Even-odd product variation of the C(n)(+) + D(2) (n = 4-9) reaction: complexity of the linear carbon cation electronic states.

We have studied reactions between linear Cn(+) (n = 4-9) and D2, using ion mobility mass spectrometry techniques and quantum chemical calculations in order to understand the complex reactivity of the linear cluster cations. Only linear CnD(+) products were observed for the odd (n = 5, 7, 9) linear clusters, while CnD2(+) was the main product for the even clusters. For the reaction rate constants determined for these two channels, we obtained the following two features: (1) the rate constant decreases with the size n, and (2) even-sized clusters have lower rate constants than neighboring odd-sized clusters. In the theoretical calculations using the CCSD(T) and B3LYP methods with the cc-pVTZ basis, we found that a low lying (2)Σ state in odd clusters may play an important role in these reactions. This opposes the previous interpretation that the (2)Πg/u state is the dominant electronic state for linear Cn(+) (n = 4-9) clusters. We showed that a barrierless radical abstraction forming CnD(+) occurs through a direct head on approach for the (2)Σ state Cn(+). In contrast, a carbene-like insertion forming CnD2(+) occurs through a sideways approach for the (2)Πg/u state Cn(+). We have concluded that the higher rate constants for the odd clusters come from the existence of symmetry broken (2)Σ states which are absent in even linear clusters.