Characterization of Fluxional Hydrogen-Bonded Complexes of Acetic Acid and Acetate by NMR:  Geometries and Isotope and Solvent Effects

2004 ◽  
Vol 126 (17) ◽  
pp. 5621-5634 ◽  
Author(s):  
Peter M. Tolstoy ◽  
Parwin Schah-Mohammedi ◽  
Sergei N. Smirnov ◽  
Nikolai S. Golubev ◽  
Gleb S. Denisov ◽  
...  
1989 ◽  
Vol 18 (5) ◽  
pp. 471-480 ◽  
Author(s):  
J. N. Spencer ◽  
A. Grushow ◽  
T. F. Ganunis ◽  
K. N. Allott ◽  
S. P. Kneizys ◽  
...  

1986 ◽  
Vol 90 (18) ◽  
pp. 4443-4447 ◽  
Author(s):  
J. N. Spencer ◽  
K. J. Modarress ◽  
W. L. Nachlis ◽  
J. W. Hovick

2004 ◽  
Vol 700 (1-3) ◽  
pp. 3-12 ◽  
Author(s):  
Nikolai S. Golubev ◽  
Peter M. Tolstoy ◽  
Sergei N. Smirnov ◽  
Gleb S. Denisov ◽  
Hans-Heinrich Limbach

2015 ◽  
Vol 2015 ◽  
pp. 1-14
Author(s):  
Jeremy R. Wolf

The preparation and characterization of laterally substituted 4-alkoxy-stilbazoles, 4-alkoxy-benzoic acids, and 4-alkoxy phenols and hydrogen bonded heterodimeric mixtures of these compounds are reported. Lateral substitution has a minimal effect on the ring electronics of 4-alkoxy benzoic acids and 4-alkoxy phenols; however the ring electronics of stilbazole units is extremely sensitive to lateral substitution. While lateral substitution is an effective technique for lowering the melting points of both hydrogen bonded complexes and their individual components, its effect on the electronics of stilbazoles and steric disruption of both intermolecular hydrogen bonding and molecular packing in the solid state disrupts the formation of liquid crystalline phases in both the individual components and hydrogen bonded complexes.


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