Room temperature spectroscopic investigations of (KNO3)-N-14, (KNO3)-N-15,(KNO3-x)-N-14-O-16 O-18(x) and a 1 : 1 mixture of (KNO3)-N-14 and (KNO3)-N-15: Intermolecular coupling revealed in the vibrational spectra

Citation
T. Chakraborty et al., Room temperature spectroscopic investigations of (KNO3)-N-14, (KNO3)-N-15,(KNO3-x)-N-14-O-16 O-18(x) and a 1 : 1 mixture of (KNO3)-N-14 and (KNO3)-N-15: Intermolecular coupling revealed in the vibrational spectra, J RAMAN SP, 30(3), 1999, pp. 189-194
Citations number
20
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
JOURNAL OF RAMAN SPECTROSCOPY
ISSN journal
03770486 → ACNP
Volume
30
Issue
3
Year of publication
1999
Pages
189 - 194
Database
ISI
SICI code
0377-0486(199903)30:3<189:RTSIO(>2.0.ZU;2-S
Abstract
The diffuse reflectance Fourier transform IR (DRIFT) and Raman spectra for microcrystalline (KNO3)-N-14, (KNO3)-N-15, (KNO3-xOx)-N-14-O-16-O-18 and a 1:1 mixture of (KNO3)-N-14 and (KNO3)-N-15 were measured at room temperatur e. A new assignment for the observed factor group split components of the a symmetric N-O stretching mode and infrared evidence for the existence of dy namically disordered NO3- ions is proposed. Attractive intermolecular dipol ar interaction among the NO3- ions along the chain is invoked to explain th e spectral features around the asymmetric stretching mode region in the Ram an spectrum of the 1:1 mixed salt of (KNO3)-N-14 and (KNO3)-N-15. Analysis of the experimental data for the oxygen-enriched salt also demonstrates the existence of intermolecular coupling in the asymmetric stretching mode reg ion. The intensities of the Raman components of the totally symmetric N-O s tretching and in-plane bending mode regions correlate almost quantitatively with the calculated distribution of the various isotopes of NO3- ions in O -18-enriched KNO3. The IR intensity of the corresponding bands, on the othe r hand, is dependent on the symmetry of the respective isotopic species. Co pyright (C) 1999 John Wiley & Sons, Ltd.