Double resonance techniques for high resolution spectroscopy of unstable molecules

W. Ernst
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Abstract

Free radicals often exhibit complex optical spectra. Dopplerfree laser spectroscopy is the appropriate tool in many cases, but its limitations may be reached already when the fine and hyperfine structure of a heavy diatomic is to be analyzed. Double resonance techniques help to simplify dense spectra and to assign lines. If microwave radiation is used in addition to a single frequency laser, small energy splittings in individual electronic states can be investigated independently. The recently developed microwave optical polarization spectroscopy (MOPS)1 has proved to offer the necessary high resolution and the sensitivity needed to study chemically unstable species at low concentrations. If a beam of the species can be produced, ground state level splittings and shifts in external fields can be measured with 10-kHz accuracy by using the molecular beam laser-microwave double resonance technique.2 The power of these methods has been demonstrated in applications to alkaline earth monohalide radicals. Local perturbations in excited states were revealed and details of the electronic structure could be derived from hyperfine structure and Stark effect measurements.
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不稳定分子高分辨光谱的双共振技术
自由基通常表现出复杂的光谱。在许多情况下,无多普勒激光光谱学是合适的工具,但在分析重双原子的精细和超精细结构时,它的局限性已经达到了。双共振技术有助于简化密集光谱和分配谱线。如果在单频激光之外使用微波辐射,则可以独立研究单个电子状态中的小能量分裂。最近开发的微波偏振光谱(MOPS)1已被证明可以提供研究低浓度化学不稳定物质所需的高分辨率和灵敏度。如果可以产生该物质的光束,则可以使用分子束激光-微波双共振技术以10 khz的精度测量外场中的基态能级分裂和移位这些方法的威力已经在碱土单卤化物自由基的应用中得到了证明。揭示了激发态的局部摄动,并通过超精细结构和斯塔克效应测量得到了电子结构的细节。
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