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Stimulated-echo pulse sequences

The DDIF experiment consists of a stimulated echo pulse sequence [50] and a reference scan to measure and separate the effect of spin-lattice relaxation. The pulse diagrams for these two are shown in Figure 3.7.2. Details of the experiments have been discussed in Ref. [51] and a brief description will be presented here. [Pg.345]

Fig. 10. The stimulated-echo pulse sequence used in this work for projection imaging of the z component of the velocity over the whole sample. Fig. 10. The stimulated-echo pulse sequence used in this work for projection imaging of the z component of the velocity over the whole sample.
Figure 9 (a) Stimulated echo pulse sequence with length of gradient pulse S and diffusion time A longimdinal and transverse relaxation takes place within the time intervals as indicated, (b) Stimulated echo sequence with longimdinal prerelaxation. [Pg.289]

Figurel. Bipolar stimulated echo pulse sequence (BPPSTE). The gradient time <5 T, t1 and x2 delays were set to 2 ms, 20 ms, 68ps and 78ps, respectively. (Reproduced with permission from Polym. Prepr. 2001,42.1, 23-24. Figurel. Bipolar stimulated echo pulse sequence (BPPSTE). The gradient time <5 T, t1 and x2 delays were set to 2 ms, 20 ms, 68ps and 78ps, respectively. (Reproduced with permission from Polym. Prepr. 2001,42.1, 23-24.
Pulsed field gradient spin echo NMR is generally the method of choice for diffusion measurements on liquid samples (see Section 5.1 in this chapter). With modem high field instruments, however, severe problems can arise when it is applied to samples with very high proton concentrations because of the presence of radiation damping. Connel et al reduced the problems by a suitable choice of experimental parameters, in particular the use of modified stimulated echo pulse sequences with a reduced flip angle for the first pulse. [Pg.234]

The stated aim of this review is to demonstrate that elassical analyses of physieal organie ehemistry are feasible with respect to complex systems such as supported metal catalysts through the application of advanced EMR spectroscopic techniques and determining the relevant spin Hamiltonian parameters via the Zeeman-dependent hyperfine spectrum. The principles of analysis were outlined in the preceding section and entail replicate collection of ESEEM or ENDOR spectra by incremental steps and mapping the trajectory of peak positions. Deconvolution of peaks may be made either by traditional tau-suppression in the stimulated echo pulse sequence or via advanced pulse sequences such as HYSCORE (2-D ESEEM, Hofer, 1994). Mapping of spectral peak position as it varies depending on the Zeeman field is very important to the accurate determination of hyperfine terms. [Pg.130]

Diffusion-relaxation correlation has been utilized to study biological tissues, e.g., compartmentalization in tissues [32-35]. In many reports, a sequence that combines a stimulated echo-type sequence with a pulsed field gradient and a CPMG as a detection has been described [35]. Other pulses sequences have also been used to study the diffusion-relaxation correlation, e.g., Ref. [36]. [Pg.166]

Left two-pulse [(a) primary ESEEM] and three-pulse [(b) stimulated echo ESEEM] sequences t is the (fixed) delay time between pulses one and two and T is a variable delay time. Right frequency domain and time domain (inset) of the two-pulse EESEM spectrum of VO - vanabin, recorded at the m = — 1 /2 line, at 77 K and a pulse width of 20 ns.P l The superhyperfine coupling constant = 4.5 MHz (obtained from the N double-quantum lines at 3.9 and 7.1 MHz) is in accord with amine nitrogen provided by lysines of the vanadium-binding protein. The spin echo due to proton coupling, at 13.7 MHz, was also observed. Reproduced from K. Eukui et al., J. Am. Chem. Soc. 125, 6352-6353. Copyright (2003), with permission from the American Chemical Society. [Pg.76]

Fig. 9. Modifications to the basic PFG spin-echo pulse sequence (a) stimulated echo (b) addition of alternating pulse gradients (c) addition of longitudinal eddy-current delay period. Fig. 9. Modifications to the basic PFG spin-echo pulse sequence (a) stimulated echo (b) addition of alternating pulse gradients (c) addition of longitudinal eddy-current delay period.
Fig. 4. iR spectra of EMIm measured with (a) single pulse, (b) Hahn (PGSE) and (c) stimulated echo (STE) sequences. The STE echo signals were measured with small and short PFGs. [Pg.215]

Figure Bl.15.11. Fomiation of electron spin echoes. (A) Magnetization of spin packets i,j, /rand / during a two-pulse experiment (rotating frame representation). (B) The pulse sequence used to produce a stimulated echo. In addition to this echo, which appears at r after the third pulse, all possible pairs of the tluee pulses produce primary echoes. These occur at times 2x, 2(x+T) and (x+2T). Figure Bl.15.11. Fomiation of electron spin echoes. (A) Magnetization of spin packets i,j, /rand / during a two-pulse experiment (rotating frame representation). (B) The pulse sequence used to produce a stimulated echo. In addition to this echo, which appears at r after the third pulse, all possible pairs of the tluee pulses produce primary echoes. These occur at times 2x, 2(x+T) and (x+2T).
Muns ENDOR mvolves observation of the stimulated echo intensity as a fimction of the frequency of an RE Ti-pulse applied between tlie second and third MW pulse. In contrast to the Davies ENDOR experiment, the Mims-ENDOR sequence does not require selective MW pulses. For a detailed description of the polarization transfer in a Mims-type experiment the reader is referred to the literature [43]. Just as with three-pulse ESEEM, blind spots can occur in ENDOR spectra measured using Muns method. To avoid the possibility of missing lines it is therefore essential to repeat the experiment with different values of the pulse spacing Detection of the echo intensity as a fimction of the RE frequency and x yields a real two-dimensional experiment. An FT of the x-domain will yield cross-peaks in the 2D-FT-ENDOR spectrum which correlate different ENDOR transitions belonging to the same nucleus. One advantage of Mims ENDOR over Davies ENDOR is its larger echo intensity because more spins due to the nonselective excitation are involved in the fomiation of the echo. [Pg.1581]

Figure B2.1.10 Stimulated photon-echo peak-shift (3PEPS) signals. Top pulse sequence and iuterpulse delays t and T. Bottom echo signals scaimed as a fiinction of delay t at tluee different population periods T, obtained with samples of a tetrapyrrole-containing light-harvesting protein subunit, the a subunit of C-phycocyanin. Figure B2.1.10 Stimulated photon-echo peak-shift (3PEPS) signals. Top pulse sequence and iuterpulse delays t and T. Bottom echo signals scaimed as a fiinction of delay t at tluee different population periods T, obtained with samples of a tetrapyrrole-containing light-harvesting protein subunit, the a subunit of C-phycocyanin.
Another approach to obtain spatially selective chemical shift information is, instead of obtaining the entire image, to select only the voxel of interest of the sample and record a spectrum. This method called Volume Selective spectroscopY (VOSY) is a ID NMR method and is accordingly fast compared with a 3D sequence such as the CSI method displayed in Figure 1.25(a). In Figure 1.25(b), a VOSY sequence based on a stimulated echo sequence is displayed, where three slice selective pulses excite coherences only inside the voxel of interest. The offset frequency of the slice selective pulse defines the location of the voxel. Along the receiver axis (rx) all echoes created by a stimulated echo sequence are displayed. The echoes V2, VI, L2 and L3 can be utilized, where such multiple echoes can be employed for signal accumulation. [Pg.44]

Fig. 2.7.2 Diffusion-relaxation correlation se- The detection (2nd) segment for both is a quences using pulsed field gradients, (a) The CPMG pulse train that is similar to that in first segment is a spin-echo with the echo Figure 2.7.1. The amplitude or the duration of appearing at a time 2tcpi after the first pulse, the gradient pairs in both sequences is (b) The first segment is a stimulated echo incremented to vary the diffusion effects, appearing at a time tcpi after the third pulse. Fig. 2.7.2 Diffusion-relaxation correlation se- The detection (2nd) segment for both is a quences using pulsed field gradients, (a) The CPMG pulse train that is similar to that in first segment is a spin-echo with the echo Figure 2.7.1. The amplitude or the duration of appearing at a time 2tcpi after the first pulse, the gradient pairs in both sequences is (b) The first segment is a stimulated echo incremented to vary the diffusion effects, appearing at a time tcpi after the third pulse.
The reference scan is to measure the decay due to spin-lattice relaxation. Compared with the corresponding stimulated echo sequence, the reference scan includes a jt pulse between the first two jt/2 pulses to refocus the dephasing due to the internal field and the second jt/2 pulse stores the magnetization at the point of echo formation. Following the diffusion period tD, the signal is read out with a final detection pulse. The phase cycling table for this sequence, including 2-step variation for the first three pulses, is shown in Table 3.7.2. The output from this pair of experiments are two sets of transients. A peak amplitude is extracted from each, and these two sets of amplitudes are analyzed as described below. [Pg.345]

Fig. 4.5.5 Pulsed field gradient sequences to obtain velocity and diffusion data (a) spin-echo (PGSE) and (b) stimulated-echo (PGSTE). The application of imaging gradients C Gy and Gz allows the measurement of velcocity maps and spatially-resolved diffusion coefficients and size distribution in emulsions. Fig. 4.5.5 Pulsed field gradient sequences to obtain velocity and diffusion data (a) spin-echo (PGSE) and (b) stimulated-echo (PGSTE). The application of imaging gradients C Gy and Gz allows the measurement of velcocity maps and spatially-resolved diffusion coefficients and size distribution in emulsions.
Fig. 5.3.4 (A) Stimulated echo dynamic NMR microscopy pulse sequence. The first field gradient pulse (g,) of duration 8 serves to encode spatial positions of spins and the second field gradient pulse has a refocusing effect. Fig. 5.3.4 (A) Stimulated echo dynamic NMR microscopy pulse sequence. The first field gradient pulse (g,) of duration 8 serves to encode spatial positions of spins and the second field gradient pulse has a refocusing effect.

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See also in sourсe #XX -- [ Pg.133 , Pg.134 ]




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Echo pulse sequence

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Pulse double stimulated echo sequence

Pulse echo

Pulse sequenc

Pulse sequence

Pulse stimulated echo diffusion sequenc

Pulse-field gradient-stimulated echo sequence

Stimulated-echo sequence

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