1. Electrochemical proton-coupled electron transfer processes to form neutral radicals of azaphenalenes: pKa values of protonated radicals.
- Author
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Suzuki, Hiroaki, Wada, Yuki, Usov, Pavel M., Zhu, Yiying, Chan, Bun, Hall, Lyndon A., D'Alessandro, Deanna M., Kajiwara, Atsushi, Haga, Masa-aki, and Kawano, Masaki
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RADICALS (Chemistry) , *CHARGE exchange , *BUFFER solutions , *REDUCTION potential , *DIGITAL computer simulation - Abstract
Azaphenalenes are nitrogen substituted analogues of the phenalene ring system, and their radicals have attracted significant attention because of the novel electronic and magnetic properties. In the previous study, the neutral tris(tert-butyl) 1,3-diazaphenalenyl radical has been synthesized by chemical oxidation of the parent compound with PbO 2. In this study, we focused on electrochemical proton-coupled electron transfer (PCET) process leading to the formation of neutral unsubstituted 1,3-diazaphenalenyl radical from 1,3-diazaphenalene (DAP) in solution. Additionally, this electrochemical approach was extended to study the redox behavior of newly synthesized 1,4,7-triazaphenalene (TAP) giving the access to the 1,4,7-triazaphenalenyl radical. Electrochemical oxidation potentials vs. pH plots (Pourbaix diagram) for DAP and TAP revealed that their one-electron oxidation to the corresponding neutral radicals occurred by a PCET process over a wide pH range. From the analysis of Pourbaix diagrams, the p K a values of the protonated radicals were determined to be p K a = 2.57 and 2.39 for the DAP and TAP radicals, respectively. Cyclic voltammograms of azaphenalenes in MeCN and MeCN/buffer solutions showed a characteristic ECE process, in which electrochemical oxidative dimerization took place following the electron transfer. The dimerization reaction pathway was rationalized by the digital simulations, DFT calculations and crystallization of a DAP dimer after chemical oxidation with PbO 2. The spectroscopic properties of azaphenalenes and their dimerized products were characterized by in-situ UV–Vis and EPR spectroelectrochemistry techniques. The fundamental information about the p K a and redox potentials for a series of azaphenalenes (DAP, TAP, as well as 1,3,4,6,7,9-hexaazaphenalene, HAP) could be fed back into the molecular design of redox-active conductive coordination networks based on multi-interactive ligands. [Display omitted] [ABSTRACT FROM AUTHOR]
- Published
- 2024
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