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Nuclear magnetic resonance compounds

Present day techniques for structure determination in carbohydrate chemistry are sub stantially the same as those for any other type of compound The full range of modern instrumental methods including mass spectrometry and infrared and nuclear magnetic resonance spectroscopy is brought to bear on the problem If the unknown substance is crystalline X ray diffraction can provide precise structural information that m the best cases IS equivalent to taking a three dimensional photograph of the molecule... [Pg.1052]

Ideally, a mass spectmm contains a molecular ion, corresponding to the molecular mass of the analyte, as well as stmcturaHy significant fragment ions which allow either the direct deterrnination of stmcture or a comparison to Hbraries of spectra of known compounds. Mass spectrometry (ms) is unique in its abiUty to determine direcdy the molecular mass of a sample. Other techniques such as nuclear magnetic resonance (nmr) and infrared spectroscopy give stmctural information from which the molecular mass may be inferred (see Infrared technology and raman spectroscopy Magnetic spin resonance). [Pg.539]

Spectrometric Analysis. Remarkable developments ia mass spectrometry (ms) and nuclear magnetic resonance methods (nmr), eg, secondary ion mass spectrometry (sims), plasma desorption (pd), thermospray (tsp), two or three dimensional nmr, high resolution nmr of soHds, give useful stmcture analysis information (131). Because nmr analysis of or N-labeled amino acids enables determiaation of amino acids without isolation from organic samples, and without destroyiag the sample, amino acid metaboHsm can be dynamically analy2ed (132). Proteia metaboHsm and biosynthesis of many important metaboUtes have been studied by this method. Preparative methods for labeled compounds have been reviewed (133). [Pg.285]

Nuclear magnetic resonance (nmr) spectroscopy is useful for determining quaternary stmcture. The N-nmr can distinguish between quaternary ammonium compounds and amines, whether primary, secondary, or tertiary, as well as provide information about the molecular stmcture around the nitrogen atom. The C-nmr can distinguish among oleic, tallow, and hydrogenated tallow sources (194). [Pg.378]

An unusual method for the preparation of syndiotactic polybutadiene was reported by The Goodyear Tire Rubber Co. (43) a preformed cobalt-type catalyst prepared under anhydrous conditions was found to polymerize 1,3-butadiene in an emulsion-type recipe to give syndiotactic polybutadienes of various melting points (120—190°C). These polymers were characterized by infrared spectroscopy and nuclear magnetic resonance (44—46). Both the Ube Industries catalyst mentioned previously and the Goodyear catalyst were further modified to control the molecular weight and melting point of syndio-polybutadiene by the addition of various modifiers such as alcohols, nitriles, aldehydes, ketones, ethers, and cyano compounds. [Pg.531]

The modern electronic industry has played a very important role in the development of instrumentation based on physical-analytical methods As a result, a rapid boom in the fields of infrared, nuclear magnetic resonance (NMR), Raman, and mass spectroscopy and vapor-phase (or gas-liquid) chromatography has been observed. Instruments for these methods have become indispensable tools in the analytical treatment of fluonnated mixtures, complexes, and compounds The detailed applications of the instrumentation are covered later in this chapter. [Pg.1023]

Very little in the way of advances has occurred since 1971 in the applications of ultraviolet or infrared spectroscopy to the analysis of fluonnated organic compounds Therefore, only gas-liquid chromatography, liquid chromatography, mass spectrometry, and electron scattering for chemical analysis (ESCA) are discussed The application of nuclear magnetic resonance (NMR) spectroscopy to the analysis of fluonnated organic compounds is the subject of another section of this chapter... [Pg.1029]

Nuclear Magnetic Resonance Spectroscopy of Organofluorine Compounds... [Pg.1037]

The presence of iminium salts can be detected by chemical means or by spectroscopic methods. The chemical means of detecting iminium salts are reactions with nucleophiles and are the subject of this review. The spectroscopic methods are more useful for rapid identification because with the large number of model compounds available now the spectroscopic methods are fast and reliable. The two methods that are used primarily are infrared and nuclear magnetic resonance spectroscopy. Some attempts have been made to determine the presence of iminium salts by ultraviolet spectroscopy, but these are not definitive as yet (14,25). [Pg.176]

The pKa values of 4-hydroxypyridine 1-oxide (51 52) and the methylated derivatives of both tautomeric forms indicate that the parent compound exists as a mixture containing comparable amounts of both forms in aqueous solution. Nuclear magnetic resonance spectra support this conclusion, but the ultraviolet spectra of the tautomeric compound and both alkylated derivatives are too similar to give information concerning the structural nature of the former. ... [Pg.359]

Nuclear magnetic resonance spectra of all four parent compounds have been measured and analyzed.The powerful potentialities of NMR as a tool in the study of covalent hydration, tautomerism, or protonation have, however, as yet received no consideration for the pyridopyrimidines. NMR spectra have been used to distinguish between pyrido[3,2-d]pyrimidines. and isomeric N-bridgehead compounds such as pyrimido[l,2- ]pyrimidines and in several other structural assignments (cf. 74 and 75). [Pg.185]

Snyder and his co-workers assigned structures 48 and 49 to these j6-hydroxythiophene derivatives on the basis of chemical evidence and infrared and nuclear magnetic resonance spectral data. Infrared and nuclear magnetic resonance spectra further indicate that compounds of type 49 exist as dimers, probably hydrogen bonded, when R = OC2H5 or CH3, but as monomeric enols when R = H. ... [Pg.10]

The tautomerism of 2- and 3-aminothiophenes was mentioned by Hartough in his review of thiophenes/ but the first definite evidence became available in 1961 when Hoffman and Gronowitz showed conclusively by nuclear magnetic resonance spectroscopy that these compounds both exist in the amino form. In agreement with this finding, 3-aminothiophene generally behaves as an aromatic amine. ... [Pg.22]

Revised structures have been proposed for these compounds. The brownish-yellow acid obtained with maleic anhydride has been shown by ultraviolet, infrared, and nuclear magnetic resonance absorption measurements and oxidative degradation to have the tricyclic structure... [Pg.221]


See other pages where Nuclear magnetic resonance compounds is mentioned: [Pg.526]    [Pg.8]    [Pg.690]    [Pg.138]    [Pg.219]    [Pg.387]    [Pg.458]    [Pg.220]    [Pg.126]    [Pg.116]    [Pg.227]    [Pg.1037]    [Pg.526]    [Pg.268]    [Pg.581]    [Pg.157]    [Pg.161]    [Pg.336]    [Pg.367]    [Pg.9]    [Pg.42]    [Pg.67]    [Pg.94]    [Pg.321]    [Pg.808]    [Pg.135]    [Pg.215]   
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See also in sourсe #XX -- [ Pg.95 ]

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See also in sourсe #XX -- [ Pg.512 ]




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