Abstract
A phase-modulation technique for coherent Raman spectroscopy is used to measure both the real and imaginary parts of the third-order nonlinear susceptibility of gases. The Raman Q-branch resonance of D2 is calibrated by comparison to the Q-branch resonance of N2. By using D2 as an internal standard, the nonresonant electronic susceptibility of Ar and the sum of the electronic and molecular reorientation contributions to the nonresonant susceptibility of N2 are determined. The results of these measurements are compared to published data on the Q-branch Raman cross section of H2, to predictions from the theory of the optical (ac) Kerr effect, and to measurements of electronic hyperpolarizabilities. For the last-mentioned quantity, measurements from three-wave mixing, from field-induced second-harmonic generation, from third-harmonic generation, and from the electro-optic (dc) Kerr effect are intercompared and agreement at the 10% level is established. Formulas interrelating a number of different definitions of third-order susceptibilities found in the literature are presented.

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