Survey of the proton affinities of adenine, cytosine, thymine and uracil dideoxyribonucleosides, deoxyribonucleosides and ribonucleosides

J Mass Spectrom. 2000 Feb;35(2):139-44. doi: 10.1002/(SICI)1096-9888(200002)35:2<139::AID-JMS921>3.0.CO;2-A.

Abstract

The kinetic method was applied to the determination of the proton affinities (PAs) of modified deoxy- and dideoxyribonucleosides. A correlation between the measured PAs and the replacement of one of the three hydroxyl groups of the ribose unit is presented. A PA scale was obtained which shows that the replacement of the primary or of one or both secondary hydroxyl groups of a ribonucleoside with a hydrogen atom induces the lowering or the enhancement of the nucleoside PA, respectively. The scale extends over a very narrow range of approximately 2 kcal mol(-1), thus demonstrating the sensitivity of the kinetic method in the evaluation of small differences in thermodynamic parameters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine Nucleotides / chemistry
  • Algorithms
  • Cytosine Nucleotides / chemistry
  • Deoxyribonucleosides / chemistry
  • Dideoxynucleosides / chemistry
  • Kinetics
  • Nucleosides / chemistry*
  • Protons
  • Ribonucleosides / chemistry
  • Spectrometry, Mass, Fast Atom Bombardment
  • Thermodynamics
  • Thymine Nucleotides / chemistry
  • Uracil Nucleotides / chemistry

Substances

  • Adenine Nucleotides
  • Cytosine Nucleotides
  • Deoxyribonucleosides
  • Dideoxynucleosides
  • Nucleosides
  • Protons
  • Ribonucleosides
  • Thymine Nucleotides
  • Uracil Nucleotides