Book by Timothy Claridge "High-Resolution NMR Techniques in Organic Chemistry" recommends calibrating homonuclear decoupling pulse power using Bloch-Siegert shift. It's somewhere in the "calibrations" section of the book.
Is there a particular reason that it would be inaccurate to set decoupler directly on resonance and calibrate width of 90 degree pulse by finding 360 pulse zero crossing?
Thanks.