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Updated: Aug 3, 2026

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR
Published on: February 23, 2016
Multinuclear PGSE diffusion and overhauser NMR studies on a variety of salts in THF solution
Ignacio Fernández1, Eloísa Martínez-Viviente, Paul S Pregosin
1Laboratory of Inorganic Chemistry, ETHZ HCI Hönggerberg CH-8093 Zurich, Switzerland.
Abstract:
(1)H, (19)F, and (7)Li pulsed gradient spin-echo (PGSE) NMR measurements for a series of salts are reported. The (7)Li is shown to complement the (1)H and (19)F measurements; however, the use of higher concentrations (for the less-sensitive (7)Li) can lead to aggregation. For all of the salts discussed {Li(BF(4)); (n-Bu(4)N)(BF(4)), a trinuclear Ru cluster; [Ir(1,5-COD)(4)](BF(4)), where 4 is a chiral P,N ligand; and the crown ether stabilized potassium salt, [K(18-crown-6)(NPh(2))], 6}, the use of THF seems to promote strong ion pairing. In several cases, the degree of ion pairing approaches 100%. In THF solution, the potassium salt, 6, prefers to exist as a more classical ion pair rather than as the pi complex found in the solid state. In some cases, (1)H, (1)H NOESY and (1)H, (19)F HOESY spectra help to pinpoint the cation/anion spatial relationship.
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