Abstract

A method for measuring nuclear magnetic spin-lattice relaxation in solids in the effective field He3 acting in the triply rotating frame (TRF) is described. The method advances the previously described techniques whereby nuclear magnetic resonance and relaxation in the rotating (RF) and doubly rotating frames (DRF) are measured directly. In the present work, the RF and DRF are employed for suppressing the secular part of nuclear dipole-dipole (DD) interactions in the first two orders. As a result, the higher-order DD interactions (four- and five-particle ones) were separated, and their contribution to the nuclear spin-lattice relaxation in the TRF was studied experimentally. The experiments were carried out on protons in polycrystalline benzene. With the introduced technique, an overall spin-lattice relaxation decay in the TRF was recorded continuously during a single radio-frequency pulse with a length not exceeding 1 s. The contribution of multiproton nonsecular DD interactions to the proton spin-lattice relaxation in the TRF was observed selectively as a pronounced local minimum in the temperature dependence of the relaxation timeT 1ϱϱϱ. This contribution corresponds to ultraslow motion of benzene molecules with a rate about γHe3 ≈ 2π · (101-103) s-1 and is determined quantitatively by specific correlation functions corresponding to the multiparticle nonsecular DD interactions of protons. The prospects of using this method for studying ultraslow atomic and molecular dynamics in solids are discussed.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.