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Vibrational autoionization of state-selective jet-cooled methanethiol (CH3SH) investigated with infrared plus vacuum-ultraviolet photoionization

机译:用红外线加上真空 - 紫外线离子化研究的状态选择性喷射冷却甲醇(CH3SH)的振动自动化

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摘要

Vibrational autoionization of Rydberg states provides key information about nonadiabatic processes above an ionization threshold. We employed time-of-flight mass detection of CH3SH+ to record vibrational-state selective photo-ionization efficiency (PIE) spectra of jet-cooled methanethiol (CH3SH) on exciting CH3SH to a specific vibrationally excited state with an infrared (IR) laser, followed by excitation with a tunable laser in the vacuum-ultraviolet (VUV) region for ionization. Autoionizing Rydberg states assigned to the ns, np, nd and nf series are identified. When IR light at 2601 (nu(3), SH stretching mode) and 2948 cm(-1) (nu(2), CH3 symmetric stretching mode) was employed, the Rydberg series converged to the respective vibrationally excited (nu(3) and nu(2)) states of CH3SH+. When IR light at 3014 cm(-1) (overlapped nu(1)/nu(9), CH3 antisymmetric stretching and CH2 antisymmetric stretching modes) was employed, Rydberg series converging to two vibrationally excited states (nu(1) and nu(9)) of CH3SH+ were observed. When IR light at 2867 cm(-1) (2 nu(10), overtone of CH3 deformation mode) and 2892 cm(-1) (2 nu(4), overtone of CH2 scissoring mode) was employed, both Delta nu = 01 and Delta nu = -2 ionization transitions were observed; there is evidence for direct ionization from the initial state into the CH3SH+ (nu(+)(4) = 1) continuum. In all observed IR-VUV-PIE spectra, the ns and nd series show intensity greater than the other Rydberg series, which is consistent with the fact that the highest-occupied molecular orbital of CH3SH is a p-like lone pair orbital on the S atom. The quantum yields for autoionization of various vibrational excited states are discussed. Values of nu(1) = 3035, nu(2) = 2884, nu(3) = 2514, and nu(9) = 2936 cm(-1) for CH3SH+ derived from the converged limits agree satisfactorily with values observed for Ar-tagged CH3SH+ at 3026, 2879, 2502, and 2933 cm(-1).
机译:Rydberg状态的振动自动化提供有关离电离阈值之上的非等处理的关键信息。我们采用CH3SH +的飞行时间谱系检测,以记录喷射甲基硫醇(CH3SH)的振动状态选择性光电电离效率(CH3SH)的振动状态选择性光电电离效率(CH3SH),以具有红外(IR)激光的特定振动激发状态,然后用可调谐激光激发真空 - 紫外(VUV)区域进行电离。识别了分配给NS,NP,ND和NF系列的自动化Rydberg状态。当采用2601(NU(3),SH拉伸模式)和2948厘米(-1)(NU(2),CH3对称拉伸模式)时,Rydberg系列融合到相应的振动激发(NU(3)和nu(2))CH3SH +的州。当采用3014厘米(-1)(重叠的Nu(1)/ Nu(9),CH3反对称拉伸和CH2反对称拉伸模式时,Rydberg系会聚到两个振动激发态(Nu(1)和Nu(观察到CH3SH + 9)。当使用2867厘米(-1)(2元(10),CH3变形模式的泛音)和2892cm(-1)(2 nu(4),CH2剪刀模式的泛音)时,Δnu =观察到01和Delta nu = -2电离转变;有证据表明从初始状态直接电离到CH3SH +(NU(+)(4)= 1)连续体内。在所有观察到的IR-Vuv-饼谱谱中,NS和ND系列的强度大于其他Rydberg系列,这与CH3SH的最高分子轨道的含量是S的最高分子轨道的事实一致原子。讨论了各种振动激发态的自动化的量子产率。 nu(1)= 3035,nu(2)= 2884,nu(3)= 2514,nu(3)= 2514,nu(9)= 2936cm(-1)用于汇聚限制的Ch3sh +令人满意地观察到AR-标记的CH3SH +在3026,2879,2502和2933厘米(-1)。

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