Influence of Pseudo-Alkali Cations on Network Depolymerization in Mixed-Cation Germanate Glasses

1973 ◽  
Vol 56 (1) ◽  
pp. 25-30 ◽  
Author(s):  
E. F. RIEBLING
2021 ◽  
Vol 13 (36) ◽  
pp. 43573-43586
Author(s):  
Suresh Maniyarasu ◽  
J. Chun-Ren Ke ◽  
Ben F. Spencer ◽  
Alex S. Walton ◽  
Andrew G. Thomas ◽  
...  

2014 ◽  
Vol 70 (11) ◽  
pp. 1036-1039 ◽  
Author(s):  
Stefanie Gärtner ◽  
Christof Suchentrunk ◽  
Nikolaus Korber

The involvement of two different alkali cations in the nonagermanide ammoniate Cs3.2Na0.8Ge9·5.3NH3[tricaesium sodium nonagermanide–ammonia (1/5.3)] provides insights into the coordination behaviour of ammonia towards sodium and caesium cations within one compound and represents the first mixed-cationic solvate structure of nonagermanide tetraanions. The compound crystallizes in the monoclinic space groupP21/mand, with the presence of pseudomerohedral twinning, mixed-cation sites and disordering of the nonagermanide cage anions, features a combination of crystallographic challenges which could all be resolved during the refinement.


2018 ◽  
Vol 11 (10) ◽  
pp. 2876-2883 ◽  
Author(s):  
Maria R. Lukatskaya ◽  
Jeremy I. Feldblyum ◽  
David G. Mackanic ◽  
Franziska Lissel ◽  
Dominik L. Michels ◽  
...  

Challenge of developing new formulations of water-in-salt electrolytes are addressedviamixed cation strategy: cheaper (by at least an order of magnitude) and more soluble salts featuring alkali cations beyond lithium, such as potassium, are used to create the water-in-salt condition.


1980 ◽  
Vol 45 (2) ◽  
pp. 369-375 ◽  
Author(s):  
Stanislav Miertuš ◽  
Ondrej Kyseľ

The 4-nitrobenzophenone radical anion prepared by electrolysis was studied by ESR spectroscopy. On the basis of the interpretation of ESR spectra, the conformation of this system was estimated. The effect of the concentration of supporting electrolyte and of the presence of a proton-donor agent (C2H5OH) was examined. It is assumed that changes in hyperfine splitting constants are caused by association.


2019 ◽  
Vol 74 (4) ◽  
pp. 357-363
Author(s):  
Daniela Vitzthum ◽  
Hubert Huppertz

AbstractThe mixed cation triel borate Ga4In4B15O33(OH)3 was synthesized in a Walker-type multianvil apparatus at high-pressure/high-temperature conditions of 12.5 GPa and 1300°C. Although the product could not be reproduced in further experiments, its crystal structure could be reliably determined via single-crystal X-ray diffraction data. Ga4In4B15O33(OH)3 crystallizes in the tetragonal space group I41/a (origin choice 2) with the lattice parameters a = 11.382(2), c = 15.244(2) Å, and V = 1974.9(4) Å3. The structure of the quaternary triel borate consists of a complex network of BO4 tetrahedra, edge-sharing InO6 octahedra in dinuclear units, and very dense edge-sharing GaO6 octahedra in tetranuclear units.


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