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Title: Molecular beam studies of reaction dynamics

Abstract

The major thrust of this research project is to elucidate detailed dynamics of simple elementary reactions that are theoretically important and to unravel the mechanism of complex chemical reactions or photochemical processes that play important roles in many macroscopic processes. Molecular beams of reactants are used to study individual reactive encounters between molecules or to monitor photodissociation events in a collision-free environment. Most of the information is derived from measurement of the product fragment energy, angular, and state distributions. Recent activities are centered on the mechanisms of elementary chemical reactions involving oxygen atoms with unsaturated hydrocarbons, the dynamics of endothermic substitution reactions, the dependence of the chemical reactivity of electronically excited atoms on the alignment of excited orbitals, the primary photochemical processes of polyatomic molecules, intramolecular energy transfer of chemically activated and locally excited molecules, the energetics of free radicals that are important to combustion processes, the infrared-absorption spectra of carbonium ions and hydrated hydronium ions, and bond-selective photodissociation through electric excitation.

Authors:
 [1]
  1. Lawrence Berkeley Laboratory, CA (United States)
Publication Date:
Research Org.:
Brookhaven National Lab., Upton, NY (United States)
OSTI Identifier:
139901
Report Number(s):
BNL-48923; CONF-9306172-
ON: DE93015758; TRN: 93:002191-0055
Resource Type:
Conference
Resource Relation:
Conference: 15. combustion research contractors` meeting, Lake Harmony, PA (United States), 2-4 Jun 1993; Other Information: PBD: 1993; Related Information: Is Part Of Fifteenth combustion research conference; PB: 391 p.
Country of Publication:
United States
Language:
English
Subject:
40 CHEMISTRY; 66 PHYSICS; CHEMICAL REACTIONS; DYNAMICS; PHOTOCHEMICAL REACTIONS; COMBUSTION; MOLECULAR BEAMS; ENERGY TRANSFER; EXCITATION; OXYGEN; ATOM-MOLECULE COLLISIONS; ALKENES; EXCITED STATES; RADICALS; CARBONIUM COMPOUNDS; ABSORPTION SPECTROSCOPY; CATIONS; HYDROCARBONS; CARBON DIOXIDE; SULFUR DIOXIDE; SILANES; ORGANIC CHLORINE COMPOUNDS; ORGANIC BROMINE COMPOUNDS; OZONE; CHLORINE; BROMINE; DEUTERIUM; HYDROGEN; NITROGEN DIOXIDE

Citation Formats

Lee, Y.T.. Molecular beam studies of reaction dynamics. United States: N. p., 1993. Web.
Lee, Y.T.. Molecular beam studies of reaction dynamics. United States.
Lee, Y.T.. Wed . "Molecular beam studies of reaction dynamics". United States. doi:. https://www.osti.gov/servlets/purl/139901.
@article{osti_139901,
title = {Molecular beam studies of reaction dynamics},
author = {Lee, Y.T.},
abstractNote = {The major thrust of this research project is to elucidate detailed dynamics of simple elementary reactions that are theoretically important and to unravel the mechanism of complex chemical reactions or photochemical processes that play important roles in many macroscopic processes. Molecular beams of reactants are used to study individual reactive encounters between molecules or to monitor photodissociation events in a collision-free environment. Most of the information is derived from measurement of the product fragment energy, angular, and state distributions. Recent activities are centered on the mechanisms of elementary chemical reactions involving oxygen atoms with unsaturated hydrocarbons, the dynamics of endothermic substitution reactions, the dependence of the chemical reactivity of electronically excited atoms on the alignment of excited orbitals, the primary photochemical processes of polyatomic molecules, intramolecular energy transfer of chemically activated and locally excited molecules, the energetics of free radicals that are important to combustion processes, the infrared-absorption spectra of carbonium ions and hydrated hydronium ions, and bond-selective photodissociation through electric excitation.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Wed Dec 01 00:00:00 EST 1993},
month = {Wed Dec 01 00:00:00 EST 1993}
}

Conference:
Other availability
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