Hydrogen bonding in the gas phase: the thermodynamic properties of hydrogen fluoride-ether complexes and their far infrared spectra

The equilibrium constants of gas-phase complexes of HF with dimethyl, methyl ethyl and diethyl ether have been measured at several temperatures using the Benesi-Hildebrand approximation on the absorption band of the HF stretching vibration in the complex. From these, values of Δ H of — 43, — 38 and — 30 kJ mol -1 respectively, have been determined. They are interpreted in terms of conformational rearrangements of the ethers when they form hydrogen bonds. The far infrared spectra of the complexes with both HF and DF have also been recorded and in each case a band observed at around 180 cm -1 which is assigned to the intermolecular stretching mode of vibration. For the complex between HF and dimethyl ether a rotational contour has been observed at about 10 cm -1 .

Far infrared spectra of charge-transfer complexes between iodine and substituted pyridines, dissolved in cyclohexane, have been measured in the region 20 to 200 cm -1 . Bands have been assigned to the modified iodine molecule stretching vibration near 180 cm -1 , and to the stretching of the intermolecular bond in the range 65 to 95 cm -1 . The shifts of the vibration frequencies, and force constants calculated using a simple valency force field, have been discussed in relation to the mass, electronic and steric effects of substituent groups. Equilibrium constants for the formation of the complex have been determined. From the intensities of the absorption bands, further evidence has been found for a vibronic interaction, leading to a delocalization of the transition moment in the vibrations of the complexes, and to an enhancement of the intensity of absorption.


2020 ◽  
Vol 22 (14) ◽  
pp. 7497-7506 ◽  
Author(s):  
O. Palumbo ◽  
A. Cimini ◽  
F. Trequattrini ◽  
J.-B. Brubach ◽  
P. Roy ◽  
...  

DFT calculations with the ωB97-D functional reproduce hydrogen bonding features of the far-infrared spectra of diethylmethylammonium methanesulfonate and diethylmethylammonium trifluoromethanesulfonate.


1973 ◽  
Vol 51 (4) ◽  
pp. 514-519 ◽  
Author(s):  
A. B. P. Lever ◽  
B. S. Ramaswamy

The far infrared spectra of 16 adducts of pyridine, quinoline, isoquinoline, urea, aniline, o- and p-toluidine with copper acetate, propionate, and butyrate, and of copper formate tetrahydrate were recorded at ambient temperature and at −196 °C. A range of derivatives were prepared containing isotopically pure 65Cu. The spectra of these derivatives were used to identify, unequivocally, the copper–oxygen stretching frequencies.Complexes believed to be polymeric (aniline and toluidine adducts) exhibit one copper–oxygen stretching vibration between 300 and 350 cm−1 A second band, lying between 350 and 400 cm−1 is not isotopically sensitive. The dimeric complexes exhibit one or two bands in the 300–400 cm−1 region, all of which are isotopically sensitive. Certain of the amine adducts exhibit an isotopically sensitive band near 240 cm−1 assignable to a Cu—N stretching mode.


2015 ◽  
Vol 17 (21) ◽  
pp. 13790-13793 ◽  
Author(s):  
Ralf Ludwig

Challenging conventional wisdom: dispersion forces can compete with hydrogen bonding in ionic liquids.


1985 ◽  
Vol 40 (10) ◽  
pp. 989-994 ◽  
Author(s):  
Hans Bürger ◽  
Martina Betzel

Fourier Transform far infrared spectra of unstable stannyl chloride, bromide and iodide have been measured in the gas phase with a resolution of 0.04 cm-1. At pressures below 10 mbar, their lifetimes at 0 °C in preconditioned cells were found to be 10-30 min. The v3 fundamentals and hot bands of the series (n + 1)v3 - nv3 have been observed. Rotational J structure has been resolved for monoisotopic samples, and band origins v30, anharmonicity constants x33, ɑ3B and DJ0 values have been determined from the rovibrational analyses. The following v30 values were obtained: H3116Sn35Cl 375.470 (5), H3116Sn37Cl 367.689 (6), H3116Sn79Br 263.566 (5) and H3116SnI 209.759 (6) cm-1.


1985 ◽  
Vol 63 (12) ◽  
pp. 1559-1562 ◽  
Author(s):  
M. J. Clouter ◽  
A. R. W. McKellar

Far-infrared (15–200 cm−1) absorption spectra of CO2 have been obtained (i) in the super-critical gas at 306 K with densities from 80 to 122 amagat, (ii) in the saturated liquid at 298, 272, and 236 K, and (iii) on the critical isochore in the temperature range 0.02 K < (T – Tc) < 2.0 K. The gas-phase measurements are in agreement with previous work, but an error in previously reported liquid-phase results is revealed. In contrast to the previous measurements of Mannik and Stryland on the ν1 band, the far-infrared spectra showed no measurable effects associated with density fluctuations in the critical region. A simple statistical theory is proposed to account for this result.


1983 ◽  
Vol 61 (7) ◽  
pp. 1449-1452 ◽  
Author(s):  
Marek J. Wójcik ◽  
Czesława Paluszkiewicz

Infrared spectra of hydrogen-bonded methyl salicylate have been studied in the temperature range 173–293 K, in solutions of various concentrations (in CCl4) and in the gaseous state. Results show that the molecules form monomerie intramolecular hydrogen bonds in the solid, liquid, and gaseous state. Far-infrared spectra were recorded which give the wavenumber of low-frequency O … O mode used in theoretical reconstruction of the band connected with the O—H stretching vibration. The position and especially the width of this band are determined to a large extent by the influence of the environment.


1974 ◽  
Vol 52 (7) ◽  
pp. 1081-1085 ◽  
Author(s):  
Hsiao-Chian Leung ◽  
Anthony Anderson

Infrared spectra, in the range 20–400 cm−1, of thin polycrystalline films (at 80 °K) of iodine monobromide and the β-form of iodine monochloride have been recorded. For IBr, the intramolecular stretching region shows two peaks separated by 16 cm−1 and shifted appreciably from the gas phase value, indicating strong intermolecular interactions. Four lattice modes are also observed and assigned in accordance with group theoretical predictions. For β-ICl the spectrum of the stretching region confirms the presence of two distinct molecules with different bond lengths. The complexity of the ICl structure prevents an assignment of the ten observed lattice absorptions.


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