Crossed‐molecular‐beams investigation of the excitation of ground‐state neon atoms by 4.6‐eV helium metastables

1976 ◽  
Vol 47 (3) ◽  
pp. 1062-1064 ◽  
Author(s):  
E. L. Leasure ◽  
C. R. Mueller
Keyword(s):  
Ground State ◽  
Molecular Beams ◽  
Crossed Molecular Beams

Combined Crossed Molecular Beams and Ab Initio Study of the Bimolecular Reaction of Ground State Atomic Silicon (Si; 3P) with Germane (GeH4; X1A1)

ChemPhysChem ◽  
2021 ◽  
Author(s):  
Alexander Mebel ◽  
Vladislav S. Krasnoukhov ◽  
Valeriy N. Azyazov ◽  
Srinivas Doddipatla ◽  
Zhenghai Yang ◽  
...  
Keyword(s):  
Ab Initio ◽  
Ground State ◽  
Molecular Beams ◽  
Bimolecular Reaction ◽  
Ab Initio Study ◽  
Crossed Molecular Beams

scholarly journals Imaging H abstraction dynamics in crossed molecular beams: O(3P) + propanol isomers

2019 ◽  
Vol 21 (26) ◽  
pp. 14186-14194 ◽  
Author(s):  
Hongwei Li ◽  
Alexander Kamasah ◽  
Arthur G. Suits
Keyword(s):  
Transition State ◽  
Long Range ◽  
Ground State ◽  
Molecular Beams ◽  
Dipole Interaction ◽  
Bimolecular Reaction ◽  
Crossed Molecular Beams

Direct rebound dynamics are revealed for bimolecular reaction of the ground state O(3P) atom with propanol isomers, involving the post transition state long-range dipole–dipole interaction between the dipolar OH and hydroxypropyl radicals.

A crossed molecular beams investigation of the reactions of atomic silicon (Si(3P)) with C4H6 isomers (1,3-butadiene, 1,2-butadiene, and 1-butyne)

2019 ◽  
Vol 520 ◽  
pp. 70-80
Author(s):  
Aaron M. Thomas ◽  
Beni B. Dangi ◽  
Tao Yang ◽  
Ralf I. Kaiser ◽  
Bing-Jian Sun ◽  
...  
Keyword(s):  
Molecular Beams ◽  
Crossed Molecular Beams

Crossed Molecular Beams Studies of Phenyl Radical Reactions with Propene and trans-2-Butene

2013 ◽  
Vol 117 (51) ◽  
pp. 13967-13975 ◽  
Author(s):  
Daniel R. Albert ◽  
Michael A. Todt ◽  
H. Floyd Davis
Keyword(s):  
Molecular Beams ◽  
Radical Reactions ◽  
Phenyl Radical ◽  
Crossed Molecular Beams

The dynamics of the reaction of O(1D) with HBr studied by crossed molecular beams and time-resolved Fourier transform spectroscopy

1994 ◽  
Vol 72 (3) ◽  
pp. 888-902 ◽  
Author(s):  
N. Balucani ◽  
L. Beneventi ◽  
P. Casavecchia ◽  
G. G. Volpi ◽  
E. J. Kruus ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Large Fraction ◽  
Branching Ratio ◽  
Molecular Beams ◽  
Momentum Conservation ◽  
Fourier Transform Spectroscopy ◽  
Fast Time ◽  
Time Resolved ◽  
Vibrational Distribution ◽  
Crossed Molecular Beams

The reaction O(1D) + HBr has been investigated by the crossed molecular beams and infrared chemiluminescence methods in an effort to characterize the dynamics of both possible reactive channels. The angular and velocity distribution of the BrO product from the O(1D) + HBr → BrO + H pathway have been obtained in crossed beam experiments at collision energies, Ec, of 5.0 and 14.0 kcal/mol. The product center-of-mass angular distribution is found to be almost backward–forward symmetric at both Ec, with backward scattering being slightly favored, from which it is deduced that two processes contribute to this channel: a dominant one occurring via formation of a long-lived complex, following O(1D) insertion, and another one occurring via direct abstraction of the halogen atom and giving rise to a rebound dynamics. The large fraction (≈50%) of available energy released into translation indicates the existence of a potential barrier for H-displacement in the exit channel. From energy and angular momentum conservation arguments, it is inferred that BrO is formed rotationally very hot in the lowest vibrational levels of both 2Π3/2 and 2Π1/2 electronic states. The initial vibrational distribution of the OH product from the O(1D) + HBr → OH + Br channel has been measured using fast time-resolved Fourier transform spectroscopy. The vibrational distribution is strongly inverted, from which it is deduced that the HOBr intermediate dissociates very rapidly, before energy randomization occurs. A lower limit to the branching ratio of the relative cross sections for the BrO + H and OH + Br channels is derived (σ(BrO + H)/σ(OH + Br) ≥ 0.16 ± 0.07) and compared to recent bulk work. The dynamical results for the overall reaction are discussed with reference to the relevant singlet and triplet potential energy surfaces and possible molecular configurations involved. Comparison with the dynamics of the ground state reaction O(3P) + HBr → OH + Br is carried out also, to examine the effect of electronic excitation on the dynamics of the reactions of atomic oxygen with hydrogen halides.

Angle-energy distributions of Penning ions in crossed molecular beams. IV. He*(2 1S,2 3S)+H2→He+H2++e−

2004 ◽  
Vol 120 (18) ◽  
pp. 8485-8493 ◽  
Author(s):  
Keerti Gulati ◽  
Elizabeth J. Longley ◽  
Michael J. Dorko ◽  
Kyle L. Bittinger ◽  
P. E. Siska
Keyword(s):  
Molecular Beams ◽  
Energy Distributions ◽  
Crossed Molecular Beams

Crossed molecular beams studies of the reactions of uranium with selected oxidizers

1980 ◽  
Vol 69 (2) ◽  
pp. 301-304 ◽  
Author(s):  
Neil C. Lang ◽  
Richard C. Stern ◽  
Michael G. Finley
Keyword(s):  
Molecular Beams ◽  
Crossed Molecular Beams
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