Contribution of the asymmetric stretch, nu3B1, to the fundamental Raman spectrum of water.

The OD-stretching overtone from liquid D2O, 2nu, and the fundamental OD stretch from dilute HDO, both display high-frequency depolarization ratio minima, but the fundamental OD stretch from neat D2O displays a maximum, at the equivalent position. The rhoL minima arises from the decreased depolarization ratio produced by the absence of B1 modes. The fundamentals of HDO are of A species, and the 2nu overtone of D2O only involves A1 species, e.g., 2nu3B1 has A1 species via B1 x B1 = A1. A and A1 modes display small rhoL values which produce minima in rhoL near 2665 cm(-1) for HDO, and near 5250 cm(-1) for the D2O overtone. These minima give way to a depolarization ratio maximum when the depolarized, rhoL = 34, nu3B1 fundamental, makes its appearance in D2O at 2650 cm(-1). Fundamental and overtone depolarization ratios were used to determine the nu3B1 contribution to the depolarization ratio of the fundamental OD stretch; a value of approximately 28% resulted at 2655 cm(-1). Liquid H2O displays completely analogous features; a value of approximately 20% resulted for it at 3660 cm(-1). Nonhydrogen-bonded nu3B1, and more strongly hydrogen-bonded nu3B1, modes are also indicated for D2O and H2O. A rigorous test of the current results can be accomplished by measuring the depolarization ratio of the extraordinarily weak second Raman overtone, 3nu, recently detected for D2O.