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Magnetic resonance spectroscopy absorption

The reaction can be followed by proton magnetic resonance spectroscopy. The original absorption for the vinyl proton disappears and two new absorption peaks appear, one in the vinyl region (ca. <5 6.5, chloroform-d) and the other in the methine region of the spectrum. There are two products formed, presumably the cis- and tfraws-isomers, in the ratio of 95 5, respectively. The checkers also obtained the same yield when the reaction quantities were doubled. [Pg.35]

The progress of the reaction is followed by proton magnetic resonance spectroscopy. When the absorption for the vinyl proton (ca. <5 6.6, chloroform-d) is completely absent, the reaction is stopped. Several minor products that were not identified are also formed in this step. [Pg.36]

Supercritical fluid chromatography Thin-layer chromatography Atomic absorption spectroscopy Nuclear magnetic resonance spectroscopy Mass spectrometry Fourier transform infrared spectrometry... [Pg.84]

Atomic Absorption and Emission Spectroscopy Nuclear Magnetic Resonance Spectroscopy X-ray Methods Mass Spectrometry... [Pg.247]

There are two major experimental techniques that can be used to analyze hydrogen bonding in noncrystalline polymer systems. The first is based on thermodynamic measurements which can be related to molecular properties by using statistical mechanics. The second, and much more powerful, way to elucidate the presence and nature of hydrogen bonds in amorphous polymers is by using spectroscopy (Coleman et al., 1991). From the present repertoire of spectroscopic techniques which includes IR, Raman, electronic absorption, fluorescence, and magnetic resonance spectroscopy, the IR is by far the most sensitive to the presence of hydrogen bonds (Coleman et al., 1991). [Pg.97]

Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy ( ll NMR) have become standards for verifying the chemistry of polyanhydrides. The reader is referred to the synthesis literature in the previous section for spectra of specific polymers. The FTIR spectrum for PSA is shown in Fig. 2. In FTIR the absorption... [Pg.189]

The determination of the various types of geometric isomers associated with unsaturation in Polymer chains is of great importance, for example, in the study of the structure of modern synthetic rubbers. In table below are listed some of the important infrared absorption bands which arise from olefinic groups. In synthetic "natural" rubber, cis-1, 4-polyisoprene, relatively small amounts of 1, 2 and 3, 4-addition can easily be detected, though it is more difficult to distinguish between the cis and trans-configurations. Nuclear magnetic resonance spectroscopy is also useful for this analysis. [Pg.79]

A reevaluation of molecular structure of humic substances based on data obtained primarily from nuclear magnetic resonance spectroscopy, X-ray absorption near-edge structure spectroscopy, electrospray ionization-mass spectrometry, and pyrolysis studies was presented by Sutton and Sposito (2005). The authors consider that humic substances are collections of diverse, relatively low molecular mass components forming dynamic associations stabilized by hydrophobic interactions and hydrogen bonds. These associations are capable of organizing into micellar structures in suitable aqueous environments. Humic components display contrasting molecular motional behavior and may be spatially segregated on a scale of nanometers. Within this new structural context, these components comprise any molecules... [Pg.16]

Nuclear magnetic resonance spectroscopy is a form of absorption spectroscopy and concerns radio frequency (rf)-induced transitions between quantized energy states of nuclei that have been oriented by magnetic fields. Several nonmathemati-cal introductions to NMR are recommended to supplement the material here [1-9]. For greater mathematical depth, a number of excellent texts are available [10-26]. [Pg.83]

Fourier transform methods have revolutionized many fields in physics and chemistry, and applications of the technique are to be found in such diverse areas as radio astronomy [52], nuclear magnetic resonance spectroscopy [53], mass spectroscopy [54], and optical absorption/emission spectroscopy from the far-infrared to the ultraviolet [55-57]. These applications are reviewed in several excellent sources [1, 54,58], and this section simply aims to describe the fundamental principles of FTIR spectroscopy. A more theoretical development of Fourier transform techniques is given in several texts [59-61], and the interested reader is referred to these for details. [Pg.5]

The techniques considered in this chapter are infrared spectroscopy (or vibrational spectroscopy), nuclear magnetic resonance spectroscopy, ultraviolet-visible spectroscopy (or electronic spectroscopy) and mass spectrometry. Absorption of infrared radiation is associated with the energy differences between vibrational states of molecules nuclear magnetic resonance absorption is associated with changes in the orientation of atomic nuclei in an applied magnetic field absorption of ultraviolet and visible radiation is associated with changes in the energy states of the valence electrons of molecules and mass spectrometry is concerned... [Pg.254]

XRF = X-ray fluorescence spectroscopy, XPS = X-ray photoelectron spectroscopy, AES = Auger electron spectroscopy, XANES = X-ray absorption near edge spectroscopy, RAIR = Reflectance-absorbance infrared spectroscopy, EXAFS = X-ray absorption fine-structure spectroscopy, ECR = Electric contact resistance, NMR = Nuclear magnetic resonance spectroscopy, IPS = Imaging photoelectron spectromicroscopy. [Pg.125]


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