硝基甲烷团簇在氧k边的内壳激发和破碎

K. Tabayashi, T. Yamanaka, H. Namatame, M. Taniguchi
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引用次数: 2

摘要

研究了硝基甲烷(NM)团簇在氧k边区的激发光谱和团束的破碎。除了质子化团簇(NM)n·H+外,我们还在飞行时间光谱中发现了一系列混合碎片团簇阳离子[(NM)n·X+, (X = CH3, NO, NO2)]的产生。通过监测来自团簇的碎片的部分离子产额光谱,可以在没有自由分子贡献的情况下产生“团簇特异性”激发光谱。“团簇特异性”带与“单体”带的比较表明,团簇的第一共振${\rm O}1s \到\pi^*_{\rm NO}$带向高能移动了~ 0.1 eV。反键态的核激发谱与理论预测相符。第一个${\rm O}1s到\pi ^*_{\rm NO}$的带移解释为聚类时形成的弱氢键相互作用。核激发纳米簇的破碎机制…
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INNER-SHELL EXCITATION AND FRAGMENTATION OF NITROMETHANE CLUSTERS AT THE OXYGEN K-EDGE
Inner-shell excitation spectra and fragmentation of nitromethane (NM) clusters have been studied in the oxygen K-edge region under cluster beam conditions. Besides the protonated clusters (NM)n · H+, we identified the production of series of mixed fragment-cluster cations, [(NM)n · X+, (X = CH3, NO, NO2)] in time-of-flight spectra of the NM clusters. "Cluster-specific" excitation spectra could be generated without contribution of free molecules by monitoring partial-ion-yield spectra of the fragments originating from the clusters. Comparison of the "cluster-specific" band with "monomer" band revealed that the first resonance ${\rm O}1s \to \pi^*_{\rm NO}$ band of clusters shifts to a high energy by ~ 0.1 eV. The core-excitation spectrum to the antibonding state compared well with theoretical prediction. The band-shift of the first ${\rm O}1s \to \pi ^*_{\rm NO}$ was interpreted as being due to the weak hydrogen-bond interaction formed upon clustering. Fragmentation mechanism of the core-excited NM cluster...
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