, J. Pharmaceut. Biomed. Anal, 20 (1999) 373-383. [Pg.185]


See other pages where Liquid Chromatography NMR is mentioned: [Pg.328]    [Pg.60]    [Pg.37]    [Pg.50]    [Pg.111]    [Pg.20]    [Pg.6556]    [Pg.132]    [Pg.109]    [Pg.134]    [Pg.6555]    [Pg.5]    [Pg.67]    [Pg.2658]    [Pg.2659]    [Pg.2660]    [Pg.2661]   


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