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

✍ Scribed by Alceo Macchioni; Paul S. Pregosin; Heinz Rüegger; Gerard van Koten; Paul A. van der Schaaf; Rob A. T. M. Abbenhuis


Book ID
102951543
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
524 KB
Volume
32
Category
Article
ISSN
0749-1581

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✦ Synopsis


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.