The dynamics of four 1-alkyl-3-methylimidazolium bis-(trifluoromethylsulfonyl)imide room-temperature ionic liquids (RTILs) with carbon chain lengths of 2, 4, 6, and 10 were studied by measuring the orientational and spectral diffusion dynamics of the vibrational probe SeCN-. Vibrational absorption spectra, two-dimensional infrared (2D IR), and polarization-selective pump probe (PSPP) experiments were performed on the CN stretch. In addition, optical heterodyne-detected optical Kerr effect (OHD-OKE) experiments were performed on the bulk liquids. The PSPP experiments yielded triexponential anisotropy decays, which were analyzed with the wobbling-in-a-cone model. The slowest decay, the complete orientational randomization, slows with increasing chain length in a hydrodynamic trend consistent with the increasing viscosity. The shortest time scale wobbling motions are insensitive to chain length, while the intermediate time scale wobbling slows mildly as the chain length increases. The 2D IR spectra measured in parallel (< XXXX >) and perpendicular (< XXYY >) polarization configurations gave different decays, showing that reorientation-induced spectral diffusion (RISD) contributes to the dynamics. The spectral diffusion caused by the RTLL structural fluctuations was obtained by removing the RISD contributions. The faster structural fluctuations are relatively insensitive to chain length. The slowest structural fluctuations slow substantially when going from Emim (2 carbon chain) to Bmim (4 carbon chain) and slow further, but more gradually, as the chain length is increased. It was shown previously that K+ causes local ion clustering in the Emim RTIL. The K+ effect increases with increasing chain length. The OHD-OKE measured complete structural randomization times slow substantially with increasing chain length and are much slower than the dynamics experienced by the SeCN- located in the ionic regions of the RTILs.