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Volumn 120, Issue 12, 1998, Pages 2880-2889

Electron transfer mechanism of organocobalt porphyrins. Site of electron transfer, migration of organic groups, and cobalt-carbon bond energies in different oxidation states

Author keywords

[No Author keywords available]

Indexed keywords

PORPHYRIN DERIVATIVE;

EID: 0032053481     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja973257e     Document Type: Article
Times cited : (58)

References (68)
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    • note
    • 3+] when the migration is always the rate-determining step.
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    • A similar conclusion was made for a phenyl σ-bonded cobalt corrole, (OEC)Co(Ph), where OEC is the trianion of 2,3,7,8-12,13,17,18-octaethylcorrole; (OEC)Co(Ph) can best be represented as a resonance hybrid between a cobalt(III) π radical cation and a cobalt(IV) corrole, see: Will, S.; Lex, J.; Vogel, E.; Adamian, V. A.; Van Caemelbecke, E.; Kadish, K. M. Inorg. Chem. 1996, 35, 5577.
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    • The ESR spectra of low spin cobalt(II) complexes have been well-characterized in frozen media but cannot be detected in solution because of their short spin-lattice relaxation time, see: Walker, F. A. J. Am. Chem. Soc. 1970, 92, 4235. Wayland, B. B.; Minkiewicz, J. V.; Abd-Elmageed, M. E. J. Am. Chem. Soc. 1974, 96, 2795. Wayland, B. B.; Abd-Elmageed, M. E. J. Am. Chem. Soc. 1974, 96, 4809.
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    • The ESR spectra of low spin cobalt(II) complexes have been well-characterized in frozen media but cannot be detected in solution because of their short spin-lattice relaxation time, see: Walker, F. A. J. Am. Chem. Soc. 1970, 92, 4235. Wayland, B. B.; Minkiewicz, J. V.; Abd-Elmageed, M. E. J. Am. Chem. Soc. 1974, 96, 2795. Wayland, B. B.; Abd-Elmageed, M. E. J. Am. Chem. Soc. 1974, 96, 4809.
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    • The formation of methane as a minor product in the electron-transfer oxidation of (TPP)Co(Me) is reminiscent of minor radical products produced in dealkylation of alkylcobalt(III) complexes with iodine, which occurs via electron transfer from alkylcobalt(III) complexes to iodine, followed by the facile homolytic cleavage for the cobalt-carbon bond of the alkylcobalt-(IV) complexes, see: Ishikawa, K.; Fukuzumi, S.; Tanaka, T. Inorg. Chem. 1989, 28, 1661.
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    • note
    • The [Co(II)]/[TEMPO] dependence in eq 7 has been well established. See refs 32-34.
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    • The facile homolytic cleavage for the cobalt-carbon bonds of alkylcobalt(IV) complexes has been well-documented as compared to the slow cleavage of the corresponding alkylcobalt(III) complexes, which requires thermal or photochemical activation, see: Ishikawa, K.; Fukuzumi, S.; Goto, T.; Tanaka, T. J. Am. Chem. Soc. 1990, 112, 1577. Fukuzumi, S.; Ishikawa, K.; Tanaka, T. Organametallics 1987, 6, 358. Ishikawa, K.; Fukuzumi, S.; Tanaka, T. Bull. Chem. Soc. Jpn. 1987, 60, 563. Fukuzumi, S.; Kitano, T.; Ishikawa, M.; Matsuda, Y. Chem. Phys. 1993, 176, 337.
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    • The facile homolytic cleavage for the cobalt-carbon bonds of alkylcobalt(IV) complexes has been well-documented as compared to the slow cleavage of the corresponding alkylcobalt(III) complexes, which requires thermal or photochemical activation, see: Ishikawa, K.; Fukuzumi, S.; Goto, T.; Tanaka, T. J. Am. Chem. Soc. 1990, 112, 1577. Fukuzumi, S.; Ishikawa, K.; Tanaka, T. Organametallics 1987, 6, 358. Ishikawa, K.; Fukuzumi, S.; Tanaka, T. Bull. Chem. Soc. Jpn. 1987, 60, 563. Fukuzumi, S.; Kitano, T.; Ishikawa, M.; Matsuda, Y. Chem. Phys. 1993, 176, 337.
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    • The facile homolytic cleavage for the cobalt-carbon bonds of alkylcobalt(IV) complexes has been well-documented as compared to the slow cleavage of the corresponding alkylcobalt(III) complexes, which requires thermal or photochemical activation, see: Ishikawa, K.; Fukuzumi, S.; Goto, T.; Tanaka, T. J. Am. Chem. Soc. 1990, 112, 1577. Fukuzumi, S.; Ishikawa, K.; Tanaka, T. Organametallics 1987, 6, 358. Ishikawa, K.; Fukuzumi, S.; Tanaka, T. Bull. Chem. Soc. Jpn. 1987, 60, 563. Fukuzumi, S.; Kitano, T.; Ishikawa, M.; Matsuda, Y. Chem. Phys. 1993, 176, 337.
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    • The facile homolytic cleavage for the cobalt-carbon bonds of alkylcobalt(IV) complexes has been well-documented as compared to the slow cleavage of the corresponding alkylcobalt(III) complexes, which requires thermal or photochemical activation, see: Ishikawa, K.; Fukuzumi, S.; Goto, T.; Tanaka, T. J. Am. Chem. Soc. 1990, 112, 1577. Fukuzumi, S.; Ishikawa, K.; Tanaka, T. Organametallics 1987, 6, 358. Ishikawa, K.; Fukuzumi, S.; Tanaka, T. Bull. Chem. Soc. Jpn. 1987, 60, 563. Fukuzumi, S.; Kitano, T.; Ishikawa, M.; Matsuda, Y. Chem. Phys. 1993, 176, 337.
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