Abstract
A new application of the stimulated echo pulse sequence is presented that permits the elucidation of molecular order and dynamics in a time scale between about 100 μs and the spin-lattice relaxation time. The technique exploits the influence of dipolar coupling on the quotient of the amplitudes of the stimulated and primary echoes produced by the standard three 90°-pulse sequence. Results obtained for a nematic liquid crystal in bulk and confined in porous glass (mean pore diameter 4 nm) are compared. In both cases the echo amplitude quotient oscillates as a function of the pulse spacing. In a bulk nematic crystal these oscillations originate from strong unaveraged dipolar interactions and directly reflect the molecular order in the material. In porous glass a real nematic order is absent. In this case, the oscillations can be attributed to spin exchange between inequivalent protons. Exchange rates are estimated.
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 callDisclaimer: 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.
