St. Arnold et al., RATE CONSTANTS AND BRANCHING RATIOS FOR THE REACTIONS OF SELECTED ATMOSPHERIC PRIMARY CATIONS WITH N-OCTANE AND ISOOCTANE (2,2,4-TRIMETHYLPENTANE), The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 101(49), 1997, pp. 9351-9358
Gas-phase ion molecule reactions of the primary atmospheric cations (N
O+, O-2(+), O+, N+, and N-2(+)) With two isomers of octane, n-C8H18 an
d iso-C8H18 (2,2,4-trimethylpentane) have been studied using a variabl
e temperature selected ion flow tube instrument. Reaction rate constan
ts and product branching fractions were measured from 300 to 500 K. Th
e reactions of O-2(+), O+, N+, and N-2(+) with n-C8H18 and iso-C8H18 p
roceed at the collision rate via dissociative and/or nondissociative c
harge transfer. The NO+ reactions occur primarily by hydride transfer;
the reaction rate for the straight-chain isomer is only one-fourth th
e collision rate, while the reaction rate for the branched isomer is s
ignificantly enhanced. The reaction of n-octane with each atmospheric
cation generates two to four major product ions and numerous minor spe
cies. The major ionic products are alkyl cations, CnH2n+1+, where the
degree of fragmentation of the hydrocarbon chain is governed largely b
y the reactant ion recombination energy. The largest ionic products ob
served, n-C8H17+ and n-C8H18+ thermally decompose at temperatures abov
e 300 K. The reaction of isooctane with each atmospheric cation genera
tes fewer minor species than was observed in the n-octane reactions, a
nd only one to three major product ions are observed. The main ionic p
roduct of the O-2(+), O+, N+, and N-2(+) reactions is the alkyl cation
C4H9+, although several reactions also produce significant amounts of
the related radical cation C4H8+. The main ionic product of the NO+ r
eaction, C8H17+, thermally decomposes into C4H9+ at temperatures above
300 K. Presumably, the specificity of the product ion formation in th
e iso-C8H18 reactions is a consequence of the neutral reactant structu
re. Except for thermal fragmentation of C8Hm+ product ions at temperat
ures above 300 K, there is little temperature dependence on the produc
t ion branching fractions for the reported reactions.