Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 157, Issue 13, Pages -Publisher
AIP Publishing
DOI: 10.1063/5.0103122
Keywords
-
Funding
- European Research Council [786707-FunMagResBeacons]
- EPSRC-UK [EP/P009980/1, EP/P030491/1, EP/V055593/1]
Ask authors/readers for more resources
Coupled pairs of spin-1/2 nuclei can form one singlet state and three triplet states. The nuclear singlet order, which is the difference between the singlet population and the mean of the triplet populations, is a long-lived state in solution. The PulsePol pulse sequence, based on the theory of symmetry-based recoupling sequences, is an efficient technique for generating long-lived singlet order from magnetization in nuclear magnetic resonance (NMR). This study introduces new pulse sequences for singlet-triplet excitation and conversion in solution NMR and demonstrates schemes to enhance their robustness.
Coupled pairs of spin-1/2 nuclei support one singlet state and three triplet states. In many circumstances, the nuclear singlet order, defined as the difference between the singlet population and the mean of the triplet populations, is a long-lived state that persists for a relatively long time in solution. Various methods have been proposed for generating singlet order, starting from nuclear magnetization. This requires the stimulation of singlet-to-triplet transitions by modulated radiofrequency fields. We show that a recently described pulse sequence, known as PulsePol [Schwartz et al., Sci. Adv., 4, eaat8978 (2018)], is an efficient technique for converting magnetization into long-lived singlet order. We show that the operation of this pulse sequence may be understood by adapting the theory of symmetry-based recoupling sequences in magic-angle-spinning solid-state nuclear magnetic resonance (NMR). The concept of riffling allows PulsePol to be interpreted by using the theory of symmetry-based pulse sequences and explains its robustness. This theory is used to derive a range of new pulse sequences for performing singlet-triplet excitation and conversion in solution NMR. Schemes for further enhancing the robustness of the transformations are demonstrated. (C) 2022 Author(s).All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY)license (http://creativecommons.org/licenses/by/4.0/).
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available