Ferricenium benzyltriethylammonium ?-oxobis[trichloroferrate(III)], the first isolated oxodiferrate of the double salt type

1986 ◽  
Vol 11 (2) ◽  
pp. 70-71 ◽  
Author(s):  
Eberhard W. Neuse ◽  
Fathima B. D. Kahn
Keyword(s):  
2021 ◽  
pp. 116452
Author(s):  
Tomasz Rzemieniecki ◽  
Marta Wojcieszak ◽  
Katarzyna Materna ◽  
Tadeusz Praczyk ◽  
Juliusz Pernak

1958 ◽  
Vol 36 (11) ◽  
pp. 1511-1517 ◽  
Author(s):  
A. N. Campbell ◽  
E. M. Kartzmark ◽  
E. G. Lovering

In the reciprocal salt pair Li2, K2, Cl2, SO4, and water, at 25 °C there are large areas in which potassium sulphate and potassium lithium sulphate (KLiSO4) are separately in equilibrium with solution. Two incongruent invariant points exist. At one of these the composition of the solution is 0.917 mole fraction chloride, 0.437 mole fraction lithium, and 19.4 moles of water per total mole of salt, the equilibrium solid phases being potassium chloride, potassium sulphate, and the double salt. At the second, the composition of the solution is 0.967 mole fraction chloride, 0.870 mole fraction lithium, and 13.8 moles of water per mole of salt, the solid phases being potassium chloride, double salt, and lithium sulphate monohydrate. One congruent invariant point exists, at which the composition of the solution is 1.00 mole fraction chloride, 0.960 mole fraction lithium, and 9.6 moles of water per mole of salt, the solid phases being lithium sulphate monohydrate, lithium chloride monohydrate, and potassium chloride.In the reciprocal salt pair Li2, Na2, Cl2, SO4, and water, at 25 °C there is an incongruent invariant point at which the composition of the solution is 0.873 mole fraction chloride, 0.668 mole fraction lithium, and 15.1 moles water per total mole of salt, the solid phases being sodium chloride, solid solution of sodium and lithium sulphates, and lithium sulphate monohydrate. A congruent invariant point exists, at which the composition of the solution is practically entirely lithium chloride, the solid phases present being lithium chloride monohydrate, lithium sulphate monohydrate, and sodium chloride.


1989 ◽  
Vol 34 (2) ◽  
pp. 99-111 ◽  
Author(s):  
K.R. Patil ◽  
M.N. Kim ◽  
M.A.R. Eisa ◽  
F.A. Holland

2003 ◽  
Vol 174 (1) ◽  
pp. 182-188 ◽  
Author(s):  
Kenji Waizumi ◽  
Takami Matsumoto ◽  
Toshiya Abe ◽  
Nobuhiro Fukushima ◽  
Hideki Masuda

ChemInform ◽  
2006 ◽  
Vol 37 (33) ◽  
Author(s):  
A. Hammerschmidt ◽  
M. Doech ◽  
S. Puetz ◽  
H. Eckert ◽  
B. Krebs
Keyword(s):  

2017 ◽  
Vol 170 ◽  
pp. 149-159 ◽  
Author(s):  
Andrea Gutierrez ◽  
Svetlana Ushak ◽  
Veronica Mamani ◽  
Pedro Vargas ◽  
Camila Barreneche ◽  
...  

IUCrData ◽  
2016 ◽  
Vol 1 (2) ◽  
Author(s):  
Ioannis Tiritiris ◽  
Thomas Schleid

In the crystal structure of the hydrated double salt, Cs+·[N(CH3)4]+·[B12H12]2−·H2O, the asymmetric unit contains one caesium and one tetramethylammonium cation, one dodecahydrido-closo-dodecaborate anion and one water molecule. The Cs+cation is coordinated tetrahedrally by four [B12H12]2−clusters, with the water molecule completing the coordination sphere. The tetramethylammonium cation is surrounded distorted octahedrally by six [B12H12]2−anions. The crystal structure is stabilized by a three-dimensional network of O—H...H—B and C—H...H—B dihydrogen bonds.


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