h2co旋转光谱中的磁性超精细结构

H. Takuma
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引用次数: 21

摘要

讨论了1 Σ状态下c2v对称不对称转子分子的磁超细相互作用理论,并利用束激射器研究了甲醛低频旋转谱中的磁超细结构。在J =4, K -1 =3和J =5, K -1 =3的Q分支跃迁中,Δ F =0和Δ F =±1分量具有良好的信噪比。J =5, K -1 =3线中Δ F =0分量的频率为18.275±0.004 Mc。对观察到的超细结构进行了理论分析,确定了超细耦合常数为α=-13.2±3.4 kc, β=-3.0±3.4 kc和γ=30.2±2.7 kc,并对超细耦合常数进行了理论解释,发现了超细耦合常数与不对称转子分子的旋转g因子成正比关系。通过对这两个量的比较,得到h2o中质子周围的a v = 1.5×10 24 cm -3。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnetic Hyperfine Structure in the Rotational Spectrum of H 2 CO
The theory of magnetic hyperfine interaction of an asymmetric rotor molecule with C 2 v symmetry in 1 Σ state was discussed, and the magnetic hyperfine structures in the low frequency rotational spectrum of formalde-hyde were studied with a beam maser. The Δ F =0 and the Δ F =±1 components in the J =4, K -1 =3 and the J =5, K -1 =3 Q -branch transitions were observed with good signal-to-noise ratio. The frequency of the Δ F =0 component of the J =5, K -1 =3 line was measured as 18.275±0.004 Mc. The observed hyperfine structures were analysed with the theory, and the hyperfine coupling constants were determined as α=-13.2±3.4 kc, β=-3.0±3.4 kc and γ=30.2±2.7 kc. The coupling constants were theoretically interpreted, and a proportionality of the hyperfine coupling constans and the rotational g factors for the asymmetric rotor molecule was found. a v arround the proton in H 2 CO was obtained as 1.5×10 24 cm -3 from the comparison of these two quantities.
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