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首页> 外文期刊>The Journal of Chemical Physics >RESONANCE ENHANCED MULTIPHOTON IONIZATION SPECTROSCOPY OF CARBONYL SULPHIDE
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RESONANCE ENHANCED MULTIPHOTON IONIZATION SPECTROSCOPY OF CARBONYL SULPHIDE

机译:羰基硫的共振增强多光子电离光谱

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Rydberg excited states of the OCS molecule in the energy range 70500-86000 cm(-1) have been investigated via the two and three photon resonance enhancements they provide in the mass resolved multiphoton ionization (MPI) spectrum of a jet-cooled sample of the parent molecule. Spectral interpretation has been assisted by companion measurements of the kinetic energies of the photoelectrons that accompany the various MPI resonances. The present study supports the earlier conclusions of Weinkauf and Boesl [J. Chem. Phys. 98, 4459 (1993)] regarding five Rydberg origins in the 70500-73000 cm(-1) energy range, attributable to, respectively, states of (II)-I-3, (II)-I-1, (3) Delta, (1) Delta and (1) Sigma(+) symmetry arising from the 4p lambda <-- 3 pi orbital promotion. We also identify a further 21 Rydberg origins at higher energies. These partition into clumps with quantum defects ca. 3.5 and 4.5, which we associate with the orbital promotions np lambda <-- 3 pi (n = 5,6), and others with near integer quantum defect which are interpretable in terms of excitation to s,d and (possibly) f Rydberg orbitals. We also identify MPI resonances attributable to CO(X (1) Sigma(+)) fragments and to S atoms in both their ground ((3)p) and excited (D-1) electronic states. Analysis of the former resonances confirms that the CO(X) fragments resulting from one photon dissociation of OCS at excitation wavelengths ca. 230 nm are formed with a highly inverted, bimodal rotational state population distribution, whilst the latter are consistent with previous reports of the wavelength dependence for forming ground and excited state S atoms in the near uv photolysis of OCS. (C) 1996 American Institute of Physics. [References: 40]
机译:OCS分子在70500-86000 cm(-1)能量范围内的Rydberg激发态已通过其在喷射冷却的样品的质量分辨多光子电离(MPI)光谱中提供的两个和三个光子共振增强进行了研究。母体分子。伴随各种MPI共振的光电子动能的伴随测量有助于光谱解释。本研究支持Weinkauf和Boesl的早期结论。化学物理[98,4459(1993)]关于70500-73000 cm(-1)能量范围内的五个里德堡起源,分别归因于(II)-I-3,(II)-I-1,(3)状态Delta,(1)Delta和(1)Sigma(+)对称性是由4p lambda <-3 pi轨道提升引起的。我们还确定了更高能量的另外21个里德堡起源。这些被分成具有量子缺陷的团块ca。 3.5和4.5,我们将其与轨道提升np lambda <-3 pi(n = 5,6)相关联,以及其他具有接近整数量子缺陷的事物,这些缺陷可以解释为对s,d和(可能)f Rydberg的激发轨道。我们还确定了归因于CO(X(1)Sigma(+))片段和S原子的基态((3)p)和激发态(D-1)电子态的MPI共振。对前者共振的分析证实,在激发波长ca处,OCS的一个光子解离产生的CO(X)片段。 230 nm形成具有高度倒置的双峰旋转态总体分布,而后者与先前关于OCS在近紫外光解中形成基态和激发态S原子的波长依赖性的报道一致。 (C)1996年美国物理研究所。 [参考:40]

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