Benzo condensed crown ethers containing 1,8-naphthyridine or 4-pyridone units - synthesis and complex formation with organic guest molecules

1995 ◽  
Vol 337 (1) ◽  
pp. 451-455 ◽  
Author(s):  
E. Weber ◽  
H.-J. K�hler
Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2571
Author(s):  
Ádám Golcs ◽  
Bálint Árpád Ádám ◽  
Viola Horváth ◽  
Tünde Tóth ◽  
Péter Huszthy

New highly lipophilic enantiopure crown ethers containing a heterocyclic unit have been synthesized. Phase transport, UV-Vis- and fluorescence spectrophotometric investigations as well as electrochemical studies on the complexation of the new macrocycles with several amine and amino acid derivatives were also carried out. Achiral amines were used for studying the structural preference of the new macrocycles. Among the studied structural features of the guest molecules, the intermolecular π-π interaction showed the most significant effect on complexation, which made the aralkylamine-type compounds the most preferable guest molecules. The studied liquid membrane-based applications and photophysical investigations showed appreciable enantiomeric recognition toward some aralkylamine model compounds with homochiral preferences. New crown ether derivatives (R,R)-2 and (S,S)-2 were successfully applied as enantioselective carrier and sensor molecules.


1986 ◽  
Vol 17 (25) ◽  
Author(s):  
P. D. J. GROOTENHUIS ◽  
J. W. H. M. UITERWIJK ◽  
D. N. REINHOUDT ◽  
C. J. VAN STAVEREN ◽  
E. J. R. SUDHOELTER ◽  
...  

2008 ◽  
Vol 38 (2) ◽  
pp. 209-217 ◽  
Author(s):  
Hans-Jürgen Buschmann ◽  
Radu-Cristian Mutihac ◽  
Eckhard Schollmeyer

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