The photodissociation of phenol at 193 and 248 nm was studied using multimass ion-imaging techniques and step-scan time-resolved Fourier-transform spectroscopy. The major dissociation channels at 193 nm include cleavage of the OH bond, elimination of CO, and elimination of H(2)O. Only the former two channels are observed at 248 nm. The translational energy distribution shows that H-atom elimination occurs in both the electronically excited and ground states, but elimination of CO or H(2)O occurs in the electronic ground state. Rotationally resolved emission spectra of CO (1

Radical reactions: The ground-state potential energy surface of the C(2)H(5)O system is investigated by ab initio methods using optimized geometries. The rate constants for the unimolecular isomerization and decomposition reactions of the three isomeric radicals (see picture) are calculated by microcanonical transition-state theory at 200-3000 K, varying the pressures of the diluents.The ground-state potential energy surface of the C(2)H(5)O system, including the decomposition and isomerization of the ethoxy (CH(3)CH(2)O), 1-hydroxyethyl (CH(3)CHOH), and 2-hydroxyethyl (CH(2)CH(2)OH) radicals, is computed by the modified Gaussian-2 (G2M) and CCSD(T)/6-311+G(3df,2p) methods by using the geometries optimized at the B3LYP/6-311+G(3df,2p) level of theory. These detailed reaction pathways are used to calculate the rate constants for the unimolecular isomerization and decomposition reactions of the three radicals by the microcanonical transition-state theory and Rice-Ramsperger-Kassel-Marcus (RRKM) theory in the temperature range of 200-3000 K at varying pressures of He and other diluents. The predicted rate constants are in reasonable agreement with the available experimental data. In addition, the predicted heats of formation of the three isomeric radicals are compared with available experimental and theoretical values.

The rate constants for the NCN + NO reaction have been measured by laser photolysis/laser-induced fluorescence technique in the temperature range of 254-353 K in the presence of He (40-600 Torr) and N2 (30-528 Torr) buffer gases. The NCN radical was produced from the photodissociation of NCN3 at 193 nm and monitored with a dye laser at 329.01 nm. The reaction was found to be strongly positive-pressure dependent with negative-temperature dependence, as was reported previously. The experimental data could be reasonably accounted for by dual-channel Rice-Ramsperger-Kassel-Marcus calculations based on the predicted potential-energy surface using the modified Gaussian-2 method. The reaction is predicted to occur via weak intermediates, cis- and trans-NCNNO, in the 2A" state which crosses with the 2A' state containing more stable cis- and trans-NCNNO isomers. The high barriers for the fragmentation of these isomers and their trapping in the 2A' state by collisional stabilization give rise to the observed positive-pressure dependence and negative-temperature effect. The predicted energy barrier for the fragmentation of the cis-NCNNO (2A') to CN + N2O also allows us to quantitatively account for the rate constant previously measured for the reverse process CN + N2O --> NCN + NO.

An ab initio/Rice-Ramsperger-Kassel-Marcus prediction of rate constant and product branching ratios for unimolecular decomposition of propen-2-ol and related H + CH 2 COHCH 2 reaction Thermal decomposition of ethanol. III. A computational study of the kinetics and mechanism for the CH 3 + C 2 H 5 OH reactionThe kinetics and mechanism for the HϩC 2 H 5 OH reaction, a key chain-propagation step in the high temperature decomposition and combustion of ethanol, have been investigated with the modified GAUSSIAN -2 ͑G2M͒ method using the structures of the reactants, transition states and products optimized at the B3LYP/6-311ϩG(d, p) level of theory. Four transition states have been identified for the production of H 2 ϩCH 3 CHOH ͑TS1͒, H 2 ϩCH 2 CH 2 OH ͑TS2͒, H 2 ϩC 2 H 5 O ͑TS3͒, and H 2 OϩC 2 H 5 ͑TS4͒ with the corresponding barriers, 7.18, 13.30, 14.95, and 27.10 kcal/mol. The predicted rate constants and branching ratios for the three H-abstraction reactions have been calculated over the temperature range 300-3000 K using the conventional and variational transition state theory with quantum-mechanical tunneling corrections. The predicted total rate constant, k t ϭ3.15ϫ10 3 T 3.12 exp(Ϫ1508/T) cm 3 mol Ϫ1 s Ϫ1 , agrees reasonably with existing experimental data; in particular, the result at 423 K was found to agree quantitatively with an available experimental value. The small deviation between the predicted k t and another set of experimental data measured at 295-700 K has been examined by kinetic modeling; the deviation is attributable to insufficient corrections for contributions from secondary reactions.

The mechanism for the CH3+C2H5OH reaction has been investigated by the modified Gaussian-2 method based on the geometric parameters of the stationary points optimized at the B3LYP/6-311+G(d,p) level of theory. Five transition states have been identified for the production of CH4+CH3CHOH (TS1), CH4+CH3CH2O (TS2), CH4+CH2CH2OH (TS3), CH3OH+CH3CH2 (TS4), and CH3CH2OCH3+H (TS5) with the corresponding barriers 12.0, 13.2, 16.0, 44.7, and 49.9 kcal/mol, respectively. The predicted rate constants and branching ratios for the three lower-energy H-abstraction reactions were calculated using the conventional and variational transition state theory with quantum-mechanical tunneling corrections for the temperature range 300-3000 K. The predicted total rate constant, kt=8.36 x 10(-76) T(20.00) exp(5258/T) cm3 mol(-1) s(-1) (300-600 K) and 6.10 x 10(-25) T(4.10)exp(-4058/T) cm3 mol(-1) s(-1) (600-3000 K), agrees closely with existing experimental data in the temperature range 403-523 K. Similarly, the predicted rate constants for CH3+CH3CD2OH and CD3+C2H5OD are also in reasonable agreement with available low temperature kinetic data.

The unimolecular decomposition of C(6)H(5)OH on its singlet-state potential energy surface has been studied at the G2M//B3LYP/6-311G(d,p) level of theory. The result shows that the most favorable reaction channel involves the isomerization and decomposition of phenol via 2,4-cyclohexadienone and other low-lying isomers prior to the fragmentation process, producing cyclo-C(5)H(6) + CO as major products, supporting the earlier assumption of the important role of the 2,4-cyclohexadienone intermediate. The rate constant predicted by the microcanonical RRKM theory in the temperature range 800-2000 K at 1 Torr--100 atm of Ar pressure for CO production agrees very well with available experimental data in the temperature range studied. The rate constants for the production of CO and the H atom by O-H dissociation at atmospheric Ar pressure can be represented by k(CO) = 8.62 x 10(15) T(-0.61) exp(-37,300/T) s(-1) and k(H) = 1.01 x 10(71) T(-15.92) exp(-62,800/T) s(-1). The latter process is strongly P-dependent above 1000 K; its high- and low-pressure limits are given.

An analogue-oriented synthetic route for the formulation of furazan-functionalized 5-nitroimino-1,2,4-triazoles has been explored. The process was found to be straightforward, high yielding, and highly efficient, and scalable. Nine compounds were synthesized and the physicochemical and energetic properties, including density, thermal stability, and sensitivity, were investigated, as well as the energetic performance (e.g., detonation velocities and detonation pressures) as evaluated by using EXPLO5 code. Among the new materials, compounds 4-6 and 11 possess high densities, acceptable sensitivities, and good detonation performances, and thereby demonstrate the potential applications as new secondary explosives.

Twenty-one high performance monoanionic and dianionic energetic salts based on the combination of 1,2,4-triazole and 1,2,3-triazole rings were studied.