ChemInform Abstract: STUDY OF THE DISSOLUTION OF ALUMINUM BROMIDE AND ALKALI METAL BROMIDES IN PROPYLENE CARBONATE. DISSOCIATION, RADIUS AND SOLVATION NUMBER OF IONS

1978 ◽  
Vol 9 (37) ◽  
Author(s):  
Y. MARY
1995 ◽  
Vol 60 (7) ◽  
pp. 1158-1161
Author(s):  
Jiří Vondrák

Electrochemical insertion of sodium or lithium into carbon black electrodes from perchlorate-propylene carbonate solution occurs under formation of substances close to C12Na and C6Li in potential range from 1.0 to 0 V vs alkali metal electrodes.


1975 ◽  
Vol 28 (2) ◽  
pp. 237 ◽  
Author(s):  
JW Diggle ◽  
AJ Parker ◽  
DA Owensby

The standard electron-transfer heterogeneous rate constant of lithium, potassium, sodium and caesium amalgams in N,N-dimethylformamide was ascertained employing cyclic voltammetry in an effort to relate the presence of a non-equilibrium electrode reaction at the dropping lithium amalgam electrode to the variation of the lithium amalgam electrode potential with amalgam electrode con- figuration, i.e. whether streaming, dropping or stationary. Such variations are not observed at other alkali metal amalgam electrodes. ��� In the dipolar aprotic solvents the standard electron-transfer heterogeneous rate constant for the Li(Hg) electrode increases as the solvating power for Li+ decreases, i.e. dimethyl sulphoxide < di- methylformamide < propylene carbonate. Water is a much stronger solvator of Li+ than is propylene carbonate, but the electron transfer is faster in water than in propylene carbonate; the important role of entropic contributions in ion solvation is discussed as an explanation.


ChemInform ◽  
2011 ◽  
Vol 43 (1) ◽  
pp. no-no
Author(s):  
Katsuhiko Moriyama ◽  
Yuta Izumisawa ◽  
Hideo Togo

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