Arrhenius activation parameters (Ea and A) for the loss of neutral nucleobase from a series of doubly deprotonated oligodexoynucleotide 10-mers of the type XT9, T9X, and T5XT4, where X=A, C, and G, have been determined using the blackbody infrared radiative dissociation technique. At temperatures of 120 to 190 °C, the anions dissociate exclusively by the loss of a neutral nucleobase (XH), followed by cleavage of the sugar 3′ C-O bond leading to (a-XH) and w type ions or, in the case of the T9X2− ions, the loss of H2O. The dissociation kinetics and energetics are sensitive to the nature and position of X. Over the temperature range investigated, the kinetics for the loss of AH and GH were similar, but ∼100 times faster than for the loss of CH. For the loss of AH and GH, the values of Ea are sensitive to the position of the base. The order of the Eas for the loss of XH from the 5′ and 3′ termini is: C>G>A; while for T5XT4 the order is: C>A>G. The trends in the values of Ea do not parallel the trend in deprotonation enthalpies or proton affinities of the nucleobases in the gas phase, indicating that the energetic differences do not simply reflect differences in their gas phase acidity or basicity. The pre-exponential factors (A) vary from 1010 to 1015 s−1, depending on the nature and position of X. These results suggest that the reactivity of individual nucleobases is influenced by stabilizing intramolecular interactions.