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1 We report the formation of a stable neutral diboron diradical simply by coordination of an aromatic dinitrogen compound to an ortho-phenyldiborane.
2 Oxygen is a diradical and because of its unique electronic configuration, it has the potential to form strong oxidants (e.g.
3 All mechanistic results are in agreement with a triplet reaction pathway and with the intermediacy of a 1 , 4 - diradical .
4 Examples are provided of its application to imaging of nitroxide radicals, diradicals , and spin-trapped radicals at a Larmor frequency of ca.
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Diradical through the time