Intrinsic product polarization and branch ratio in the S（~1D,~3P）＋HD reaction on three electronic states

The intrinsic product polarization and intramolecular isotope effect of the S（~1D,~3P） ＋ HD reaction have been investigated on both the lowest singlet state（1A） and the triplet state（3A and 3A） potential energy surfaces by using quasi-classical trajectory and quantum mechanical methods.The calculations indicate that intramolecular isotope effects are different on the three electronic states.The stereodynamics study shows that the P（θr） distributions,P（φ r） distributions,and polarization-dependent differential cross sections（PDDCSs）（00） are sensitive to mass factor and the product angular momentum vectors are not only aligned but also oriented.