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Volumn 305, Issue , 2000, Pages 3-47

Chemical generation of excited states: The basis of chemiluminescence and bioluminescence

(1)  Mccapra, Frank a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

OXALIC ACID DERIVATIVE; OXETANE DERIVATIVE; PEROXIDE;

EID: 0033937250     PISSN: 00766879     EISSN: None     Source Type: Book Series    
DOI: 10.1016/s0076-6879(00)05475-6     Document Type: Review
Times cited : (65)

References (108)
  • 5
    • 0011527043 scopus 로고
    • (A. A. Frimer, ed.), CRC Press, Boca Raton, FL
    • T. Wilson, in "Singlet Oxygen" (A. A. Frimer, ed.), Vol. II, 37. CRC Press, Boca Raton, FL, 1985.
    • (1985) Singlet Oxygen , vol.2 , pp. 37
    • Wilson, T.1
  • 10
    • 12944330523 scopus 로고
    • (A. Hassner, ed.), Wiley, New York
    • W. Adam, in "Small Ring Heterocycles" (A. Hassner, ed.), Part 3, p. 232. Wiley, New York, 1983.
    • (1983) Small Ring Heterocycles , Issue.3 PART , pp. 232
    • Adam, W.1
  • 18
    • 84989714754 scopus 로고
    • (W. D. McElroy and B. Glass, eds.), Johns Hopkins Press, Baltimore
    • H. Linschitz, in "Light and Life" (W. D. McElroy and B. Glass, eds.), p. 173. Johns Hopkins Press, Baltimore, 1961.
    • (1961) Light and Life , pp. 173
    • Linschitz, H.1
  • 19
    • 85031583287 scopus 로고    scopus 로고
    • note
    • The tendency of peroxides to undergo chain decomposition reactions in the presence of amines and other electron donors is well known.
  • 21
    • 85031589641 scopus 로고    scopus 로고
    • note
    • The chemiluminescent decomposition of simple dioxetanes such as tetramethyldioxetane is not usually catalyzed by fluorescent activators. In the present case, the aromatic rings may be responsible for complex formation with the added aromatic hydrocarbon, leading to unexpected catalytic decomposition.
  • 34
    • 0000876521 scopus 로고
    • In a further refinement, E. H. White, D. F. Roswell, A. C. Dupont, and A. A. Wilson, J. Am. Chem. Soc. 109, 5189 (1987) interpret the reactions of acridine esters with hydrogen peroxide as forming the excited state within a transition state, without the full formation of the dioxetanone intermediate.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 5189
    • White, E.H.1    Roswell, D.F.2    Dupont, A.C.3    Wilson, A.A.4
  • 36
    • 84980188395 scopus 로고
    • E. H. White and M. J. C. Harding, Photochem. Photobiol. 4, 1129 (1965). These authors concluded independently that a dioxetane provided the best explanation for the chemilumi-nescence of the compounds they were studying.
    • (1965) Photochem. Photobiol. , vol.4 , pp. 1129
    • White, E.H.1    Harding, M.J.C.2
  • 50
    • 0001356667 scopus 로고
    • Errata J. Am. Chem. Soc. 93, 1828 (1971)
    • H. E. O'Neal and W. H. Richardson, J. Am. Chem. Soc. 92, 6553 (1970). Errata J. Am. Chem. Soc. 93, 1828 (1971).
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 6553
    • O'Neal, H.E.1    Richardson, W.H.2
  • 56
    • 85031581948 scopus 로고    scopus 로고
    • note
    • However, note that the scintillation standard used in the determination of this quantum yield gives values up to twice those obtained using an alternative, the chemiluminescence of luminol.
  • 59
    • 0003001333 scopus 로고
    • (J. G. Burr, ed.), Dekker, New York
    • A. G. Mohan, in "Chemi- and Bioluminescence" (J. G. Burr, ed.), p. 245. Dekker, New York, 1985.
    • (1985) Chemi- and Bioluminescence , pp. 245
    • Mohan, A.G.1
  • 68
    • 12944262908 scopus 로고
    • (M. J. Cormier, D. M. Hercules, and J. Lee, eds.), Plenum Press, New York
    • T. Goto, M. Isobe, and K. Ienaga, in "Chemiluminescence and Bioluminescence" (M. J. Cormier, D. M. Hercules, and J. Lee, eds.), p. 492. Plenum Press, New York, 1973.
    • (1973) Chemiluminescence and Bioluminescence , pp. 492
    • Goto, T.1    Isobe, M.2    Ienaga, K.3
  • 70
    • 85031589753 scopus 로고
    • D.Phil. Thesis, University of Sussex
    • K. A. Zaklika, D.Phil. Thesis, University of Sussex, 1976.
    • (1976)
    • Zaklika, K.A.1
  • 71
    • 85031595840 scopus 로고
    • D.Phil. Thesis, University of Sussex
    • M. Taheri-Kadkhoda, D.Phil. Thesis, University of Sussex, 1986.
    • (1986)
    • Taheri-Kadkhoda, M.1
  • 87
    • 85031592043 scopus 로고    scopus 로고
    • note
    • The molecular species in this case includes, of course, the concept of an enzyme-bound emitter.
  • 93
    • 0005177970 scopus 로고
    • (J. G. Burr, ed.), Dekker, New York
    • J. Lee, in "Chemi- and Bioluminescence" (J. G. Burr, ed.), p. 401. Dekker, New York, 1985.
    • (1985) Chemi- and Bioluminescence , pp. 401
    • Lee, J.1
  • 98
    • 0039833468 scopus 로고
    • (D. E. Edmondson and D. B. McCormick, eds.), De Gruyter, New York
    • S.-C. Tu, L.-H. Wang, and Y. Yu, in "Flavins and Flavoproteins" (D. E. Edmondson and D. B. McCormick, eds.), p. 539. De Gruyter, New York, 1987.
    • (1987) Flavins and Flavoproteins , pp. 539
    • Tu, S.-C.1    Wang, L.-H.2    Yu, Y.3
  • 106
    • 85031584921 scopus 로고    scopus 로고
    • note
    • It may be objected that we know that the addition of peroxides in the presence of the luciferase is to the 4a and not the 10a position. However, inspection of the reactivity at either site shows that they are equivalent from the point of view of peroxide adducts. The 10a system was chosen for the chemiluminescence model reaction because only these adducts are fluorescent in free solution.


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