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Volumn 15, Issue 39, 2009, Pages 10182-10198

Factors that affect the nature of the final oxidation products in "peroxoshunt" reactions of iron-porphyrin complexes

Author keywords

Iron; Oxidation; Porphyrinoids, peroxo ligands; Solvent effects; UV Vis spectroscopy

Indexed keywords

AQUEOUS ACETONITRILE; AQUEOUS METHANOL; BASIC CONDITIONS; BOND CLEAVAGES; CHLOROPEROXYBENZOIC ACID; ENVIRONMENTAL CHANGE; IRON-PORPHYRIN; LOW TEMPERATURES; LOW-TO-HIGH; OXIDATION PRODUCTS; OXOIRON; PH RANGE; PORPHYRIN CATIONS; PORPHYRIN COMPLEXES; PORPHYRINOIDS, PEROXO LIGANDS; REACTION CONDITIONS; REACTION MEDIUM; SOLVENT EFFECTS; SPECTRAL CHANGE; SPECTROSCOPIC TECHNIQUE; TETRAKIS; TRIMETHYL; TWO-ELECTRON REDUCTION; UV/VIS SPECTROSCOPY;

EID: 70349653332     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900453     Document Type: Article
Times cited : (20)

References (78)
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    • 2] (HOR = methanol or water) is only of minor importance with regard to the interpretation of the experimental results presented herein
    • 2] (HOR = methanol or water) is only of minor importance with regard to the interpretation of the experimental results presented herein.
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    • IIIOOC(O)Ar] intermediate presumably exists as a five-coordinate high-spin species in the deprotonated form at pH > 4 (see ref. [10])
    • IIIOOC(O)Ar] intermediate presumably exists as a five-coordinate high-spin species in the deprotonated form at pH > 4 (see ref. [10]).
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    • 3] were unsuccessful probably due to the very short life-time of the complex and the small fraction of this intermediate formed under the selected reaction conditions
    • 3] were unsuccessful probably due to the very short life-time of the complex and the small fraction of this intermediate formed under the selected reaction conditions.
  • 76
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    • III(TMPS)] complex in water/acetonitrile are occupied by water molecules
    • III(TMPS)] complex in water/acetonitrile are occupied by water molecules.
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    • IV(O)(X)] in acetonitrile; another possibility is that m-CBA, the reduced form of m-CPBA, can act as an axial ligand (see ref. [2d])
    • IV(O)(X)] in acetonitrile; another possibility is that m-CBA, the reduced form of m-CPBA, can act as an axial ligand (see ref. [2d]).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.