scholarly journals Crystal structure, magneto-structural correlation, thermal and electrical studies of an imidazolium halometallate molten salt: (trimim)[FeCl4]

RSC Advances ◽  
2020 ◽  
Vol 10 (19) ◽  
pp. 11200-11209 ◽  
Author(s):  
Palmerina González-Izquierdo ◽  
Oscar Fabelo ◽  
Garikoitz Beobide ◽  
Israel Cano ◽  
Idoia Ruiz de Larramendi ◽  
...  

We present a novel halometallate molten salt based on imidazolium cation with two structural transitions from 100 to 400 K which has been studied by X-ray and neutron diffraction techniques. Furthermore, the magnetic structure at low temperature and the ionic conductivity is also described.

RSC Advances ◽  
2020 ◽  
Vol 10 (28) ◽  
pp. 16826-16826
Author(s):  
Palmerina González-Izquierdo ◽  
Oscar Fabelo ◽  
Garikoitz Beobide ◽  
Israel Cano ◽  
Idoia Ruiz de Larramendi ◽  
...  

Correction for ‘Crystal structure, magneto-structural correlation, thermal and electrical studies of an imidazolium halometallate molten salt: (trimim)[FeCl4]’ by Palmerina González-Izquierdo et al., RSC Adv., 2020, 10, 11200–11209. DOI: 10.1039/D0RA00245C.


Author(s):  
H. J. Berthold ◽  
E. Vonholdt ◽  
R. Wartchow ◽  
T. Vogt

AbstractNHA single crystal structure analysis of NThe deuterated compound NThe structures of the ordered low temperature phases will be reported separately.


1997 ◽  
Vol 53 (1) ◽  
pp. 135-142 ◽  
Author(s):  
D. L. Corker ◽  
A. M. Glazer ◽  
J. Dec ◽  
K. Roleder ◽  
R. W. Whatmore

The crystal structure of the perovskite lead zirconate PbZrO3 has been redetermined using single-crystal X-ray diffraction (Mo Kα radiation, λ = 0.71069 Å). Single-crystal data at 100 K: space group. Pbam, a = 5.884 (1), b = 11.787 (3), c = 8.231 (2) Å, V = 570.85 Å3 with Z = 8, μ = 612.6 cm−1, D x = 8.06 Mg m−3, F(000) = 1168, final R = 0.033, wR = 0.061 over 555 reflections with I > 2σ(I). An investigation is made into previous contradicting reports of a possible disorder in the O atoms and their origin by examining the crystal pseudo-symmetry. Information distinguishing an ordered and disordered oxygen substructure is shown to reside in weak l odd reflections. Because of their extremely low intensities these reflections have not contributed sufficiently in previous X-ray structure investigations and hence, to date, conclusive evidence differentiating between ordered and disordered models has not been possible. By collecting single-crystal X-ray data at low temperature and by using exceptionally long scans on selected hkl, l odd, reflections, a new accurate structure determination is presented and discussed, showing the true ordered oxygen positions. Because of the large difference in scattering factors between lead and oxygen when using X-rays, a neutron diffraction Rietveld refinement using polycrystalline samples (D1A instrument, ILL, λ = 1.90788 Å) is also reported as further evidence to support the true ordered oxygen structure revealed by the low-temperature X-ray analysis.


1996 ◽  
Vol 49 (5) ◽  
pp. 633 ◽  
Author(s):  
BN Figgis ◽  
PA Reynolds ◽  
FK Larsen ◽  
GA Williams ◽  
CD Delfs

The crystal structure of [As(C6H5)4] [TcNCl4] was determined at 120 K by X-ray diffraction and at 28 K by neutron diffraction. The crystals are tetragonal, space group P4/n, with a 1260.4(3) and c 773.2(2) pm at 120 K. The [TcNCl4]-anion possesses exact C4v symmetry, with Tc≡N distances of 160.3(2) and 162.5(4)pm at 120 and 28 K respectively. Magnetic susceptibilities were measured on single crystals from 300 to 4.5 K. The results indicate a well behaved S ½ system following the Curie-Weiss law with θ -0.13 K


2013 ◽  
Vol 58 (4) ◽  
pp. 575-585 ◽  
Author(s):  
N. B. Bolotina ◽  
A. I. Kalyukanov ◽  
T. S. Chernaya ◽  
I. A. Verin ◽  
I. I. Buchinskaya ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document