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Volumn 9, Issue 10, 2003, Pages 2347-2358

A non-radical mechanism for methane hydroxylation at the diiron active site of soluble methane monooxygenase

Author keywords

Alkane hydroxylation; C H bond activation; Density functional calculations; Kinetic isotope effect; Methane monooxygenase

Indexed keywords

CATALYSIS; CHEMICAL BONDS; HYDROXYLATION; IRON; METHANOL;

EID: 0037495952     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200204269     Document Type: Article
Times cited : (39)

References (165)
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    • note
    • 2) value for the coordinatively saturated diiron complex in the broken-symmetry singlet state is 2.07. In general, broken-symmetry calculations are significantly spin-contaminated, but spin contamination is a necessary condition for broken-symmetry calculations. If a broken-symmetry wave function has no spin contamination, we obtain the symmetric one, the spin-restricted solution.
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    • note
    • -1 above that in the nonet state.
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    • note
    • B).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.