Raman spectra of the double-anion salts M3ZnCl4NO3 (M+ = K+, Rb+, NH4+)

Authors
Citation
Rl. Carter, Raman spectra of the double-anion salts M3ZnCl4NO3 (M+ = K+, Rb+, NH4+), SPECT ACT A, 56(12), 2000, pp. 2351-2363
Citations number
49
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
ISSN journal
13861425 → ACNP
Volume
56
Issue
12
Year of publication
2000
Pages
2351 - 2363
Database
ISI
SICI code
1386-1425(20001101)56:12<2351:RSOTDS>2.0.ZU;2-Z
Abstract
Recently characterized K3ZnCl4NO3 and (NH4)(3)ZnCl4NO3, and newly prepared Rb3ZnCl4NO3 constitute a limited series of isomorphous double-anion salts ( space group Pnma, Z = 4). Room-temperature (295 K) Raman spectra from polyc rystalline samples of the compounds are reported and interpreted on the bas is of the C-s site symmetry of the ZnCl42- - and NO3- ions with reference t o the D-2h factor group of the unit cell. The spectra are compared with Ram an spectra of the corresponding M2ZnCl4 and MNO3 single-anion salts. Relati ve positions and frequencies of the ZnCl42- modes vary considerably among t he M3ZnCl4NO3 compounds, despite the isomorphism. The NO3- modes are more s imilar in all three compounds. The NO3- doubly degenerate v(3) and v(4) mod es are split into two distinct bands as a result of the decent in symmetry from D-3h for the free ion to C-s at the crystallographic site. The unequal intensities of the v(3), bands observed for K3ZnCl4NO3 and Rb3ZnCl4NO3 and the equal intensities of the v, bands observed for all three compounds sug gest the same factor-group assignments as the high-temperature phase NH,NO, (III). The free-ion Raman-inactive planar deformation mode, v,, is evident in all three compounds, but with lesser intensity than its overtone 2v(2). In K3ZnCl4NO3 and Rb3ZnCl4NO3, the symmetric stretching band, in addition t o the Very strong component for v,, shows a weak, low-frequency band found in many ionic nitrates, which has been attributed to thermally disordered n itrate ions or hot bands. This feature is not found in the spectrum of (NH4 )(3)ZnCl4NO3. The 12 NH4+ ions in the unit cell of (NH4)(3)ZnCl4NO3, which occupy C-1 and C-2 sites in a 2:1 ratio, give rise to extremely broad bands that show no evidence of the individual symmetry distinctions of the catio ns. The broad band from NH4+ v(4) obscures the region in which NO3- v(3) ba nds are expected, but the NO3- overtone 2v(2) is evident as a sharp peak ab ove a similarly broad band from NH4+ v(2). (C) 2000 Elsevier Science B.V. A ll rights reserved.