The Tautomeric Equilibria of Thio-Analogues of Nucleic Acid Bases. Part 1. 2-Thiouracil: Background, Preparation of Model Compounds, and Gas Phase Proton Affinities

Abstract

The preparation is reported of all four of the mono-alkyl derivatives of 2-thiouracil, and of four of the six possible dialkyl derivatives required as models for study of the tautomeric equilibria by physical methods. Gas phase proton affinities are determined using ion cyclotron resonance mass spectrometry, and used to provide quantitative estimates of individual tautomer stabilities in the vapor state. These quantitative results agree well with qualitative deductions of predominant structures for the monoalkyl derivatives from IR spectroscopy.

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Document Details

Document Type
Technical Report
Publication Date
May 11, 1989
Accession Number
ADA208017

Entities

People

  • Alan R. Katritzky
  • Gokhan Baykut
  • Kenneth C. Caster
  • Miroslaw Szafran
  • Stanislaw Rachwal

Organizations

  • University of Florida

Tags

Communities of Interest

  • Weapons Technologies

DTIC Thesaurus Topics

  • Agreements
  • Analogs
  • Chemical Synthesis
  • Chemistry
  • Column Chromatography
  • Cyclotron Resonance
  • Mass Spectrometry
  • Measurement
  • Military Research
  • Nucleic Acids
  • Phase
  • Plastic Explosives
  • Poisoning
  • Resonance
  • Silica Gels
  • Spectrometry
  • Spectroscopy

Fields of Study

  • Chemistry

Readers

  • Analytical Chemistry
  • Molecular Photonics/Laser Physics
  • Quantum Chemistry

Technology Areas

  • Biotechnology