scholarly journals On the absorption of light by gaseous, liquid and solid xenon

The result of studies made by McLennan and McLeod and by McLennan, Smith and Wilhelm on the Raman effects obtained with liquid hydrogen have made it abundantly clear that molecules of hydrogen in the liquid phase exist or can exist in electronic, vibrational and rotational states that are exactly the same as states that are available for them to assume in the form of a gas or as isolated units. The same is true in regard to energy states that molecules of oxygen or of nitrogen may take up when existing as isolated entities on the one hand or when existing as a gas or a liquid on the other. In so far as oxygen is concerned, it is known from the work of Babcock that practically all the molecules of oxygen in the earth’s atmosphere are in the electronic state of lowest energy possible for them to assume. Only a very small percentage of them, namely, 0·04 per cent., have even one quantum of vibrational energy. It has been shown by McLennan, Smith and Wilhelm that a similar statement applies in a description of the energy states of the molecules of oxygen as they exist in the liquid or in the solid phase. The band systems and the structures of the band system that characterise the absorption spectra of gaseous, liquid and solid oxygen are identical. These bands all originate in transitions to higher energy states from rotational vibrational energy levels associated with a fundamental 3 Ʃ electronic energy state that can be shown by the theory of Hund and Mullikan to be the most stable one that molecules of oxygen can assume.

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Liu Sun ◽  
Li Zhao ◽  
Rui-Yun Peng

AbstractWith the rapid development of terahertz technologies, basic research and applications of terahertz waves in biomedicine have attracted increasing attention. The rotation and vibrational energy levels of biomacromolecules fall in the energy range of terahertz waves; thus, terahertz waves might interact with biomacromolecules. Therefore, terahertz waves have been widely applied to explore features of the terahertz spectrum of biomacromolecules. However, the effects of terahertz waves on biomacromolecules are largely unexplored. Although some progress has been reported, there are still numerous technical barriers to clarifying the relation between terahertz waves and biomacromolecules and to realizing the accurate regulation of biological macromolecules by terahertz waves. Therefore, further investigations should be conducted in the future. In this paper, we reviewed terahertz waves and their biomedical research advantages, applications of terahertz waves on biomacromolecules and the effects of terahertz waves on biomacromolecules. These findings will provide novel ideas and methods for the research and application of terahertz waves in the biomedical field.


2007 ◽  
Vol 245 (2) ◽  
pp. 115-125 ◽  
Author(s):  
Tibor Furtenbacher ◽  
Attila G. Császár ◽  
Jonathan Tennyson

RSC Advances ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 3613-3621
Author(s):  
Yonghong Xu ◽  
Huihui Wang ◽  
Yonggang Yang ◽  
Changyong Li ◽  
Liantuan Xiao ◽  
...  

The band structures of the vibrational energy levels of B11− lead to corresponding spectral broadening. The vibrational band-structures of planar boron rotors are caused by internal rotations.


2019 ◽  
Vol 118 (2) ◽  
pp. e1597199
Author(s):  
Lulu Zhang ◽  
Daguang Yue ◽  
Juan Zhao ◽  
Yuzhi Song ◽  
Qingtian Meng

Author(s):  
Karl Irikura

When computing the potential-energy curve of a diatomic molecule for predictive spectroscopy, high-level calculations are usually desired. The best calculations are expensive, so few points are usually available. The points are fitted to a continuous function, such as a polynomial. Ro-vibrational energy levels are then computed using the fitted function, and spectroscopic constants extracted. However, there may be problems with overfitting, with inadequate flexibility of the fitting function, or with dependence of results upon the choice of fitting function. More fundamentally, the fitting function is selected using aesthetics or convenience, instead of physics. Here we suggest using a lower-level, high-resolution ab initio potential as a guide. Instead of fitting the sparse, high-level data directly, the energy differences between the high-level points and the guiding potential are fitted. The results are improved even with an inexpensive guiding potential. This simple strategy involves little additional effort and can be recommended for routine use. It is similar to some interpolation strategies in the literature of polyatomic molecules. When the guiding potential extends beyond the high-level data, extrapolations are also improved.


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