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- W2023275711 abstract "We describe the synthesis and dioxygen reactivity of diiron(II) tetracarboxylate complexes [Fe(2)(mu-O(2)CAr(Tol))(2)(O(2)CAr(Tol))(2)(N,N-Me(2)en)(2)] (2) and [Fe(2)(mu-O(2)CAr(Tol))(2)(O(2)CAr(Tol))(2)(N,N-Bn(2)en)(2)] (6), where Ar(Tol)CO(2)(-) = 2,6-di(p-tolyl)benzoate. These complexes were prepared as models for the diiron(II) center in the hydroxylase component of soluble methane monooxygenase (MMOH). Compound 6 reacts with dioxygen to afford PhCHO in approximately 60(5)% yield, following oxidative N-dealkylation of the pendant benzyl group on the diamine ligand. The diiron(III) complex [Fe(2)(mu-OH)(2)(mu-O(2)CAr(Tol))(O(2)CAr(Tol))(3)(N-Bnen)(N,N-Bn(2)en)] (8) was isolated from the reaction mixture. The 4.2 K Mössbauer spectrum of 8 displays a single quadrupole doublet with parameters delta = 0.48(2) mm s(-1) and Delta E(Q) = 0.61(2) mm s(-1). The [Fe(2)(mu-OH)(2)(mu-O(2)CR)](3+) core structure in 8 matches that of the fully oxidized form of MMOH. The conversion of 6 to 8 closely parallels the chemistry of MMOH in which an O(2)-derived oxygen atom is inserted into the C-H bond of methane. Several reaction pathways are considered to account for this novel chemical transformation, and these are compared with mechanistic frameworks previously developed for related cytochrome P450 and copper(I) dioxygen chemistry." @default.
- W2023275711 created "2016-06-24" @default.
- W2023275711 creator A5032470300 @default.
- W2023275711 creator A5034625027 @default.
- W2023275711 date "2002-01-31" @default.
- W2023275711 modified "2023-10-17" @default.
- W2023275711 title "Synthetic Analogue of the {Fe<sub>2</sub>(μ-OH)<sub>2</sub>(μ-O<sub>2</sub>CR)}<sup>3+</sup> Core of Soluble Methane Monooxygenase Hydroxylase via Synthesis and Dioxygen Reactivity of Carboxylate-Bridged Diiron(II) Complexes" @default.
- W2023275711 cites W1963819988 @default.
- W2023275711 cites W1964906367 @default.
- W2023275711 cites W1968286233 @default.
- W2023275711 cites W1969868637 @default.
- W2023275711 cites W1971230402 @default.
- W2023275711 cites W1971302449 @default.
- W2023275711 cites W1974268087 @default.
- W2023275711 cites W1975262546 @default.
- W2023275711 cites W1977708744 @default.
- W2023275711 cites W1979646736 @default.
- W2023275711 cites W1979692587 @default.
- W2023275711 cites W1980290845 @default.
- W2023275711 cites W1981091472 @default.
- W2023275711 cites W1981335245 @default.
- W2023275711 cites W1981704948 @default.
- W2023275711 cites W1983514748 @default.
- W2023275711 cites W1984964768 @default.
- W2023275711 cites W1987642374 @default.
- W2023275711 cites W1991324143 @default.
- W2023275711 cites W1991354940 @default.
- W2023275711 cites W1997254796 @default.
- W2023275711 cites W1998963892 @default.
- W2023275711 cites W2000466466 @default.
- W2023275711 cites W2004860446 @default.
- W2023275711 cites W2006929679 @default.
- W2023275711 cites W2009258401 @default.
- W2023275711 cites W2011607516 @default.
- W2023275711 cites W2017596140 @default.
- W2023275711 cites W2021010920 @default.
- W2023275711 cites W2025480886 @default.
- W2023275711 cites W2025703072 @default.
- W2023275711 cites W2026336405 @default.
- W2023275711 cites W2027411151 @default.
- W2023275711 cites W2027927112 @default.
- W2023275711 cites W2028291957 @default.
- W2023275711 cites W2028462347 @default.
- W2023275711 cites W2028980161 @default.
- W2023275711 cites W2031529232 @default.
- W2023275711 cites W2034672440 @default.
- W2023275711 cites W2036646206 @default.
- W2023275711 cites W2039616951 @default.
- W2023275711 cites W2040299058 @default.
- W2023275711 cites W2044428152 @default.
- W2023275711 cites W2050342005 @default.
- W2023275711 cites W2055283831 @default.
- W2023275711 cites W2058259904 @default.
- W2023275711 cites W2059426878 @default.
- W2023275711 cites W2060972467 @default.
- W2023275711 cites W2061146825 @default.
- W2023275711 cites W2061332485 @default.
- W2023275711 cites W2063965798 @default.
- W2023275711 cites W2065566485 @default.
- W2023275711 cites W2065793699 @default.
- W2023275711 cites W2068431139 @default.
- W2023275711 cites W2070458808 @default.
- W2023275711 cites W2072336629 @default.
- W2023275711 cites W2076421149 @default.
- W2023275711 cites W2077749836 @default.
- W2023275711 cites W2077934271 @default.
- W2023275711 cites W2079487076 @default.
- W2023275711 cites W2080488356 @default.
- W2023275711 cites W2080624600 @default.
- W2023275711 cites W2081298460 @default.
- W2023275711 cites W2082840768 @default.
- W2023275711 cites W2083902841 @default.
- W2023275711 cites W2084919208 @default.
- W2023275711 cites W2088034681 @default.
- W2023275711 cites W2088645007 @default.
- W2023275711 cites W2091086834 @default.
- W2023275711 cites W2092196805 @default.
- W2023275711 cites W2094187872 @default.
- W2023275711 cites W2094890326 @default.
- W2023275711 cites W2136333672 @default.
- W2023275711 cites W2151439302 @default.
- W2023275711 cites W2166060486 @default.
- W2023275711 cites W2576034638 @default.
- W2023275711 cites W2949946827 @default.
- W2023275711 cites W2950768853 @default.
- W2023275711 cites W2950948791 @default.
- W2023275711 cites W2951236169 @default.
- W2023275711 cites W2953305798 @default.
- W2023275711 cites W3138096963 @default.
- W2023275711 cites W3139480402 @default.
- W2023275711 doi "https://doi.org/10.1021/ic011008s" @default.
- W2023275711 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11849083" @default.
- W2023275711 hasPublicationYear "2002" @default.
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