UNIMOLECULAR DISSOCIATION IN ALLENE AND PROPYNE - THE EFFECT OF ISOMERIZATION ON THE LOW-PRESSURE RATE

The unimolecular dissociation of the C3H4 isomers allene and propyne h as been examined using two complementary shock-tube techniques: laser schlieren (LS) and time-of-flight (TOF) mass spectrometry. The LS expe riments cover 1800-2500 K and 70-650 Torr, in 1, 2, and 4% propyne/Kr and 1 and 2% allene/Kr, whereas the TOF results extend from 1770 and 2 081 K in 3% allene or propyne in Ne. The possible channels for unimole cular dissociation in the C3H4 system of isomers are considered in det ail, using new density functional theory calculations of the barriers for insertion of several C3H2 into H-2 to evaluate the possibility of Hz elimination as a dissociation route. The dominant path clearly rema ins CH fission, from either isomer, as suggested in earlier work, alth ough some small amount of H-2 elimination may be possible from allene. Rate constants for the CH fission of both allene and propyne were obt ained by the usual model-assisted extrapolation of LS profiles to zero time using an extensive mechanism constructed to be consistent with b oth the time variation of LS gradients and the TOF product profiles. T his procedure then provides rate constants effectively independent of both the near-thermoneutral isomerization of the allene/propyne and of secondary chain reactions. Derived rate constants show a strong, pers istent pressure dependence, i.e., a quite unexpected deviation (fallof f) from second-order behavior. These rate constants are nearer first t han second order even for T > 2000 K. They are also anomalously large; RRKM rates using literature barriers and routine energy-transfer para meters are almost an order of magnitude too slow. The two isomers show slightly differing rates, and falloff is slightly less in allene. It is suggested that isomerization is probably slow enough for this diffe rence to be real. The anomalously large rates and falloff are both con sistent with an unusually large low-pressure-limit rate in this system . Extensive isomerization of these C3H4 is possible for energies well below their CH fission barriers, and this can become hindered internal rotation in the activated molecule. On the C3H4 surface we identify t hree such accessible rotors. State densities for the molecule includin g these rotors are calculated using a previous general classical formu lation. Insertion of these state densities into the RRKM model results in rates quite close to the measured magnitudes, and showing much of the observed falloff. The increase in the low-pressure rate is as much as a factor of 8; a necessary but nonetheless remarkable effect of an harmonicity on the unimolecular rate. This again demonstrates the impo rtance of accessible isomerization and consequent hindered internal ro tation on the rate of dissociation of unsaturated species.