scholarly journals Ion pair formation via photoinduced proton transfer in excited hydroxynaphthalimide-N-methylimidazole hydrogen bonded complex: effect of temperature and viscosity on dual fluorescence

2001 ◽  
Vol 3 (8) ◽  
pp. 1459-1464 ◽  
Author(s):  
László Biczók ◽  
Pierre Valat ◽  
Ve´ronique Wintgens
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.


2018 ◽  
Vol 47 (16) ◽  
pp. 5850-5859 ◽  
Author(s):  
Sandra Pérez ◽  
Pablo J. Sanz Miguel ◽  
Ramón Macías

A proton tautomerism is revealed to control ion-pair formation and proton transfer between a Proton-Sponge cation, [HPS]+, and a 10-vertex decaborane anion, [nido-B10H13]−.


1985 ◽  
Vol 178 ◽  
pp. 189-195 ◽  
Author(s):  
M. Puttemans ◽  
L. Dryon ◽  
D.L. Massart

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