Low-power broadband homonuclear dipolar recoupling without decoupling: Double-quantum 13C NMR correlations at very fast magic-angle spinning

We report novel symmetry-based radio-frequency (rf) pulse sequences for efficient excitation of double-quantum (2Q) coherences under very fast (>60 kHz) magic-angle spinning (MAS) conditions. The recursively generated pulse-scheme series, R 2 2 p 1 R 2 2 p - 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 14.1 T and 66 kHz MAS, where the pulse schemes with p ⩾ 3 compare favorably to current state-of-the-art recoupling options.