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Non-standard base pairing and stacked structures in methyl xanthine clusters†
Michael P. Callahan,Zsolt Gengeliczki,Nathan Svadlenak,Haydee Valdes,Pavel Hobza,Mattanjah S. de Vries
Physical Chemistry Chemical Physics Pub Date : 03/17/2008 00:00:00 , DOI:10.1039/B719874D
Abstract

We present resonant two-photon ionization and IR–UV double resonance spectra of methylated xanthine derivatives including 7-methylxanthine dimer and theobromine dimer seeded in a supersonic jet by laser desorption. For 7-methylxanthine, theophylline and theobromine monomer we assign the lowest energy tautomer based on comparison with IR–UV double resonance spectra and calculated IR frequencies. For the 7-methylxanthine dimer, we observe hydrogen bonding on the N3H position suggesting 3 possible combinations, one that is reverse Watson–Crick type and two that are reverse Hoogsteen type. For the theobromine dimer, we observe a stacked structure. For trimethylxanthine dimers we infer a stacked structure as well.

Graphical abstract: Non-standard base pairing and stacked structures in methyl xanthine clusters
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