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Kinetic and mechanistic investigatio...

Boston University.

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Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound./
作者:	Rowe, Gerard T.
面頁冊數:	287 p.
附註:	Adviser: John P. Caradonna.
Contained By:	Dissertation Abstracts International69-10B.
標題:	Chemistry, Inorganic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3334561
ISBN:	9780549874249

Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound.
Rowe, Gerard T.

Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound. - 287 p.

Adviser: John P. Caradonna.

Thesis (Ph.D.)--Boston University, 2009.

Low-temperature stopped-flow electronic spectroscopy was utilized to resolve the intermediates formed in the reaction of a diiron(II) compound, Fe2(H2Hbamb)2(N-MeIm)2 (H 4HBamb = 2,3-bis(2-hydroxybenzamido)dimethylbutane), 1, with the oxygen-atom donors 2,6-dimethyliodosylbenzene and p-cyanodimethylaniline N-oxide and the mechanistic probe hydroperoxide 2-methyl-1-phenylprop-2-yl hydroperoxide (MPPH). Previous studies showed that 1 is capable of catalytically oxidizing cyclohexane to cyclohexanol (300 turnovers) via a pathway involving the heterolytic cleavage of the O-O bond of MPPH (>98% peroxide utilization). We now report intimate details of the formation of the reactive intermediate and its subsequent decay in the absence of substrates. The reaction, which is independent of the nature of the oxidant, proceeds via three consecutive steps assigned as (i) oxygen-atom transfer to one of the iron centers of 1 to form an FeIV=O species, 2, (ii) ligand rearrangement to 3, and (iii) internal collapse of the terminal oxo group to generate a diferric, mu-oxo species, 4. Assignment of the second step as a ligand rearrangement was corroborated by stopped-flow spectroscopic studies of the one-electron oxidation of diferrous 1, which is also known to undergo ligand rearrangement upon the formation of the [Fe II FeIII] mixed-valent complex. The role of the ligand reorganization in the energetic profile for the formation of the catalytically competent intermediate is discussed, along with the potential biological significance of the internal conversion of the active oxidant to the inert, mu-oxo diiron(III) dimer, 4.

ISBN: 9780549874249Subjects--Topical Terms:

517253
Chemistry, Inorganic.

Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound.
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245 1 0 $a Kinetic and mechanistic investigations into the workings of a binuclear nonheme iron monooxygenase model compound.
300 $a 287 p.
500 $a Adviser: John P. Caradonna.
500 $a Source: Dissertation Abstracts International, Volume: 69-10, Section: B, page: 6097.
502 $a Thesis (Ph.D.)--Boston University, 2009.
520 $a Low-temperature stopped-flow electronic spectroscopy was utilized to resolve the intermediates formed in the reaction of a diiron(II) compound, Fe2(H2Hbamb)2(N-MeIm)2 (H 4HBamb = 2,3-bis(2-hydroxybenzamido)dimethylbutane), 1, with the oxygen-atom donors 2,6-dimethyliodosylbenzene and p-cyanodimethylaniline N-oxide and the mechanistic probe hydroperoxide 2-methyl-1-phenylprop-2-yl hydroperoxide (MPPH). Previous studies showed that 1 is capable of catalytically oxidizing cyclohexane to cyclohexanol (300 turnovers) via a pathway involving the heterolytic cleavage of the O-O bond of MPPH (>98% peroxide utilization). We now report intimate details of the formation of the reactive intermediate and its subsequent decay in the absence of substrates. The reaction, which is independent of the nature of the oxidant, proceeds via three consecutive steps assigned as (i) oxygen-atom transfer to one of the iron centers of 1 to form an FeIV=O species, 2, (ii) ligand rearrangement to 3, and (iii) internal collapse of the terminal oxo group to generate a diferric, mu-oxo species, 4. Assignment of the second step as a ligand rearrangement was corroborated by stopped-flow spectroscopic studies of the one-electron oxidation of diferrous 1, which is also known to undergo ligand rearrangement upon the formation of the [Fe II FeIII] mixed-valent complex. The role of the ligand reorganization in the energetic profile for the formation of the catalytically competent intermediate is discussed, along with the potential biological significance of the internal conversion of the active oxidant to the inert, mu-oxo diiron(III) dimer, 4.
520 $a Heterolytic O-O bond cleavage of MPPH by 1 results in the formation of intermediate species whose UV/vis spectra and kinetic behavior suggest parallel reactivity to that seen in reactions with oxygen atom donor molecules. Kinetic analysis of the reaction with MPPH indicates that there is a preequilibrium binding step that manifests as saturation behavior in peroxide concentration.
520 $a Under cryogenic stopped-flow conditions, addition of p-CN-DMANO to the non-heme mixed-valence (FeII, FeIII), [Fe2(H2Hbamb)2(N-MeIm)2] +, 5 results in the rapid formation of a high-valent species, 6, assigned as a mixed-valence (FeIII, FeIV(O)) compound. Addition of 2,4,6-tri-tert-butylphenol to the reaction mixture affords production of the corresponding phenoxyl radical species resulting from the two-step oxidation of 1.9(1) equivalents of 2,4,6-tri- tert-butylphenol by the high-valent iron species.
590 $a School code: 0017.
650 4 $a Chemistry, Inorganic. $3 517253
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710 2 $a Boston University. $3 1017454
773 0 $t Dissertation Abstracts International $g 69-10B.
790 $a 0017
790 1 0 $a Caradonna, John P., $e advisor
791 $a Ph.D.
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