Kinetics of radiative/termolecular associations in the low pressure regime: reactions of bare Au+ with benzene

Consecutive ion/molecule reactions of gold cation Au+ with (deuternted) ben zene are examined by Fourier-transform mass spectrometry. Primary products upon reacting Au+ with C6H6 are due to charge transfer to afford C6H6+. con comitant with neutral gold as well as ligand association to yield the Au(C6 H6)(+) complex. Subsequent reactions of so-formed Au(C6H6)(+) with benzene result in exclusive formation of the corresponding bisligated complex Au(C6 H6)(2)(+). In contrast to a previous report by Ho and Dunbar [Int. J. Mass Spectrom. 182/183 (1999) 175], occurrence of charge transfer from benzene t o Au(C6H6)(+) affording C6H6+. concomitant with neutral Au(C6H6) is rigorou sly excluded. Our results are supported by ab initio calculations which pre dict a strong interaction in the Au(C6H6)(+) cation, whereas neutral Au(C6H 6) is best described as a loose van der Waals complex: i.e. D-0(Au+-C6H6) = 61.1 kcal/mol versus D-0(Au-C6H6) = 2.0 kcal/mol. Interestingly, the react ion kinetics for the sequential additions of benzene to cationic gold show irregularities which point to a non-negligible role of excess energy in con secutive bimolecular associations at low pressures. (C) 2000 Elsevier Scien ce B.V.