Hydrogen-bonded and ion-pair complexes in aprotic solvents

1975 ◽  
Vol 10 ◽  
pp. 29 ◽  
Author(s):  
J. E. Crooks ◽  
B. H. Robinson
1980 ◽  
Vol 33 (3) ◽  
pp. 491 ◽  
Author(s):  
B Poh ◽  
H Siow

Infrared and nuclear magnetic resonance spectroscopic methods were used to study the tropolonetriethylamine equilibria. In aprotic solvents tropolone transfers its proton to triethylamine to form an ion pair which is in equilibrium with the intramolecularly hydrogen-bonded tropolone. The extent of ion pair formation increases with the dielectric constant of the aprotic solvent. Unlike the case of the p- nitrophenol-triethylamine system, there is no formation of a hydrogen bonded complex between tropolone and triethylamine. In the case of the tropolone-dibutylamine system in aprotic solvents, only ion pair formation is observed.


1966 ◽  
Vol 19 (1) ◽  
pp. 43 ◽  
Author(s):  
WA Millen ◽  
DW Watts

Ion association constants at 30� have been determined for the cis-[Co en, Cl2]+Cl- ion pair in NN-dimethylformamide (DMF), NN-dimethylacetamide (DMA), and at 20.0�, 25.0�, and 30.0� in dimethyl sulphoxide (DMSO), by a spectrophotometric method. Association constants for the cis-[Co en2 Cl2]+Br- and the trans- [Co en2 Cl2]+Cl- ion pairs have also been determined in DMF at 30�.


1972 ◽  
Vol 76 (14) ◽  
pp. 1989-1993 ◽  
Author(s):  
R. A. Hudson ◽  
R. M. Scott ◽  
S. N. Vinogradov

1992 ◽  
Vol 11 (7) ◽  
pp. 2339-2341 ◽  
Author(s):  
Lee Brammer ◽  
Melinda C. McCann ◽  
R. Morris Bullock ◽  
Richard K. McMullan ◽  
Paul Sherwood

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