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Intramolecular hydrogen bonds in 3-diethylaminomethyl-5-R-salicylic aldehydes
Authors:A. Szady-Chemieniecka   Z. Rozwadowski   T. Dziembowska   E. Grech   G. Wojciechowski  B. Brzezinski
Affiliation:A. Szady-Che"Image"mieniecka, Z. Rozwadowski, T. Dziembowska, E. Grech, G. Wojciechowski,B. Brzezinski,
Abstract:Two 3-diethylaminomethyl-5-R-salicylic aldehydes were obtained and studied in chloroform solutions by FTIR and NMR spectroscopy. The existence of an equilibrium between the structures with OHO=C and NHO intramolecular hydrogen bonds was suggested. In the case of compound 1 (R=OCH3) the OHO=C intramolecular hydrogen bond was more favorable whereas in the case of compound 2 (R=Br) the structure with the OHN intramolecular hydrogen bond was predominant.
Keywords:Intramolecular hydrogen bonds   Proton transfer   1H and 13C NMR   FTIR spectroscopy   Mannich base   Salicylic aldehyde
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