Slice selective absorption-mode J-resolved NMR spectroscopy.

Limited chemical shift dispersion and broad multiplet patterns limit resolution in H NMR spectra. J-Resolved spectroscopy overcomes this problem to a great extent. However, the phase-twist line shape in J-Resolved spectroscopy allows only the magnitude mode of the experiment to be practical, which degrades resolution. Recently, various pure shift or broadband homonuclear decoupling approaches have been integrated with J-Resolved spectroscopy to eliminate the broad dispersive contribution. In the present work, we demonstrate a broadband H-H J-Resolved spectrum with a greatly reduced dispersive contribution using the concept of slice selection. We show that slice selective excitation, t encoding, storage, and detection of the in-phase absorptive signals can be executed, while a gradient-based suppression of the dispersive antiphase signals can be performed during the storage period. In more than two spin systems, a small part of the doubly antiphase absorptive signal may also contribute to the spectrum in addition to the inphase absorptive signals. The overall effect is a reduced multiplet pattern similar to a regular J-Resolved case as the passive spins remain unflipped due to slice selective pulses. However, the effect is broadband for a fraction of the spins when all slices are considered analogous to Zangger-Sterk (ZS) broadband homo-decoupling. Further, the fresh magnetization from neighboring slices can be accessed in different scans by frequency shifting of the slice selective pulses without a recycle delay-an elegant aspect of the ZS pulse element. This allows faster signal averaging, improving sensitivity which depends on the T relaxation time of the signals. This method displays sensitivity up to 4-20 percent of the regular J-RES H signals.