ChemInform Abstract: The Versatility of Solid-State Metathesis Reactions: From Rare Earth Fluorides to Carbodiimides.

ChemInform ◽  
2009 ◽  
Vol 40 (20) ◽  
Author(s):  
Leonid Unverfehrt ◽  
Jochen Glaser ◽  
Markus Stroebele ◽  
Sonja Tragl ◽  
Katharina Gibson ◽  
...  
2009 ◽  
Vol 635 (3) ◽  
pp. 479-483 ◽  
Author(s):  
Leonid Unverfehrt ◽  
Jochen Glaser ◽  
Markus Ströbele ◽  
Sonja Tragl ◽  
Katharina Gibson ◽  
...  

2021 ◽  
Vol 168 (3) ◽  
pp. 036502
Author(s):  
Andre Bents ◽  
Josef Maximilian Gerdes ◽  
Michael Ryan Hansen ◽  
Thomas Jüstel ◽  
Florian Baur

Author(s):  
N. M. P. Low ◽  
L. E. Brosselard

There has been considerable interest over the past several years in materials capable of converting infrared radiation to visible light by means of sequential excitation in two or more steps. Several rare-earth trifluorides (LaF3, YF3, GdF3, and LuF3) containing a small amount of other trivalent rare-earth ions (Yb3+ and Er3+, or Ho3+, or Tm3+) have been found to exhibit such phenomenon. The methods of preparation of these rare-earth fluorides in the crystalline solid form generally involve a co-precipitation process and a subsequent solid state reaction at elevated temperatures. This investigation was undertaken to examine the morphological features of both the precipitated and the thermally treated fluoride powders by both transmission and scanning electron microscopy.Rare-earth oxides of stoichiometric composition were dissolved in nitric acid and the mixed rare-earth fluoride was then coprecipitated out as fine granules by the addition of excess hydrofluoric acid. The precipitated rare-earth fluorides were washed with water, separated from the aqueous solution, and oven-dried.


2021 ◽  
Vol 122 ◽  
pp. 55-63
Author(s):  
S. Pavón ◽  
T. Lorenz ◽  
A. Fortuny ◽  
A.M. Sastre ◽  
M. Bertau

2020 ◽  
Vol 2020 (41) ◽  
pp. 3954-3958
Author(s):  
Danuta Dutczak ◽  
Amira Siai ◽  
Markus Ströbele ◽  
David Enseling ◽  
Thomas Jüstel ◽  
...  

2013 ◽  
Vol 68 (11) ◽  
pp. 1198-1206 ◽  
Author(s):  
Ernst Hinteregger ◽  
Michael Enders ◽  
Almut Pitscheider ◽  
Klaus Wurst ◽  
Gunter Heymann ◽  
...  

The new rare-earth fluoride borates RE2(BO3)F3 (RE=Tb, Dy, Ho) were synthesized under highpressure/ high-temperature conditions of 1:5 GPa=1200 °C for Tb2(BO3)F3 and 3:0 GPa=900 °C for Dy2(BO3)F3 and Ho2(BO3)F3 in a Walker-type multianvil apparatus from the corresponding rareearth sesquioxides, rare-earth fluorides, and boron oxide. The single-crystal structure determinations revealed that the new compounds are isotypic to the known rare-earth fluoride borate Gd2(BO3)F3. The new rare-earth fluoride borates crystallize in the monoclinic space group P21/c (Z = 8) with the lattice parameters a=16:296(3), b=6:197(2), c=8:338(2) Å , b =93:58(3)° for Tb2(BO3)F3, a= 16:225(3), b = 6:160(2), c = 8:307(2) Å , b = 93:64(3)° for Dy2(BO3)F3, and a = 16:189(3), b = 6:124(2), c = 8:282(2) Å , β= 93:69(3)° for Ho2(BO3)F3. The four crystallographically different rare-earth cations (CN=9) are surrounded by oxygen and fluoride anions. All boron atoms form isolated trigonal-planar [BO3]3- groups. The six crystallographically different fluoride anions are in a nearly planar coordination by three rare-earth cations.


Sign in / Sign up

Export Citation Format

Share Document