z-logo
open-access-imgOpen Access
Structure, Phonon Properties, and Order–Disorder Transition in the Metal Formate Framework of [NH4][Mg(HCOO)3]
Author(s) -
Mirosław Mączka,
A. Pietraszko,
B. Macalik,
K. Hermanowicz
Publication year - 2014
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/ic4020702
Subject(s) - chemistry , raman spectroscopy , phase transition , crystallography , ion , formate , crystal structure , diffraction , crystal (programming language) , dielectric , phase (matter) , phonon , x ray crystallography , transition metal , condensed matter physics , optics , materials science , organic chemistry , catalysis , physics , biochemistry , programming language , optoelectronics , computer science
We report the synthesis, crystal structure, thermal, dielectric, IR, and Raman studies of [NH4][Mg(HCOO)3] formate. Single-crystal X-ray diffraction shows that it crystallizes in the hexagonal space group P6322, with orientationally disordered NH4(+) ions located in the cages of the network. Upon cooling, [NH4][Mg(HCOO)3] undergoes a phase transition at around 255 K to the ferroelectric P63 structure. Raman and IR spectra show a strong increase in intensity of the N-H stretching bands as well as narrowing of the bands related to the NH4(+) ions upon cooling. These changes indicate that the phase transition is due to orientational ordering of the NH4(+) ions. Analysis of the Raman data show, however, that the rotational and translational motions of NH4(+) do not freeze completely at the phase transition but exhibit further slowing down below 255 K, and the motional freezing becomes nearly complete below 140 K.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom