Vibrational excitation of OH(X2Π) produced in the reaction of O(1D) with H2
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[1] A. Ravishankara,et al. O3 photolysis at 248 nm and O(1D2) quenching by H2O, CH4, H2, and N2O: O(3PJ) yields , 1982 .
[2] D. Donaldson,et al. Detailed energy partitioning in the decomposition of chemically energized C2H3F , 1982 .
[3] P. Whitlock,et al. Quasiclassical trajectory investigation of the reaction O( 1D)+H2 , 1982 .
[4] S. Sibener,et al. REACTIVE SCATTERING OF O(1D) + H2 , 1981 .
[5] T. Kleindienst,et al. The reaction of hydrogen atoms with ozone as a source of vibrationally excited OH(X 2πi)v = 9 for kinetic studies , 1981 .
[6] George C. Schatz,et al. A quasiclassical trajectory study of reagent vibrational excitation effects in the OH+H2→H2O+H reaction , 1981 .
[7] R. A. Cox,et al. Evaluated kinetic and photochemical data for atmospheric chemistry: Volume III - gas phase reactions of inorganic halogens , 2006 .
[8] J. Butler,et al. OH (X 2Πi) product internal energy distribution formed in the reaction of O(1D2) with H2 , 1980 .
[9] J. Wiesenfeld,et al. Direct observation of O(3PJ) in the photolysis of O3 at 248 nm , 1980 .
[10] K. Shobatake,et al. Ozone photolysis: A determination of the electronic and vibrational state distributions of primary products , 1980 .
[11] A. D. McLean,et al. Extended basis first‐order CI study of the 1A′, 3A″, 1A″, and B̃ 1A′ potential energy surfaces of the O(3P,1D)+H2(1Σg+) reaction , 1979 .
[12] J. Butler,et al. The OH(X2Π, υ = 0) rotational energy distribution in the reaction of O(1D) + H2 , 1979 .
[13] W. Lester,et al. Product state distributions in the reaction O(1D2)+H2→OH+H: Comparison of experiment with theory , 1979 .
[14] L. F. Keyser. Absolute rate constant and temperature dependence of the reaction between hydrogen (2S) atoms and ozone , 1979 .
[15] A. Ravishankara,et al. Absolute rate constant for the reaction OH (v=0)+O3→HO2 +O2 over the temperature range 238–357 °K , 1979 .
[16] P. Fairchild,et al. Relative quantum yields of O(1D) in Ozone Photolysis in the region between 250 and 300 nm , 1978 .
[17] R. Macdonald,et al. The microscopic reaction dynamics and branching ratio in the F + HCOOH and F + H2CO reactions☆ , 1978 .
[18] J. Michael,et al. Absolute rate of the reaction of hydrogen atoms with ozone from 219–360 K , 1978 .
[19] D. Robinson,et al. A pure‐rotational collisionally pumped OH laser , 1977 .
[20] M. Clyne,et al. Atomic resonance fluorescence for rate constants of rapid bimolecular reactions. Part 5—Hydrogen atom reactions; H + NO2 and H + O3 , 1977 .
[21] K. Sorbie,et al. Theoretical study of the O(D) + H2(Sg ) reactive quenching process , 1976 .
[22] Harold S. Johnston,et al. Reactions and quenching of vibrationally excited hydroxyl radicals , 1976 .
[23] F. Mies. Calculated vibrational transition probabilities of OH(X2Π) , 1974 .
[24] D. Husain,et al. Electronically excited oxygen atoms, O(21D2). A time‐resolved study of the collisional quenching by the gases H2, D2, CH4, NO, NO2, N2O, and C3O2 using atomic absorption spectroscopy in the vacuum ultraviolet , 1973 .
[25] K. Welge,et al. Photodissociation of O3 in the Hartley Band. Reactions of O(1D) and O2(1Σg+) with O3 and O2 , 1971 .
[26] A. Potter,et al. Reaction rate of vibrationally excited hydroxyl with ozone. , 1971, Applied optics.
[27] H. Bergh,et al. An hydroxyl radical infrared laser , 1971 .
[28] L. F. Phillips,et al. Mass Spectrometric Studies of Atomic Reactions. III. Reactions of Hydrogen Atoms with Nitrogen Dioxide and with Ozone , 1962 .
[29] R. Norrish,et al. The production of vibrationally excited hydroxyl radicals under isothermal conditions by flash photolysis , 1961, Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences.
[30] R. Norrish,et al. VIBRATIONAL DISEQUILIBRIUM IN REACTIONS BETWEEN ATOMS AND MOLECULES , 1960 .