Formation and High Reactivity of the anti-Dioxo Form of High-Spin μ-Oxodioxodiiron(IV) as the Active Species That Cleaves Strong C-H Bonds

Masahito Kodera, Shin Ishiga, Tomokazu Tsuji, Katsutoshi Sakurai, Yutaka Hitomi, Yoshihito Shiota, P. K. Sajith, Kazunari Yoshizawa, Kaoru Mieda, Takashi Ogura

Research output: Contribution to journalArticle

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Abstract

Recently, it was shown that μ-oxo-μ-peroxodiiron(III) is converted to high-spin μ-oxodioxodiiron(IV) through O-O bond scission. Herein, the formation and high reactivity of the anti-dioxo form of high-spin μ-oxodioxodiiron(IV) as the active oxidant are demonstrated on the basis of resonance Raman and electronic-absorption spectral changes, detailed kinetic studies, DFT calculations, activation parameters, kinetic isotope effects (KIE), and catalytic oxidation of alkanes. Decay of μ-oxodioxodiiron(IV) was greatly accelerated on addition of substrate. The reactivity order of substrates is toluene<ethylbenzene≈cumene<trans-β-methylstyrene. The rate constants increased proportionally to the substrate concentration at low substrate concentration. At high substrate concentration, however, the rate constants converge to the same value regardless of the kind of substrate. This is explained by a two-step mechanism in which anti-μ-oxodioxodiiron(IV) is formed by syn-to-anti transformation of the syn-dioxo form and reacts with substrates as the oxidant. The anti-dioxo form is 620 times more reactive in the C-H bond cleavage of ethylbenzene than the most reactive diiron system reported so far. The KIE for the reaction with toluene/[D8]toluene is 95 at -30 °C, which the largest in diiron systems reported so far. The present diiron complex efficiently catalyzes the oxidation of various alkanes with H2O2. Strong anti oxidant: A high-spin μ-oxodioxodiiron(IV) species undergoes transformation from the syn-dioxo to the anti-dioxo form, which cleaves strong C-H bonds of alkanes. The high-spin anti-dioxodiiron(IV) species with a sterically less hindered structure (see figure) is a highly reactive and selective oxidant. These results provide insight into the high reactivity of the active species Q of soluble methane monooxygenases and the development of efficient alkane oxidation catalysts.

Original languageEnglish
Pages (from-to)5924-5936
Number of pages13
JournalChemistry - A European Journal
Volume22
Issue number17
DOIs
Publication statusPublished - Apr 18 2016

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Alkanes
Oxidants
Paraffins
Substrates
Toluene
methane monooxygenase
Isotopes
Rate constants
Oxidation
Kinetics
Ethylbenzene
Catalytic oxidation
Kinetic parameters
Discrete Fourier transforms
Methane
Chemical activation
Catalysts

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Cite this

Formation and High Reactivity of the anti-Dioxo Form of High-Spin μ-Oxodioxodiiron(IV) as the Active Species That Cleaves Strong C-H Bonds. / Kodera, Masahito; Ishiga, Shin; Tsuji, Tomokazu; Sakurai, Katsutoshi; Hitomi, Yutaka; Shiota, Yoshihito; Sajith, P. K.; Yoshizawa, Kazunari; Mieda, Kaoru; Ogura, Takashi.

In: Chemistry - A European Journal, Vol. 22, No. 17, 18.04.2016, p. 5924-5936.

Research output: Contribution to journalArticle

Kodera, Masahito ; Ishiga, Shin ; Tsuji, Tomokazu ; Sakurai, Katsutoshi ; Hitomi, Yutaka ; Shiota, Yoshihito ; Sajith, P. K. ; Yoshizawa, Kazunari ; Mieda, Kaoru ; Ogura, Takashi. / Formation and High Reactivity of the anti-Dioxo Form of High-Spin μ-Oxodioxodiiron(IV) as the Active Species That Cleaves Strong C-H Bonds. In: Chemistry - A European Journal. 2016 ; Vol. 22, No. 17. pp. 5924-5936.
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