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Adiabaticity of potential surfaces in elementary reactions

Adiabaticity of potential surfaces in elementary reactions
基元反应中势表面的绝热性
批准号:
04453012
负责人:
MATSUMI Yutaka
金额:
$4.61万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1992
资助国家:
日本
项目状态:
已结题
起止时间:
1992 至 1993

项目摘要

项目成果

MATSUMI Yutaka的其他基金

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中文摘要
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英文摘要
1. Adiabaticity of potential surface in photodissociation processesAtomic fragments produced in the photodissociation processes of molecules were detected with a laser multi-photon ionization technique and also with a laser-induced fluorescence technique. The non-adiabtic transitions between potential curves during the bnd break-up in the dissociation processes were investigated, which affect the electronic and translational states of the fragment atoms. The photodissociation processes of Cl_2, ICl, H_3O_2, SiH_4, Ethylene chlorides, and O_3 were studied.2. Adiabaticity of potential surfaces in reaction processesReactions of active atomic species, O(2P^<4\1>D), S(3P^<4\1>D), H(ls ^2S) and Xe(6p) with other molecules by collisions were investigated by observing the nascent translational and internal states of the reaction products. Since the photodissociation processes were used as sources of the active atom reactants and the products states were studied under single collision energies could be defined and angular distribution of the product velocities could be measured. The translational energies of the reaction products were calculated from the measured Doppler profiles. By measuring the fine structure branching ratios of product atoms and ro-vibronic states of product molecules, the adiabaticity of the potential curves in the reactions were investigated. The following reactions were studied, (1) O(^1D) + H_2, D_3 and HD, (2) O(^1D) + alkanes, (3) O(^1D) + CH_3OH, (4) SO(^1D) + H_2D_2 and HD, (5) S(^1D) + thiirane, (6) Ze(6p) + H_2 and HD, and (7) Xe(6p) + H_2O.
期刊论文(98)
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会议论文
Yuxiang Mo: "Mechanism of the UV photodissociation of chloroethylenes determined from the Doppler profiles,spatial anisotropy,and power dependence of the photofragments" J.Chem.Phys.97. 4815-4826 (1992)
莫宇翔:“从多普勒分布、空间各向异性和光碎片的功率依赖性确定氯乙烯的紫外光解离机制”J.Chem.Phys.97。
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发表时间:
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作者: []
通讯作者:
Satoshi Hashimoto: "OH(A^2Σ^+)fragment emission from reaction of electronically excited Xe(6p)with H_2O under free jet and bulb conditions" Chem.Phys.Lett.200. 624-630 (1992)
Satoshi Hashimoto:“自由射流和灯泡条件下电子激发 Xe(6p) 与 H_2O 反应的 OH(A^2Σ^+) 碎片发射”Chem.Phys.Lett.200 (1992)。
DOI: --
发表时间:
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作者: []
通讯作者:
S.M.Shamsuddin: "O(^3P_<jA>) atom formation from photodissociation of ozoneat visible and ultraviolet region" Can. J.Chem.in press. (1994)
S.M.Shamsuddin:“可见光和紫外线区域臭氧光解形成 O(^3P_<jA>) 原子”。
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作者: []
通讯作者:
Yutaka Matsumi: "Fine structure branching ratios and translational energies of O(^3P_j) atoms produced from collision induced intersystem cross of O(^1D) atoms" J.Chem. Phys.100. 315-324 (1994)
Yutaka Matsumi:“碰撞诱导 O(^1D) 原子的系间交叉产生的 O(^3P_j) 原子的精细结构分支比和平移能”J.Chem。
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作者: []
通讯作者:
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