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Volumn 133, Issue 22, 2011, Pages 8544-8551

Proton-coupled electron transfer reactions at a heme-propionate in an iron-protoporphyrin-IX model compound

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE SITE; BENZOQUINONES; BOND-DISSOCIATION FREE ENERGIES; ELECTRON TRANSFER; HEME MODELS; HEME PROPIONATES; HEME PROTEINS; IRON CENTERS; KEY COMPONENT; MODEL COMPOUND; N-METHYLIMIDAZOLE; PROPIONIC ACIDS; PROTON-COUPLED ELECTRON TRANSFER; PROTON-COUPLED ELECTRON TRANSFER REACTIONS; PROTOPORPHYRINS;

EID: 79957992397     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja201663p     Document Type: Article
Times cited : (46)

References (88)
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    • + in the same kinetic step, while PCET refers to any process affected by transfer of both electron(s) and proton(s)
    • + in the same kinetic step, while PCET refers to any process affected by transfer of both electron(s) and proton(s)
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    • See, for instance
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    • Guallar, V.1
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    • Generated using the PyMOL Molecular Graphics System, Version 1.2r3pre, Schrödinger, LLC.
    • Generated using the PyMOL Molecular Graphics System, Version 1.2r3pre, Schrödinger, LLC.
  • 33
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    • 2 is surprising. Similar changes are observed on adding 1 equiv of DBU to the bis(N-MeIm) complex of native PPIX (not esterified).
    • 2 is surprising. Similar changes are observed on adding 1 equiv of DBU to the bis(N-MeIm) complex of native PPIX (not esterified).
  • 41
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    • Reference 3, Section 5.9.
    • Reference 3, Section 5.9.
  • 46
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    • - used in this study.
    • - used in this study.
  • 49
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    • See, for instance, refs 1b, 1c, 3, 4, 15, and 25.
    • See, for instance, refs 1b, 1c, 3, 4, 15, and 25.
  • 50
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    • -) = 28.7. (3)
    • -) = 28.7. (3)
  • 55
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    • Reference 32b shows the favoring of stepwise paths at higher overall driving force. Reference 32c gives the reduction potential of compounds I and II in APX, but it is not known whether these are pure ET potentials or if they also involve proton(s).
    • Reference 32b shows the favoring of stepwise paths at higher overall driving force. Reference 32c gives the reduction potential of compounds I and II in APX, but it is not known whether these are pure ET potentials or if they also involve proton(s).
  • 73
    • 79957977092 scopus 로고    scopus 로고
    • a = 25.5 (Tp = hydrotrispyrazolylborate). (43d)
    • a = 25.5 (Tp = hydrotrispyrazolylborate). (43d)
  • 77
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    • See also ref 9, 10 and 38
    • Guallar, V.; Olsen, B. J. Inorg. Biochem. 2006, 100, 755-760. See also ref 9, 10 and 38
    • (2006) J. Inorg. Biochem. , vol.100 , pp. 755-760
    • Guallar, V.1    Olsen, B.2
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    • In;, Ed.; Academic: New York, Vol., Part B, pp; see especially p 76.
    • La Mar, G.; Walker, F. A. In The Porphyrins; Dolphin, D., Ed.; Academic: New York, 1979; Vol. 4, Part B, pp 61-157; see especially p 76.
    • (1979) The Porphyrins , vol.4 , pp. 61-157
    • La Mar, G.1    Walker, F.A.2    Dolphin, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.