Acidity of ortho-substituted benzoic acids: an infrared and theoretical study of the intramolecular hydrogen bonds

2006 ◽  
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pp. 2003-2011 ◽  
Author(s):  
Pavel Fiedler ◽  
Stanislav Böhm ◽  
Jiří Kulhánek ◽  
Otto Exner
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pp. 1304-1315 ◽  
Author(s):  
Tzvetan Mihaylov ◽  
Ivelina Georgieva ◽  
Günther Bauer ◽  
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Ilia Manolov ◽  
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Vol 40 (3) ◽  
pp. 2730-2740 ◽  
Author(s):  
Reinaldo Pis-Diez ◽  
Gustavo A. Echeverría ◽  
Oscar E. Piro ◽  
Jorge L. Jios ◽  
Beatriz S. Parajón-Costa

The potassium salt of the Schiff base derived from o-vanillin and taurine is involved in enol-imine (I) and keto-amine (II) tautomerism. Both tautomeric forms coexist in the crystal and they are stabilized by strong O–H⋯N and O⋯H–N intramolecular hydrogen bonds.


2010 ◽  
Vol 114 (27) ◽  
pp. 8961-8970 ◽  
Author(s):  
Catalina Soriano-Correa ◽  
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Vol 145 ◽  
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Author(s):  
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Elisa Leyva ◽  
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Vol 774 (1-3) ◽  
pp. 1-6 ◽  
Author(s):  
Mingqiang Huang ◽  
Weijun Zhang ◽  
Yong yang ◽  
Zhenya Wang ◽  
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...  

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