• Ruthenium(III)-edta type complexes for DNA-metallation

    • Fulltext

       

        Click here to view fulltext PDF


      Permanent link:
      https://www.ias.ac.in/article/fulltext/jcsc/111/03/0437-0442

    • Keywords

       

      Ruthenium(III)-edta; DNA-bases; nucleosides; nucleotides; DNA-metallation; kinetics

    • Abstract

       

      Interactions of [RuIII(edta)(H2O)] (edta=ethylenediaminetetraacetate) with DNA related molecules L (L=DNA-bases, nucleosides, nucleotides and single strand calf-thymus DNA) were studied by spectrophotometric, electrochemical and kinetic methods. The spectral features of substituted product [RuIII(edta)L] complexes were characterized by a strong ligand-to-metal charge transfer band in the UV region (293–310 nm). However, a blue colour is developed (λmax=582 nm) at highpH (>7.0) for L=GMP (guanosine-5′-monophosphate) Dissociation of N1-H proton of purine portion of coordinated GMP is suggested to promote ligand-to-metal charge band at lower energy (visible) region. The E1/2 values corresponding to RuIII/RuII redox couple for [RuIII(edta)L) complexes are in the range −0.28 to −0.12 V (vs SCE). Formation kinetics of [RuIII(edta)L] was studied using stopped-flow methods. Comparing the reactivity of [RuIII(edta)H2O)] with L in terms of spectral, electrochemical and kinetic data, it is proposed that binding of DNA with Ru(III)-edta complex takes place through adenine base unit.

    • Author Affiliations

       

      Debabrata Chatterjee1

      1. Chemistry Section, Central Mechanical Engineering Research Institute, Durgapur - 713 209, India
    • Dates

       
  • Journal of Chemical Sciences | News

© 2021-2022 Indian Academy of Sciences, Bengaluru.