“…5(a)) and full revival of N 2 with three quarter revival of O 2 ( Fig. 5(b)) given by the expression of R(t) = n 2,rot ∞ J=0 F J sin(−ω J t), where n 2,rot = 32β 2 (ω)π 2 N/hcn 0 is the overall magnitude of the rotational Raman effect, ω J = 4πBc(2J + 3) is the angular frequency difference between the coupled rotational levels, B, N, h, c, n 0 , and β(ω) are the rotational constant of the molecule, the density of the considered gas, Planck's constant, the speed of light, linear refractive index at the laser wavelength, and the anisotropy of the molecular polarizability, respectively [44] . F J = (ρ J+2 − ρ J )Z J (J + 2)(J + 1)/(2J + 3) is a function of the transition moment between two coupled rotational levels (J+2 and J), of the population difference (ρ J+2 −ρ J ) between these levels and of a weighting factor Z J describing the multiplicity of each level.…”