The cryogenic, matrix-isolated ESR and electronic spectroscopy of a set of
quarter state organic phenylnitreno-radicals are described, using nitronyln
itroxide, benzo-nitronylnitroxide, and verdazyl radical spin sites, and bot
h meta and para a connectivities. Delocalization of the nitrene unit in the
para-linked series is not extensive, judging by the computational results.
The ESR spectral results show that zero-field splitting is affected much m
ore by the connectivity in the systems (para versus meta) than by structura
l variations within the nitreno-radical theme. (C) 2001 Elsevier Science Lt
d. All rights reserved.