Abstract
We report novel symmetry-based radio-frequency (rf) pulse sequences for efficient excitation of double-quantum (2Q) coherences under very fast (>60kHz) magic-angle spinning (MAS) conditions. The recursively generated pulse-scheme series, R22p1R22p-1(p=1,2,3,…), offers broadband 13C–13C recoupling in organic solids at a very low rf power. No proton decoupling is required. A high-order average Hamiltonian theory analysis reveals a progressively enhanced resonance-offset compensation for increasing p, as verified both by numerical simulations and 2Q filtration NMR experiments on 13C2-glycine, [2,3-13C2]alanine, and [U–13C]tyrosine at 14.1T and 66kHz MAS, where the pulse schemes with p⩾3 compare favorably to current state-of-the-art recoupling options.
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