Systems xenon hexafluoride-germanium tetrafluoride and xenon hexafluoride-silicon tetrafluoride

1967 ◽  
Vol 6 (7) ◽  
pp. 1300-1302 ◽  
Author(s):  
Kent E. Pullen ◽  
George H. Cady
1973 ◽  
Vol 3 (1) ◽  
pp. 117-118 ◽  
Author(s):  
Djordje R. Stojaković ◽  
Slobodan D. Radosavljević ◽  
Vera Č. Šćepanović

1970 ◽  
Vol 24 ◽  
pp. 864-870 ◽  
Author(s):  
D. Bratland ◽  
A. Fekri ◽  
K. Grjotheim ◽  
K. Motzfeldt ◽  
S. E. Rasmussen ◽  
...  

1968 ◽  
Vol 46 (6) ◽  
pp. 987-993 ◽  
Author(s):  
J. P. Guertin ◽  
M. Onyszchuk

Tensimetric titrations at −78° of silicon tetrafluoride with ethylene oxide, trimethylene oxide, tetrahydrofuran, tetrahydropyran, and dimethyl ether prove the formation of only 1:2 complexes, SiF4•2-(ether). All are unstable at 25° and either dissociate completely, as do SiF4•2(CH2)4O, SiF4•2(CH2)5O, and SiF4•2(CH3)2O, or decompose into SiF4 and a polymethylene oxide polymer, as do SiF4•2(CH2)2O and SiF4•2(CH2)3O. Silicon tetrafluoride does not coordinate with 1,4-dioxane in the range −94 to 25° and less than 1 atm pressure. Condensed phase heats of dissociation of SiF4•2(ether) complexes follow the order (CH2)3O > (CH2)4O > (CH2)5O ≥ (CH2)2O > (CH3)2O, which suggests that this is the relative order of basicities towards SiF4.


Nature ◽  
1951 ◽  
Vol 168 (4274) ◽  
pp. 557-557 ◽  
Author(s):  
A. D. CAUNT ◽  
L. N. SHORT ◽  
L. A. WOODWARD

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