Collisional Depolarization of Luminescence of Polyatomic Molecules with Internal Rotations

Author(s):  
A. P. Blokhin

The velocity of ultrasonic waves has been measured in a series of organic vapours at frequencies 566, 1192 and 4000 kc./sec., temperatures 20 and 100° C, and pressures ranging from 0.25 to 4 atm. Ultrasonic dispersion was found with benzene, cyclopropane and ethane. No dispersion was found with propane, n -hexane, cyclohexane, cyclohexene, ethylchloride, chloroform, acetonitrile, acetaldehyde, acetone, diethyl ether and methyl alcohol. The mechanism and rate of the activation of vibrational energy by intermolecular collisions are discussed in relation to molecular structure. It is concluded that, for polyatomic molecules in general, there is little hindrance to the interconversion of translational and vibrational energy, especially at high temperatures. Slow interconversion, leading to ultrasonic dispersion, only occurs with small or rigid molecules, where internal rotations or vibrations of low frequency are absent. Interchange of vibrational energy between the different modes within the molecule is usually very rapid.


2000 ◽  
Vol 98 (21) ◽  
pp. 1763-1770 ◽  
Author(s):  
Vincenzo Aquilanti, Andrea Beddoni, Simonett

1981 ◽  
Vol 134 (5) ◽  
pp. 45 ◽  
Author(s):  
V.S. Letokhov ◽  
A.A. Makarov
Keyword(s):  

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3484
Author(s):  
Felix Duensing ◽  
Elisabeth Gruber ◽  
Paul Martini ◽  
Marcelo Goulart ◽  
Michael Gatchell ◽  
...  

Complexes of atomic gold with a variety of ligands have been formed by passing helium nanodroplets (HNDs) through two pickup cells containing gold vapor and the vapor of another dopant, namely a rare gas, a diatomic molecule (H2, N2, O2, I2, P2), or various polyatomic molecules (H2O, CO2, SF6, C6H6, adamantane, imidazole, dicyclopentadiene, and fullerene). The doped HNDs were irradiated by electrons; ensuing cations were identified in a high-resolution mass spectrometer. Anions were detected for benzene, dicyclopentadiene, and fullerene. For most ligands L, the abundance distribution of AuLn+ versus size n displays a remarkable enhancement at n = 2. The propensity towards bis-ligand formation is attributed to the formation of covalent bonds in Au+L2 which adopt a dumbbell structure, L-Au+-L, as previously found for L = Xe and C60. Another interesting observation is the effect of gold on the degree of ionization-induced intramolecular fragmentation. For most systems gold enhances the fragmentation, i.e., intramolecular fragmentation in AuLn+ is larger than in pure Ln+. Hydrogen, on the other hand, behaves differently, as intramolecular fragmentation in Au(H2)n+ is weaker than in pure (H2)n+ by an order of magnitude.


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.


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