Characterization of a Triplet Vinylidene

Singlet vinylidenes (R2C=C:) are proposed as intermediates in a series of organic reactions, and very few have been studied by matrix isolation or gas-phase spectroscopy. Triplet vinylidenes, however, featuring two unpaired electrons at a monosubstituted carbon atom are thus far only predicted as electronically excited-state species and represent an unexplored class of carbon-centered diradicals. We report the photochemical generation and low-temperature EPR/ENDOR characterization of the first ground-state high-spin (triplet) vinylidene. The zero-field splitting parameters (D = 0.377 cm(-1) and vertical bar E vertical bar/D = 0.028) were determined, and the C-13 hyperfine coupling tensor was obtained by C-13-ENDOR measurements. Most strikingly, the isotropic C-13 hyperfine coupling constant (50 MHz) is far smaller than the characteristic values of triplet carbenes, demonstrating a unique electronic structure which is supported by quantum chemical calculations.