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Fourier transform systems

Although the determination of HA or HB selectivity is relatively straightforward the techniques for isolation of pyridine nucleotides from the reaction mixtures are tedious and time consuming. Two more recent techniques use either proton magnetic resonance or electron impact and field desorption mass spectrometry. The technique of Kaplan and colleagues requires a 220 MHz nuclear magnetic resonance spectrometer interfaced with a Fourier transform system [104], It allows the elimination of extensive purification of the pyridine nucleotide, is able to monitor the precise oxidoreduction site at position 4, can be used with crude extracts, and can be scaled down to /nmole quantities of coenzyme. The method can distinguish between [4-2H]NAD+ (no resonance at 8.95 8) and NAD+ (resonance at 8.95—which is preferred) or between [4A-2H]NADH (resonance at 2.67 8, 75 4B = 3.8 Hz) and [4B-2H]NADH (resonance at 2.77 8, J5 4A = 3.1 Hz). [Pg.86]

Historically, Fourier spectroscopy was developed for use in the far-infrared and mid-infrared spectral regions. Commercially available Fourier transform systems today are operating primarily in these spectral regions. The extension of Fourier transform spectroscopy to shorter wavelengths has been proposed21 22 and demonstrated.23-25 However, rapid commercialization of Fourier transform instrumentation for visible /UV spectroscopy is not occuring. Instead, visible/UV Fourier transform spectroscopy is being done in just a few spectroscopy laboratories with specialized, one-of-a-kind instrumentation. [Pg.422]

Bands of the A - X A system of HO2 and DO2 have also been recorded (13). With oxygen alone, the b Eg - a Ag electric quadrupole transition of O2 (14) has been observed, indicating the sensitivity of the Fourier transform system in the near infrared. [Pg.7]

The frequency of radiation used in NMR depends on the field strength of the magnet used in the instrument. Frequencies range fi om 60 to 600 MHz for commercial instruments. Modem NMR equipment uses RF pulses in Fourier transform systems. There are no safety concerns associated with these frequencies of radiation. [Pg.319]

Durnin [22]. With this condition, the synthesis of diffraction free beams using a Fourier transform system is very simple. [Pg.309]

C-13 NMR spectra of BA, PHBA, and PNP in a series of solvents were recorded at 30°C on a JEOL JNM PS-100 NMR spectrometer equipped with a PFT-100 Fourier transform system at 25.14 MHz. [Pg.567]

Infrared spectra are obtained on a Digilab Model 15 Fourier Transform system at four wavenumber resolution in double beam operation. An adequate signal-to-noise ratio... [Pg.408]

NMR Spectrometer Varian, XLOlOO 15 NMR equipped with Varian FT-100 pulsed NMR Fourier transform system and disc accessory or equivalent. [Pg.409]

In the further manipulations the site representation will be used for convenience. The Fourier transform with respect to time of a single-exciton retarded Green s function (t) of a system under the Hamiltonian in the site representation for exciton coordinates and Fock s representation for phonon coordinates is written as... [Pg.446]

Woodruff and co-workers introduced the expert system PAIRS [67], a program that is able to analyze IR spectra in the same manner as a spectroscopist would. Chalmers and co-workers [68] used an approach for automated interpretation of Fourier Transform Raman spectra of complex polymers. Andreev and Argirov developed the expert system EXPIRS [69] for the interpretation of IR spectra. EXPIRS provides a hierarchical organization of the characteristic groups that are recognized by peak detection in discrete ames. Penchev et al. [70] recently introduced a computer system that performs searches in spectral libraries and systematic analysis of mixture spectra. It is able to classify IR spectra with the aid of linear discriminant analysis, artificial neural networks, and the method of fe-nearest neighbors. [Pg.530]

As mentioned, we also carried out IR studies (a fast vibrational spectroscopy) early in our work on carbocations. In our studies of the norbornyl cation we obtained Raman spectra as well, although at the time it was not possible to theoretically calculate the spectra. Comparison with model compounds (the 2-norbornyl system and nortri-cyclane, respectively) indicated the symmetrical, bridged nature of the ion. In recent years, Sunko and Schleyer were able, using the since-developed Fourier transform-infrared (FT-IR) method, to obtain the spectrum of the norbornyl cation and to compare it with the theoretically calculated one. Again, it was rewarding that their data were in excellent accord with our earlier work. [Pg.143]

It is interesting to note that a similar specttum of the 0-0 band of the a-X system, leading to the same value of the absorption intensity, has been obtained using a Fourier transform spectrometer (see Section 3.3.3.2) but with an absorption path, using a multiple reflection cell, of 129 m and half the pressure of gas. [Pg.385]

Fig. 3. A block diagram schematic representation of a Fourier transform nmr spectrometer, ie, a superconducting magnetic resonance system. Fig. 3. A block diagram schematic representation of a Fourier transform nmr spectrometer, ie, a superconducting magnetic resonance system.
Infrared (in) spectrometers are gaining popularity as detectors for gas chromatographic systems, particularly because the Fourier transform iafrared (ftir) spectrometer allows spectra of the eluting stream to be gathered quickly. Gc/k data are valuable alone and as an adjunct to gc/ms experiments. Gc/k is a definitive tool for identification of isomers (see Infrared and raman spectroscopy). [Pg.108]

The (5-part in (2.50) is responsible for elastic scattering, while the second term, proportional to the Fourier transform of C(t), leads to the gain and loss spectral lines. When the system exercises undamped oscillations with frequency Aq, this leads to two delta peaks in the structure factor. [Pg.24]


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