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Published on: November 9, 2019
Coupled hydrogen-bonding interactions between beta-carboline derivatives and acetic acid
D Reyman1, F Hallwass, Simone M da Cruz Gonçalves
1University Autónoma de Madrid, Department Quimica Física Aplicada, Cantoblanco, Madrid, 28049, Spain. dolores.reyman@uam.es
Abstract:
In this work, we have analysed the tendency of two beta-carboline derivatives, harmane and norharmane, in the formation of hydrogen bonds. We obtained the (1)H and (13)C NMR spectra of different mixtures of these derivatives with acetic acid (AcOH) in CDCl(3). A cyclic 1:3 complex is proposed between harmane and AcOH, while a 1:2 complex is proposed for norharmane. Chemical shifts at temperatures between 233 and 323 K were measured: lowering the temperature produces the same effect as increasing the amount of AcOH in solution. The (13)C data confirm a delocalisation of the pi electron density towards the pyridinic ring that occurs when AcOH is added.
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