Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fluorine natural abundance

Although continuous wave NMR is sufficient for naturally abundant nuclei with strong magnetic moments such as hydrogen, fluorine and phosphorous, the study of low abundance nuclei and/or weak magnetic moments such as carbon 13 or silicon 29 requires pulse NMR. [Pg.65]

The upper part of the figure illustrates why the small difference in mass between an ion and its neutral molecule is ignored for the purposes of mass spectrometry. In mass measurement, has been assigned arbitrarily to have a mass of 12.00000, All other atomic masses are referred to this standard. In the lower part of the figure, there is a small selection of elements with their naturally occurring isotopes and their natural abundances. At one extreme, xenon has nine naturally occurring isotopes, whereas, at the other, some elements such as fluorine have only one. [Pg.338]

Fluorine-19, like phosphorus-31, is a spin-Vi nucleus with 100% natural abundance. The signals it produces are almost as strong as those of the proton, and the resonance frequency at a given field is also relatively close to that of the proton. Although for many years it was in fact necessary to have a special probehead for fluorine-19, those days have gone and fluorine has become a completely normal nucleus. [Pg.62]

Fluorine usually makes its presence felt in a fairly spectacular fashion, when it is present in a molecule. Once again, I = 1/2, so we only have two allowed states to worry about. Unlike 13C however, fluorine has only one isotope, 19F, and as this of course, has 100 % natural abundance, we see the whole proton signal split, instead of a couple of tiny satellites on either side of our signals ... [Pg.84]

Finally, as tabulated below, many elements having useful natural abundance and nuclear spin are naturally present in biomolecules. Still others can be substituted into biological molecules to provide a diverse range of opportunities. For example, fluorine can be substituted for hydrogen in many cases. [Pg.513]

Both the quality of TFP resin and the resulting polymeric-activated resins may be quantitatively determined by 19F NMR spectroscopy.1 This nondestructive technique takes advantage of the high sensitivity, natural abundance (the 1/2 spin nucleus 19F is 100% abundant), and large chemical shift dispersion ( 200 ppm) of the 19F nucleus. The 19F NMR spectrum of TFP resin shows two resonances at 148 and 165 ppm (Fig. 3), each corresponding to 2 equiv. fluorine nuclei. The 19F NMR spectrum of TFP-activated carboxylate and sulfonate resins shows two resonances at ca. [Pg.157]

As Table 3 shows, fluorine-19 has a spin number of 1/2 and a natural abundance of virtually 100% it is thus an ideal nucleus for NMR studies. It has a highmagnetogyric ratio and thus has a similar sensitivity to hydrogen, and so it is not surprising that, since the early days of NMR, fluorine-19 studies of organic, inorganic and organometallic compounds have been widespread. [Pg.270]

All NMR spectra were recorded in SO2CIF solvent at -50 °C except the spectrum, which was recorded at -15 C. The subscripts A and B/X, denote axial and equatorial fluorine atoms, respectively. The 0 NMR parameters for solvent SO2CIF at natural abundance were also determined in the present study doublet at 8( 0), 227.0 ppm V( 0- F), 27.9 Hz. [Pg.399]

PVDF. This polymer can contain head-to-head and tail-to-tail sequences, as illustrated in Figure 7-25. Because the 19F nucleus has a spin number of 1/2 and its natural abundance is 100%. 19F NMR spectroscopy is a powerful tool for studying fluoropolymers like PVDF. The fluorine atoms are the little yellow balls and you ll notice that one of the units in Figure 7-25 has been put in backwards, giving a head-to-head and tail-to-tail sequence. The peaks marked A, B, C and D in the spectrum of PVDF (Figure 7-26) correspond to the fluorine atoms labeled in the same way in the figure. Of course, what you would really like to know is the number fraction of VDF monomers that are incorporated backwards into the chain. This information can be obtained from the relative intensities of the bands, but to extract it we have to revisit probability theory. (Oh no the nightmare continues )... [Pg.184]

Modem mass spectrometers provide a powerful tool for the indentification and study of nonmetal fluorides and their derivatives. Many compounds are sufficiently volatile to make sampling relatively easy. In highly fluorinated compounds, the 100% natural abundance of F simplifies interpretation of many spectra and high-resolution spectra are often not required for unambiguous interpretation of mass spectra. Numerous nomnetal fluorides and derivatives were first identified by mass spectrometry and subsequently obtained in sufficient amounts to characterize by other methods. Modem quadropole mass spectrometers are particularly useful in the analysis of fluorine compounds and their open architecture facilitates the analysis of highly reactive fluorine compounds and compounds of low thermal stability. [Pg.1345]

Although several other important nuclides can be detected by NMR, proton ( H) remains the most widely used because of its high sensitivity, high isotopic natural abundance (99.985%), and ubiquitous presence in organic compounds. Of comparable importance is carbon ( C), 1.108% abundance, which, because of substantial improvements in instrument sensitivity, is now utilized as routinely as proton. Fluorine ( F), 100% abundance, is less used since it is present in only about 10% of pharmaceutical compounds. Another consequence of the intrinsic low sensitivity of NMR is that virtually all samples require signal averaging to reach an acceptable signal-to-noise level. Depend-... [Pg.906]


See other pages where Fluorine natural abundance is mentioned: [Pg.344]    [Pg.63]    [Pg.151]    [Pg.17]    [Pg.151]    [Pg.93]    [Pg.111]    [Pg.434]    [Pg.695]    [Pg.198]    [Pg.256]    [Pg.412]    [Pg.77]    [Pg.327]    [Pg.674]    [Pg.201]    [Pg.244]    [Pg.30]    [Pg.63]    [Pg.434]    [Pg.5]    [Pg.5]    [Pg.20]    [Pg.39]    [Pg.79]    [Pg.627]    [Pg.186]    [Pg.250]    [Pg.326]    [Pg.299]    [Pg.163]    [Pg.151]    [Pg.272]    [Pg.1344]    [Pg.152]    [Pg.63]    [Pg.511]    [Pg.247]    [Pg.299]   
See also in sourсe #XX -- [ Pg.602 ]




SEARCH



Abundance, natural

© 2024 chempedia.info