Spectra of isomeric a-chloro fluorotoluenes in vapour state

1975 ◽  
Vol 72 ◽  
pp. 92-96 ◽  
Author(s):  
D. R. Singh ◽  
U. S. Tripathi ◽  
G. N. R. Tripathi
Keyword(s):  

Mercury molecules in the vapour state have never been directly detected. The ratio of the specific heats and vapour density determinations all show that mercury vapour is strictly monatomic, so that so far as chemical evidence is concerned mercury vapour molecules do not exist. However, the occurrence of quite strong hands in the absorption and emission spectra of mercury vapour at high pressure demand the presence of molecules in considerable number. We have obtained definite evidence that diatomic molecules are formed in mercury vapour by the attachment of excited atoms to normal atoms. The formation of the molecules in this way clearly reconciles the chemical evidence of their non-existence with Ike hand spectra evidence of their presence; for, unless the atoms are excited by light or electron impact, the vapour may remain practically monatomic.


1996 ◽  
Vol 57 (6-8) ◽  
pp. 1141-1144 ◽  
Author(s):  
M. Sebti ◽  
J. Ghanbaja ◽  
A. Merlin ◽  
D. Billaud
Keyword(s):  

1980 ◽  
Vol 33 (8) ◽  
pp. 1635 ◽  
Author(s):  
L Radom ◽  
NV Riggs

Formimide (diformamide), the parent of the diacylamines, is capable of existing in three basic ground-state conformations about the N-C bonds. Full geometry optimization with the STO-3G basis set predicts that all three conformers are fully coplanar, that the E,E (1) and E,Z(3) conformers are of similar energy, and that the Z,Z (2) conformer is of somewhat higher energy (by 11 kJ mol-1); 4-31G evaluation of the energies suggests that (2) is by far the least stable and that (1) is of higher energy than (3) by 6.5 kJ mol-1. Analysis of the calculated charge distribution suggests that (2) is destabilized by electrostatic repulsion. These results are consistent with experimental conclusions that planar (3) is strongly preferred in the vapour state at room temperature and that (2) has not been observed in the vapour state or in solution. Partial geometry optimization with the STO-3G basis set of model transition states for internal rotation suggests a barrier height of 52 kJ mol-1 (72 kJ mol-1 when evaluated with the 4-31G basis set) for the conversion (3) → (1).


Theories of the optical behaviour of liquids generally base themselves on the postulate that the well-known Lorentz formula ( n 2 — 1)/( n 2 + 2)ρ = constant correctly expresses the relation between the refractive index and density of a liquid. It has long been known, however, that this formula is at best only an approximation. The quantity ( n 2 — 1)/( n 2 + 2)ρ is found experimentally to be not invariable, its deviation from constancy becoming more and more marked as the density is increased. The change in the value of ( n 2 — 1)/( n 2 + 2)ρ in passing from the state of vapour to that of a liquid under ordinary conditions, is usually quite appreciable, as might be instanced by the case of benzene, for which Wasastjerna found for the D-line a molecular refraction of 27·20 in the vapour state, while the corresponding value for the liquid is 26·18, that is, 3·8 per cent, lower. The deviations from the Lorentz formula appear most striking when we use it to compute the change in the refractive index of a liquid produced by alterations of temperature or pressure. Here, again, we might instance the case of benzene, for which the observed value of dn / dt = —6·4 × 10 -4 per degree Centigrade for the D-line at 20° C., and that of dn / dp = —5·06 × 10 -5 per atmosphere, while the calculated values are dn / dt = —7·15 × 10 -4 and dn / dp = —5·66 × 10 -5 . The observed values are thus numerically about 10 per cent, smaller in either case, indicating that ( n 2 — 1)/( n 2 + 2)ρ diminishes more and more quickly as the density is increased. An expression of the form ( n 2 — 1)/( n 2 + 2)ρ = a — b ρ 2 where a and b are positive constants, has been found to represent the refraction of carbon dioxide over a wide range of density more closely than the original Lorentz formula. It has been deduced theoretically on certain suppositions regarding the magnitude of the polarisation field in liquids, which are, however, somewhat arbitrary in nature. Considering next the electrical behaviour of liquids, we find that the formula proposed by Debye (ε — l)/(ε + 2)ρ = A + B/T is not adequate to explain the dielectric properties of many known liquids. To illustrate this, we may again consider the case of benzene, whose dielectric constant has been determined over a wide range of temperatures and pressures. Since A and B in the formula are essentially positive constants, it follows that (ε — l)/(ε + 2)ρ should remain invariable when the liquid is compressed isothermally, and that it should diminish with rising temperature. Actually it is found with benzene that the quantity in question falls steadily with increasing pressure and increases with rising temperature. A similar apparently anomalous behaviour is shown by many other liquids whose molecules have a negligible electrical polarity. Liquids of marked electrical polarity show a diminution of (ε — l)/(ε + 2)ρ with rising temperature as demanded by the formula, but they deviate from it by showing a diminution of the same quantity when isothermally compressed, the latter effect being usually even more marked than for non-polar compounds.


Nature ◽  
1936 ◽  
Vol 137 (3464) ◽  
pp. 496-496 ◽  
Author(s):  
MD. ISRARUL HAQ ◽  
R. SAMUEL

In some previous papers it has been shown by the author and others that saturated compounds of most substances in the vapour state show continuous absorption. A typical example is SO 3 -vapour, which was recently studied by the author and which enabled him to make an accurate estimation of the heat of dissociation of oxygen. In the present work, the absorption spectrum of N 2 O was investigated with a view to determining the heat of dissociation of nitrogen. Leifson was the first to investigate the absorption spectrum of N 2 O gas and found that the gas shows no selective absorption in the Schumann region. He states that the absorption is in the form of two continuous bands, the first extending from λ 2000 to λ 1680 and the second from λ 1550 beyond the range of observation. Recently Wulf and Melvin showed that when N 2 O is illuminated with light of wave-length λ 2300, it is decomposed photochemically into NO and N; they also noticed that N 2 O possesses no band absorption.


Sign in / Sign up

Export Citation Format

Share Document