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Jeener-Broekaert dipolar order relaxation

C. Jeener-Broekaert dipolar order relaxation sequence 464... [Pg.405]

C. Jeener-Broekaert Dipolar Order Relaxation Sequence... [Pg.464]

The classical Jeener Broekaert sequence (133) is used to determine the dipolar-order relaxation time (in systems of spin 1/2 nuclides) and the Tiq relaxation time (in systems with spin 1 nuclides) of spin 1 nuclides with quadrupolar contributions to 7. Its FFC version is similar to the Inversion Recovery, except that the first 180° pulse is replaced by the sequence 90, — 5 — 45, the detection pulse becomes 45 and a special phase cycle is required. We shall not dwell on the details and purpose of the sequence since they go beyond the scope of this chapter. We wish to underline, however, the fact that sequences of this type require a close coordination of the preparatory sub-sequence with the signal-detection sub-sequence in order to isolate not just a particular magnetization component but a particular relaxation pathway. [Pg.464]

Jeener and Broekaert introduced, in 1%7, a three-pulse B,(r) sequence to measure the relaxation time Tm of the dipolar order of / = 1 spin systems in the presence of a conventional high Zeeman field, Bq, which is based on the decay time of the so-called Jeener echo . It was later extended by Spiess and Kemp-Harper and Wimperis to study in a similar way the quadrupolar order in / a 1 systems. The appearance of a Jeener echo depends upon the existence of interactions that are not averaged out by molecular motions on the considered time scale. The method has become of great importance in recent relaxation studies, in particular of liquid crystals because, in standard spin relaxation theories, it provides a power l means to separate and analyse the spectral densities / v) and /2) j. i4,is,2025 ggg... [Pg.23]


See other pages where Jeener-Broekaert dipolar order relaxation is mentioned: [Pg.79]    [Pg.88]    [Pg.290]    [Pg.593]   


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