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Intermolecular H-bond in propan-2-ol and its solutions with acetonitrile
Formation of propan‐2‐ol–acetonitrile dimers is manifested in the Raman spectra as an appearance of a band of aggregates in the high‐wavenumber side of the CN vibrational band of liquid acetonitrile (∼2 cm−1). The intensity of the band of aggregates changes with a change in the concentration of the...
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Published in: | Journal of Raman spectroscopy 2007-12, Vol.38 (12), p.1633-1638 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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Online Access: | Get full text |
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Summary: | Formation of propan‐2‐ol–acetonitrile dimers is manifested in the Raman spectra as an appearance of a band of aggregates in the high‐wavenumber side of the CN vibrational band of liquid acetonitrile (∼2 cm−1). The intensity of the band of aggregates changes with a change in the concentration of the mixture (1–0.05 mole fraction).
For propan‐2‐ol we carried out nonempirical calculations of a structure of isolated dimer aggregates. The formation of an intramolecular H‐bond between the H and the O atom of the
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group of length 2.045 Å is possible in the monomer molecule. The CH3 groups of alcohol are not equivalent. In the dimer formation, intramolecular H‐bond in the \newbox\osprulebox
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$\osprule{{\rm HCO}}{2.5} \hbox{H}$
group is preserved. An intermolecular H‐bond of length 2.045 Å and energy 15 kJ/mole is formed between the H atom of one molecule and the O atom of another molecule of the OH. The length and energy of the H‐bond for the propan‐2‐ol–acetonitrile dimer formations calculate to 2.27 Å and 12.9 kJ/mole, respectively. The H‐bond is formed by σ‐electrons of nitrogen. The experimental data and the results of calculations are in good agreement. Copyright © 2007 John Wiley & Sons, Ltd. |
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ISSN: | 0377-0486 1097-4555 |
DOI: | 10.1002/jrs.1882 |