On the meaning of “collision rate constants” for ion-molecule reactions: Association of hydrogen atoms with C6H5+ and small alkyl radicals with C7H7+ ions

• Published in: International journal of mass spectrometry Vol. 458; p. 116455
• Main Authors: Ard, S.G., Cobos, C.J., Maergoiz, A.I., Shuman, N.S., Troe, J., Viggiano, A.A.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.12.2020
• ISSN: 1387-3806; 1873-2798
• DOI: 10.1016/j.ijms.2020.116455

Limiting high pressure rate constants for the association of H with C6H5+ and of CH3, C2H5, and n-C3H7 radicals with C7H7+ molecular ions are analyzed in terms of “rigidity factors” arising from the anisotropy of the interaction potentials and “collision rate constants” in the absence of anisotropy (the latter corresponding to phase space theory, PST). Model calculations based on ab initio potential energy surfaces show that the PST rate constants kPST(T) exceed collision rate constants from conventional ion-molecule capture theory (in this case given by Langevin rate constants kL). They can be represented by kPST(T) = kL + kh.sph. where kh.sph. denotes hard-sphere collision numbers with collision radii r0. The r0 derived from the modelled kPST(T) are related to properties of the interaction potentials. Applications to other ion-molecule reactions are proposed. [Display omitted] •Collision rate constants.•Ion-molecule reactions.•Physe space theory.