PUB - Publikationen an der Universität Bielefeld

Ion/molecule reactions of two series of isomeric graphitic carbon/hydrogen cluster ions CnHx+, n = 18,20; x = 4-12, in the gas phase with benzene and benzene-d(6), have been studied by using Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry. The cluster ions CnHx+ have been generated by consecutively removing H atoms from the four ionized polycyclic aromatic hydrocarbon (PAH) C18H12 isomers triphenylene 1, chrysene 2, 1,2-benzanthracene 3 and 2,3-benzanthracene 4, and from the two C20H12 isomers perylene 5 and benzo[e]pyrene 6. For the removal of H atoms, the method of sustained off-resonance irradiation collision-induced dissociation (SORI-CID) in FT-ICR has been applied. Consistent with our previous studies of ions C18Hx+, the ions C20Hx+ differ in their reactions from the ions formed by laser evaporation of graphite as reported by Bowers and coworkers and retain very likely the graphitic carbon skeletons of the original PAHs. The ion/molecule reaction products, the reaction channels and their branching ratios, the bimolecular rate constants k(bi) and the SORI-CID fragments of the product ions provide valuable information about the reactivity and structure of the cluster ions CnHx+. The dependence of the bimolecular rate constants k(bi) on the structures of the isomeric parent PAHs indicates that the ions CnHx+ "remember" the skeleton of their precursor PAH. Two kinds of reactions are observed, an addition of a benzene molecule probably by a strained triple aryne bond as in the carbon cluster ion CnHx+ (aryne reactivity) and an addition of a benzene molecule followed by H elimination which can be attributed to a carbenium-like reactivity (C+ reactivity). Then there are unreactive components of the isomeric cluster ions CnHx+, x = 4-9, which represent the non-reactivity. For the whole series of the cluster ions C18Hx+ and C20Hx+ the relative importance of these reactivities and the corresponding rate constants k(bi) with benzene alternates with the odd- and even numbers of H atoms indicating their structural features and the preferable formation of aryne bonds especially in the cluster ions CnHx+ containing a small number of hydrogen atoms. SORI-CID studies of the product ions [CnHx.C6X6](+) (X = H or D) or [CnHx. (C6H6)(2)](+) support the operation of a Diels-Alder mechanism in the addition process of both reactive channels, in which a triple aryne bond behaves as a dienophile toward benzene. The ion/molecule reactions with benzene can be considered as a useful probe of the structures of the studied cluster ions CnHx+.