scholarly journals Using quadrature and an iterative eigensolver to compute fine-structure ro-vibrational levels of Van der Waals complexes: NH(Σ−3)–He, O2(Σg−3)–Ar, and O2(Σg−3)–He

2019 ◽  
Vol 151 (5) ◽  
pp. 054101 ◽  
Author(s):  
Xiao-Gang Wang ◽  
Tucker Carrington
Keyword(s):  
Fine Structure ◽  
Van Der Waals ◽  
Van Der Waals Complexes ◽  
Vibrational Levels

Spectra of (H2)2, (D2)2, and H2–D2 Van der Waals Complexes

1974 ◽  
Vol 52 (12) ◽  
pp. 1082-1089 ◽  
Author(s):  
A. R. W. McKellar ◽  
H. L. Welsh
Keyword(s):  
Fine Structure ◽  
Nuclear Spin ◽  
Selection Rule ◽  
Van Der Waals ◽  
Rotational Quantum Number ◽  
Van Der Waals Complexes ◽  
Not Given ◽  
Simple Effect ◽  
Anisotropic Force ◽  
Nuclear Spin Statistics

Spectra due to the Van der Waals complex (H2)2 have been obtained with greatly improved resolution, and analogous spectra of (D2)2 and H2–D2 have been observed. The experiments were conducted with an absorption path of 110 m in a multiple traversal cell at temperatures between 16 and 21 K. The spectra are manifested as fine structure accompanying the single and double H2 (or D2) transitions in the hydrogen (or deuterium) collision induced fundamental band. The observed structure for (H2)2 and H2–D2 can be unambiguously assigned to rotational transitions of the complex governed by the selection rule Δl = ± 1, ± 3, where l is the rotational quantum number of the complex. A detailed analysis must include anisotropic force effects, and is not given here. The spectrum of (D2)2 is complicated, not only by anisotropic force effects, but also by mutual perturbations between the rotational levels of the upper states of corresponding single and double D2 transitions; for this reason, the assignments suggested are somewhat uncertain. An interesting intensity alternation apparent in part of the (D2)2 spectrum is explained as a simple effect of nuclear spin statistics in the pseudodiatomic molecule (D2)2.

scholarly journals How accurate is the determination of equilibrium structures for van der Waals complexes? The dimer N2O⋯CO as an example

2021 ◽  
Vol 154 (19) ◽  
pp. 194302
Author(s):  
Jean Demaison ◽  
Natalja Vogt ◽  
Yan Jin ◽  
Rizalina Tama Saragi ◽  
Marcos Juanes ◽  
...  
Keyword(s):  
Van Der Waals ◽  
Van Der Waals Complexes ◽  
Equilibrium Structures

scholarly journals Consecutive Vibrational Redistribution and Predissociation Processes in s-Tetrazine–Argon Van Der Waals Complexes

1983 ◽  
Vol 2 (3-4) ◽  
pp. 125-135 ◽  
Author(s):  
J. J. F. Ramaekers ◽  
L. B. Krijnen ◽  
H. J. Lips ◽  
J. Langelaar ◽  
R. P. H. Rettschnick
Keyword(s):  
Decay Time ◽  
Van Der Waals ◽  
Stagnation Pressure ◽  
Van Der Waals Complexes ◽  
Supersonic Expansion ◽  
Vibrational Predissociation ◽  
Out Of Plane ◽  
Spectrally Resolved ◽  
Plane Mode

s-Tetrazine argon complexes T−Arn (n = 1, 2) are formed in a supersonic expansion of argon seeded with s-tetrazine. The expansion was conducted through a nozzle of 50 or 100 μm with an argon stagnation pressure between 1 and 1.5 bar. From spectrally resolved measurements it is clear that vibrational redistribution processes as well as vibrational predissociation processes take place after SVL excitation within the complex.From rise and decay time experiments it can be concluded, that after excitation of the 6a1 complex level, the above mentioned processes are consecutive and not parallel. It appears that the out of plane mode 16a couples with the Van der Waals stretching mode. The predissociation rate of the 16a2 complex is observed to be 2.3 × 109 s−1.

Van der Waals Complexes of Cu, Ag, and Au with Hydrogen Sulfide. The Bonding Character

2007 ◽  
Vol 111 (50) ◽  
pp. 13238-13244 ◽  
Author(s):  
Jaroslav Granatier ◽  
Miroslav Urban ◽  
Andrzej J. Sadlej
Keyword(s):  
Hydrogen Sulfide ◽  
Van Der Waals ◽  
Van Der Waals Complexes
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