Lambda-doublet specificity in the low-temperature capture of NO(X 2Π1/2) in low rotational states by C+ ions

被引:6
作者
Auzinsh, M. [1 ]
Dashevskaya, E. I. [2 ,3 ]
Litvin, I. [2 ,3 ]
Nikitin, E. E. [2 ,3 ]
Troe, J. [3 ,4 ]
机构
[1] Latvian State Univ, Dept Phys, LV-1586 Riga, Latvia
[2] Technion Israel Inst Technol, Schulich Fac Chem, IL-32000 Haifa, Israel
[3] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[4] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
关键词
carbon; electron capture; hyperfine structure; nitrogen compounds; positive ions; reaction rate constants; rotational states; Stark effect; DIPOLAR MOLECULES; CHANNEL TREATMENT; REACTION-RATES; NITRIC-OXIDE; LOW-ENERGY; SPECTRUM; COLLISIONS; BAND;
D O I
10.1063/1.3043365
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Following our general approach to Lambda-doubling specificity in the capture of dipolar molecules by ions [M. Auzinsh , J. Chem. Phys. 128, 184304 (2008)], we calculate the rate coefficients for the title process in the temperature range 10(-4)< T < 10(2) K. Three regimes considered are as follows: (i) nonadiabatic capture in the regime of high-field Stark effect with respect to the Lambda-doubling components, (10(-1)< T < 10(2) K), (ii) adiabatic capture in the regime of intermediate Stark effect (10(-3)< T < 10(-1) K), and (iii) adiabatic capture in the limit of very low temperatures (T < 10(-3) K) in the regime of quadratic Stark effect with respect to the Lambda-doubling and hyperfine components. The results predict a high specificity of the capture rates with respect to the Lambda-doublet states even under conditions when the collision energy of the partners strongly exceeds the Lambda-doubling splitting.
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页数:10
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