Heteronuclear Polarization Transfers Between Spin-locked and Anti-Longitudinal Spin States in the NMR of Liquids and Spinning Solids
Sundaresan Jayanthi, Adonis Lupulescu, Julia Grinshtein, Lucio Frydman

TL;DR
This paper extends a novel polarization transfer scheme to powder NMR under MAS and solution conditions, deriving the average Hamiltonian and demonstrating maximum polarization enhancement through second-order interactions.
Contribution
It develops a theoretical framework for heteronuclear polarization transfer in liquids and solids, validated by experiments and simulations, with potential for enhanced NMR sensitivity.
Findings
Maximum polarization enhancement equals the ratio of gyromagnetic ratios.
Transfer occurs without pulsing on the abundant spins.
The process is oscillatory and involves second-order average Hamiltonians.
Abstract
Recently, Pang et al reported a novel polarization transfer scheme applicable to three-spin systems, whereby a rotating-frame NMR analogue of the cross effect could transfer polarization between; e.g., two 13Cs and an 15N in a single crystal. The present work furthers this scheme to the case of powder NMR under magic angle spinning (MAS) conditions, as well as to solution NMR. It is found that in all such cases a second-order average Hamiltonian can transfer polarization between non-equivalent, coupled abundant spins (e.g., two 1Hs) prepared in anti-longitudinal magnetization states, and the spin-locked magnetization of a rare spins (e.g., one 13C). The average Hamiltonian for such three-spin (S1-S2) to I transfer was derived for both liquids and solids, and found in good quantitative agreement with numerical simulations and experiments. At an optimal transfer condition whereby an…
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