Solid‐state heteronuclear multiple‐quantum spectroscopy under a magic‐angle spinning frequency of 150kHz

Abstract

AbstractWe hereby demonstrate that1H detected15N‐1H heteronuclear multiple‐quantum spectroscopy can be carried out at a magic angle spinning frequency of 150 kHz. While the15N‐1H multiple‐quantum coherences can be directly excited from the dipolar order created by the method of adiabatic demagnetization in the rotating frame, it is technically more advantageous to acquire the chemical shift evolution of the heteronuclear multiple‐quantum coherence by two separate chemical shift evolution periods for1H and15N. We also show that the heteronuclear multiple‐quantum correlation spectrum can be obtained by shearing the corresponding heteronuclear single‐quantum correlation spectrum.