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Pulse interferogram

Figure 1.7. Pulse interferogram and FT NMR spectrum of glycerol, DOCH2)2CHOD, [020, 25 °C, 100 MHz]... Figure 1.7. Pulse interferogram and FT NMR spectrum of glycerol, DOCH2)2CHOD, [020, 25 °C, 100 MHz]...
If NMR spectra are computed by Fourier transformation of pulse interferograms (Chapter 2), complex quantities are used during computation. Real and imaginary components v (o>) and i u(io) of the NMR spectrum are obtained as a result. Magnitude or power spectra P io) can be computed from the real and imaginary parts as follows ... [Pg.14]

In most pulsed NMR experiments, the rf field is applied off-resonance. Modulated pulse interferograms (Fig. 2.4(e), 2.5(a), 2.6(a), and 2.7(a)) arise because the vectors of transverse magnetization do not precess with a constant phase shift of itj2 relative to the vector Bj. This is demonstrated in Fig. 2.8. The transverse magnetization is then a resultant of two components, t>(f) with a phase shift of n/2 relative to B, and u(r) in phase with Bt ... [Pg.28]

When several pulse interferograms must be accumulated in order to improve the signal noise ratio, x is the minimum repetition time between two pulses or the minimum pulse interval. [Pg.30]

Fig. 2.14. 22.63 MHz PFT 13C NMR spectra of 3-methyl-5,6,7,8-tetrahydroquinoline 200 mg/mL deuteriochloroform proton decoupled 512 accumulated pulse interferograms pulse width 10 ps pulse interval 0,4 s ... Fig. 2.14. 22.63 MHz PFT 13C NMR spectra of 3-methyl-5,6,7,8-tetrahydroquinoline 200 mg/mL deuteriochloroform proton decoupled 512 accumulated pulse interferograms pulse width 10 ps pulse interval 0,4 s ...
Fig. 2.16. Phase corrected 22.63 MHz PFT 1 C NMR spectrum of mutarotated D-galactose 100 mg/mL deuterium oxide 30 C proton decoupled 512 accumulated pulse interferograms ... Fig. 2.16. Phase corrected 22.63 MHz PFT 1 C NMR spectrum of mutarotated D-galactose 100 mg/mL deuterium oxide 30 C proton decoupled 512 accumulated pulse interferograms ...
An obvious way to avoid signal noise attenuation for slowly relaxing carbons is to add a delay time to the pulse interval. This relaxation delay should be at least in the order of 3 7]. However, accumulation of pulse interferograms becomes time consuming by this method. [Pg.39]

Fig. 3.8. 22.63 MHz PFT t3C lH NMR spectrum of glycylalaninc 0.3 mol/L in deuterium oxide pll = 3.4 25 C 2048 accumulated pulse interferograms pulse width 5 ps pulse interval 0,4 s magnitude internal reference D = 1,4-dioxane ... Fig. 3.8. 22.63 MHz PFT t3C lH NMR spectrum of glycylalaninc 0.3 mol/L in deuterium oxide pll = 3.4 25 C 2048 accumulated pulse interferograms pulse width 5 ps pulse interval 0,4 s magnitude internal reference D = 1,4-dioxane ...
Fig. 5.5. PFT 13C f1 - NMR spectrum of D-glucose, 20 MHz, 1 mol/L in D20, temperature 30 °C, 90 °C pulses accumulation of 200 pulse interferograms (a) series of spectra recorded 15, 30, 45, 60, 75 and 90 min. after sample preparation (b) spectrum of the same sample, recorded 12hrs. after sample preparation. Fig. 5.5. PFT 13C f1 - NMR spectrum of D-glucose, 20 MHz, 1 mol/L in D20, temperature 30 °C, 90 °C pulses accumulation of 200 pulse interferograms (a) series of spectra recorded 15, 30, 45, 60, 75 and 90 min. after sample preparation (b) spectrum of the same sample, recorded 12hrs. after sample preparation.
Fig. 5.6. PFT 1 1H NMR spectra of D-ribose, 22.63 MHz. 1 g/2 mL D20, temperature 30 C, accumulation of 2000 pulse interferograms (6 K data points), 90 pulses, pulse interval 6 s, 2500 Hz, the numbers of the signals refer to the numbering of the C atoms. A quantitative evaluation of the spectrum gave 62% of /j-ribopyranosc (P (i), 20.3% of a-ribopyranose (Pa). 11.6% of /1-ribo-furanose (Ffi) and 6.1 % of a-ribofuranose (Fa) [132b],... Fig. 5.6. PFT 1 1H NMR spectra of D-ribose, 22.63 MHz. 1 g/2 mL D20, temperature 30 C, accumulation of 2000 pulse interferograms (6 K data points), 90 pulses, pulse interval 6 s, 2500 Hz, the numbers of the signals refer to the numbering of the C atoms. A quantitative evaluation of the spectrum gave 62% of /j-ribopyranosc (P (i), 20.3% of a-ribopyranose (Pa). 11.6% of /1-ribo-furanose (Ffi) and 6.1 % of a-ribofuranose (Fa) [132b],...

See other pages where Pulse interferogram is mentioned: [Pg.5]    [Pg.32]    [Pg.25]    [Pg.26]    [Pg.28]    [Pg.30]    [Pg.30]    [Pg.31]    [Pg.33]    [Pg.34]    [Pg.39]    [Pg.42]    [Pg.5]    [Pg.5]    [Pg.5]    [Pg.9]    [Pg.9]    [Pg.138]    [Pg.32]    [Pg.5]    [Pg.203]   
See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.5 ]




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Pulse interferograms

Pulse interferograms

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