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首页> 外文期刊>Journal of Molecular Spectroscopy >THE TORSION-INVERSION ENERGY LEVELS IN THE S-1(N,PI-ASTERISK) ELECTRONIC STATE OF ACETALDEHYDE FROM HIGH-RESOLUTION JET-COOLED FLUORESCENCE EXCITATION SPECTROSCOPY
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THE TORSION-INVERSION ENERGY LEVELS IN THE S-1(N,PI-ASTERISK) ELECTRONIC STATE OF ACETALDEHYDE FROM HIGH-RESOLUTION JET-COOLED FLUORESCENCE EXCITATION SPECTROSCOPY

机译:高分辨率射流冷却荧光激发光谱中S-1(N,PI-ASTERISK)电子态的扭转-反能能级

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摘要

The laser-induced fluorescence excitation spectrum (LIF) of acetaldehyde that results from the emission from the S-1(n, pi*) electronic state has been observed under very high resolution with a CW pulse-amplified laser under jet-cooled conditions. The origins of seven bands were determined by rotational analyses with a rigid-rotor Hamiltonian. The origins were fitted to a set of levels that were obtained from a Hamiltonian that employed flexible torsion-wagging large amplitude coordinates. The potential surface derived from the fitting procedure yielded barriers to torsion and inversion of 721.43 and 585.13 cm(-1), respectively. Minima in the potential hypersurface at theta = 58.6 degrees and alpha = 35.7 degrees defined the corresponding equilibrium positions for the torsion and wagging coordinates. (C) 1996 Academic Press, Inc. [References: 31]
机译:在CW脉冲放大激光器的射流冷却条件下,已在非常高分辨率下观察到了由S-1(n,pi *)电子态发射产生的乙醛的激光诱导的乙醛的荧光激发光谱(LIF)。通过使用刚性转子​​哈密顿量的旋转分析确定了七个带的起源。将原点拟合到一组水平,这些水平是从采用挠性扭摆大振幅坐标的哈密顿量获得的。从拟合过程中得出的潜在表面分别产生了721.43和585.13 cm(-1)的扭转和反转障碍。在θ= 58.6度和α= 35.7度处,潜在超曲面的最小值定义了扭转和摆动坐标的相应平衡位置。 (C)1996 Academic Press,Inc. [参考:31]

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