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Volumn 25, Issue 8, 1999, Pages 789-811

Photooxidation of benzyl alcohol derivatives by oxygen, catalyzed by protonated flavin analogues

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EID: 0001562128     PISSN: 09226168     EISSN: None     Source Type: Journal    
DOI: 10.1163/156856799X00680     Document Type: Article
Times cited : (35)

References (86)
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    • (1971) Methods in Enzymology , vol.18 B , pp. 479
    • Penzer, G.R.1    Radda, G.K.2
  • 6
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    • M.A. Fox and M. Chanon (Eds.), Elsevier, Amsterdam
    • (d) S. Fukuzumi and T. Tanaka, Photoinduced Electron Transfer, Part C, M.A. Fox and M. Chanon (Eds.), Elsevier, Amsterdam, 1988, p. 636.
    • (1988) Photoinduced Electron Transfer , Issue.PART C , pp. 636
    • Fukuzumi, S.1    Tanaka, T.2
  • 7
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    • Catalysis of photochemical reactions has been reviewed; see: G.G. Wubbels, Acc. Chem. Res. 16, 285 (1983). Species which enhance the reactivity of photocatalysts may be called "co- catalysts" of photocatalysts; see: S. Fukuzumi and S. Itoh, Advances in Photochemistry, D.C. Neckers, D.H. Volma, G. von Bünau (Eds.), John Wiley, Vol. 25, 1999, in press.
    • (1983) Acc. Chem. Res. , vol.16 , pp. 285
    • Wubbels, G.G.1
  • 8
    • 0004242084 scopus 로고    scopus 로고
    • D.C. Neckers, D.H. Volma, G. von Bünau (Eds.), John Wiley, in press
    • Catalysis of photochemical reactions has been reviewed; see: G.G. Wubbels, Acc. Chem. Res. 16, 285 (1983). Species which enhance the reactivity of photocatalysts may be called "co-catalysts" of photocatalysts; see: S. Fukuzumi and S. Itoh, Advances in Photochemistry, D.C. Neckers, D.H. Volma, G. von Bünau (Eds.), John Wiley, Vol. 25, 1999, in press.
    • (1999) Advances in Photochemistry , vol.25
    • Fukuzumi, S.1    Itoh, S.2
  • 19
    • 0000395704 scopus 로고
    • S. Fukuzumi, S. Kuroda, and T. Tanaka, J. Am. Chem. Soc. 107, 3020 (1985); Chem. Lett. 417, 1375 (1984).
    • (1984) Chem. Lett. , vol.417 , pp. 1375
  • 32
    • 85034547937 scopus 로고    scopus 로고
    • note
    • The amount of hydrogen peroxide becomes smaller than that of benzaldehyde at longer irradiation time, probably because of the photodecomposition of hydrogen peroxide.
  • 33
    • 0029903531 scopus 로고    scopus 로고
    • The ab initio MO calculations indicate that N(1) is the site of protonation of flavin; see: Y.-J. Zheng and R.L. Ornstein, J. Am. Chem. Soc. 118, 9402 (1996).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9402
    • Zheng, Y.-J.1    Ornstein, R.L.2
  • 35
    • 0000443083 scopus 로고
    • Whether the substituents Cl- and Br- are electron-withdrawing or -donating are sensitive to the system; see: S. Fukuzumi and J.K. Kochi, J. Am. Chem. Soc. 103, 7240 (1981).
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 7240
    • Fukuzumi, S.1    Kochi, J.K.2
  • 43
    • 85034554449 scopus 로고    scopus 로고
    • note
    • +.
  • 45
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    • T.E. King, H.S. Mason, and M. Morrison (Eds.), University Park Press, MD
    • (b) V. Massey, G. Palmer, and D. Ballou. In: Oxidases and Related Redox Systems, T.E. King, H.S. Mason, and M. Morrison (Eds.), University Park Press, MD, 1973, p. 25.
    • (1973) Oxidases and Related Redox Systems , pp. 25
    • Massey, V.1    Palmer, G.2    Ballou, D.3
  • 58
    • 85034538351 scopus 로고    scopus 로고
    • note
    • 4, no fluorescence of flavin analogues (Fl, dFl and RFl) has been observed.
  • 67
    • 85034532049 scopus 로고    scopus 로고
    • note
    • •) may be disregarded since it is difficult to explain the selective photocatalytic oxidation (as observed in Figure 9) by such a radical chain mechanism.
  • 68
    • 85034531960 scopus 로고    scopus 로고
    • note
    • 2+ complex by a benzyl alcohol derivative has been reported (Ref. 6).
  • 73
    • 85034535487 scopus 로고    scopus 로고
    • note
    • •) is involved in the reactants or products (see Ref. 26a).
  • 74
    • 85034537436 scopus 로고    scopus 로고
    • note
    • + (0.19 V, reported in Ref. 32a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.