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    • Abstract

       

      The synthesis and initial spectroscopic characterization of a phosphorus(V) octaethylporphyrinnitroxideadduct is reported. The nitroxide (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) is axially andcovalently bound to the phosphorus porphyrin (PPor+) to give the studied PPor+-TEMPO conjugate. Thecomplex allows the influence of the type of bonding and geometry of the central element in the porphyrin onthe excited state dynamics to be investigated. In addition, the high oxidation potential of the PPor+ 1.35 V vsSCE means that it is a strong oxidant in its excited state and is energetically well-placed to allow chargetransfer (CT) from TEMPO to PPor+ to occur. Cyclic voltammetry data and DFT computations show that theCT state is the lowest excited state, lying well below the excited sing-doublet and trip-quartet states of thecomplex. Time-resolved optical data show that the presence of the bound nitroxide leads to a large decreasein the excited state lifetime in acetonitrile, suggesting that rapid charge separation and recombination occurs.However, transient EPR (TREPR) data reveal that the trip-quartet state is also populated and that emissivespin polarization is generated in the ground state at room temperature, consistent with radical-quartet pairinteractions analogous to the radical-triplet pair mechanism. At low temperature, the TREPR data show thatthe trip-quartet state is formed with strong absorptive net polarization. The shape of the spectrum providesevidence of significant dynamics in the excited state probably due to reversible transitions between thethermally accessible quartet and doublet states.

    • Graphical Abstract

       

      Synopsis: Spectroscopic studies of a phosphorus (V) porphyrin with an axial covalently bound TEMPO radical reveal different relaxation pathways following light excitation. Rapid deactivation of the excited sing-doublet state populates the trip-doublet and trip-quartet states as well as the CT state generated by oxidation of the radical by the excited porphyrin.

    • Author Affiliations

       

      PRASHANTH K PODDUTOORI1 NOAH HOLZER1 BRANDON J BAYARD1 YURI E KANDRASHKIN2 GARY LIM3 FRANCIS D’SOUZA3 ART VAN DER EST4

      1. Department of Chemistry & Biochemistry, University of Minnesota Duluth, 1038 University Drive, Duluth, Minnesota 55812, USA
      2. Zavoisky Physical-Technical Institute, FRC Kazan Scientific Center of RAS, Sibirsky Tract 10/7, Kazan 420029, Russian Federation
      3. Department of Chemistry, University of North Texas, 1155 Union Circle, # 305070, Denton, Texas 76203-5017, USA
      4. Department of Chemistry, Brock University, 1812 Sir Isaac Brock Way, St. Catharines, ON L2S 3A1, Canada
    • Dates

       
  • Journal of Chemical Sciences | News

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