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Isomeric p- and m-disilaquinodimethanes 2 and 4 were synthesized by the reductive dehalogenation of the corresponding p- and m-bis(halosilyl)benzenes 1 and 3, respectively, and were isolated and structurally characterized. The X-ray diffraction and solid-state NMR studies of 2 revealed its singlet quinodimethane structure featuring two exocyclic Si═C double bonds with some singlet biradical contribution. In contrast, the X-ray crystallography and EPR measurements of 4 disclosed its biradical nature, described as a triplet ground state bis(silyl radical).
Nozawa et al. (Mon,) studied this question.
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