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Sub-collision hyperfine structure of nonlinear-optical resonance with field scanning

机译:场扫描非线性光学共振的亚碰撞超精细结构

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摘要

Some experimental evidences for methane are produced that the simple transition from frequency scanning of nonlinear-optical resonances to magnetic one may be accompanied with transition from sub-Doppler collisionally broadened structure to sub-collision hyperfine one. It is conditioned by nonlinearity of splitting of hyperfine sublevel for molecules in the adiabatically varied magnetic field and respectively breaking the analogy of magnetic and frequency scannings. The exact calculation of the resonance structure is considered for molecules with only one spin subsystem. The approximately spin-additive calculation of the structure is given for sufficiently fast rotating molecules with greater number of spin subsystems. Within the same approximation an example of hyperfine doubling in the magnetic and electric spectra of nonlinear-optical resonance is considered for fluoromethane.
机译:甲烷的一些实验证据表明,从非线性光学共振的频率扫描到磁性原子的简单转变可能伴随着从亚多普勒碰撞加宽结构到亚碰撞超精细结构的转变。它的条件是,绝热变化的磁场中分子的超精细子级分裂的非线性,并分别打破了磁扫描和频率扫描的类比。对于仅具有一个自旋子系统的分子,考虑了共振结构的精确计算。对于具有大量自旋子系统的足够快速旋转的分子,给出了该结构的近似自旋加法计算。在相同的近似值范围内,对于氟甲烷,考虑了在非线性光学共振的电磁谱和电谱中超精细加倍的示例。

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