BRANDON J BAYARD
Articles written in Journal of Chemical Sciences
Volume 133 All articles Published: 28 June 2021 Article ID 0065
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.
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.
Volume 134, 2022
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