Details

Autor(en) / Beteiligte

• Elliott, S. J.
• Bengs, C.
• Brown, L. J.
• Hill-Cousins, J. T.
• O’Leary, D. J.
• Pileio, G.
• Levitt, M. H.

Titel

Nuclear singlet relaxation by scalar relaxation of the second kind in the slow-fluctuation regime

Ist Teil von

• The Journal of chemical physics, 2019-02, Vol.150 (6), p.064315-064315

Ort / Verlag

United States: American Institute of Physics

Erscheinungsjahr

2019

Link zum Volltext

Quelle

American Institute of Physics

Beschreibungen/Notizen

• The singlet state of nuclear spin-1/2 pairs is protected against many common relaxation mechanisms. Singlet order, which is defined as the population difference between the nuclear singlet and triplet states, usually decays more slowly than the nuclear magnetization. Nevertheless, some decay mechanisms for nuclear singlet order persist. One such mechanism is called scalar relaxation of the second kind (SR2K) and involves the relaxation of additional nuclei (“third spins”) which have scalar couplings to the spin-1/2 pair. This mechanism requires a difference between the couplings of at least one third spin with the two members of the spin-1/2 pair, and depends on the longitudinal relaxation time of the third spin. The SR2K mechanism of nuclear singlet relaxation has previously been examined in the case where the relaxation rate of the additional spins is on the time scale of the nuclear Larmor frequency. In this paper, we consider a different regime, in which the longitudinal relaxation of the third spins is on a similar time scale to the J-coupling between the members of the spin pair. This regime is often encountered when the spin-1/2 pair has scalar couplings to nearby deuterium nuclei. We show that the SR2K mechanism may be suppressed in this regime by applying a radiofrequency field which is resonant either with the members of the spin pair, or with the third spins. These phenomena are analyzed theoretically and by numerical simulations, and demonstrated experimentally on a diester of [13C2, 2H2]-labeled fumarate in solution.