Abstract

Theory of rotational distortion in multiplet band spectra.---Hund's theoretical interpretation of the contracting multiplet type band spectra for diatomic molecules is thrown into quantitative form for the doublet case and also for the extreme components of higher multiplicities. The discussion is based on the conventional Bohr theory.The ultra-violet OH bands.---The theory is applied to the ultra-violet doublet OH bands and is shown to be in approximate agreement with the data. Following suggestions of Mulliken these bands are interpreted as of the $^{2}S\ensuremath{\rightarrow}^{2}P$ type with the $^{2}P$ doublet inverted.

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