¹⁸³W NMR spectroscopy of W(VI) imidoaryl and imidoalkyl complexes using inverse detection based on non‐specific long‐range interactions

Abstract

Abstract 183 W NMR spectra for a series of octahedral W(VI) imidophenyl, ‘WNPh’ and W(VI) imidoethyl, ‘WNEt,’ complexes were obtained using inverse detection based on non‐specific long‐range interactions. The metal couples to both the ortho and para protons of the NPh moiety (four and six bonds, respectively). The 183 W shift is shown to be sensitive to the nature of the ligand and the coordination number. The effect of geometric isomerism on δ 183 W is shown to be several hundred ppm. Some δ 14 N and δ 15 N and 1 J ( 183 W, 15 N) data are reported. A number of new geometric isomers, involving the position of the NR ligand with respect to the remaining ligands, have been identified.