[en] Boron difluoride (BF${}_2$) formazanate dyes are contenders for molecular species that exhibit a large Stokes shift and bright red emission. Excitation of 3-cyanoformazanate complexes with 10 μs wide pulses of specific wavelengths resulted in strong luminescence at 663 nm at both room temperature in solution and at 77 K in a frozen solution. Analysis of the short-lived excitation spectrum from this luminescence shows that it arises from a vibronic manifold of a higher-lying excited state. This dark state relaxes to the emitting state over 10 μs. TD-DFT calculations of the two lowest-energy excited states show that the relaxed geometries are planar for S${}_1$ but highly distorted in S${}_2$. The specific time- and wavelength-dependence of the excitation profile provides a unique optical encryption capability through the comparison of emission intensities between adjacent vibronic bands only accessible in the 0-12 μs time domain. (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)