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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: J Biomol NMR. 2011 Sep 15;51(3):245–251. doi: 10.1007/s10858-011-9533-1

Fig. 2.

Fig. 2

The four parts of the gsHZQC experiment are depicted as a 2 × 2 grid in which rows denote inversion of the outer multiplet components and columns generate echo/antiecho data. Frequency discrimination is controlled by placing the composite 1H 180° pulse before or after the t1 evolution period, while the phase of the outer multiplet components is controlled by placement of the 13C 180° pulse. Due to variation in the position of the 1H and 13C 180° pulses, the encode gradient must select either zero- or double-quantum coherence (ZQ or DQ), as shown in the coherence level diagrams. For both 1H and 13C, the coherence pathways selected by the encode and decode gradients are shown as solid lines. The relative signs of the encode and decode gradients depict the coherence selection of the pulse sequences in Fig. 1a, c. The dashed boxes are consistent with those of Fig. 1