Despite the existence of the
closed-shell Kekulé structure, O=C=C=O, the lowest bound state of ethyledione is a
triplet. It would then be a
diradical, with an
electronic structure motif similar to the
oxygen molecule. However, when the molecule is distorted away from its equilibrium geometry, the potential surfaces of the triplet and
singlet states intersect, allowing for
intersystem crossing to the singlet state, which is unbound and dissociates to two ground-state CO molecules. The timescale of the intersystem crossing was predicted to be 0.5
ns, making triplet ethylenedione a transient, yet spectroscopically long-lived molecule. On the other hand, the mono
anion of ethylenedione, OCCO−, as well as the dianion , called
acetylenediolate, are both stable. Recent theoretical computations suggest that the
in situ preparation and characterization of ethylenedione may be possible through low-energy free-electron induced single-molecule engineering. ==Koch's glyoxylide==