The unprecedented, fully deprotonated form of acetonitrile, the acetonitriletriide anion CCN , is experimentally realized for the first time in the stabilizing bulk host framework of the Ba [TaN ][C N] nitridometalate via a one-pot synthesis from the elements under moderate conditions (920 K). The molecular structure of this long-sought acetonitrile derivative is confirmed by X-ray diffraction, as well as NMR, IR, and Raman spectroscopy. The anion is isoelectronic to the CO molecule, and, in contrast to acetonitrile (H C-C≡N), the electron pairs are shifted towards two double bonds, that is, [C=C=N] .
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