메뉴 건너뛰기




Volumn 89, Issue 6, 2013, Pages 1299-1317

Efficiency of electron transfer initiated chemiluminescence

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRON TRANSPORT; LUMINESCENCE; QUANTUM THEORY;

EID: 84887403006     PISSN: 00318655     EISSN: 17511097     Source Type: Journal    
DOI: 10.1111/php.12102     Document Type: Review
Times cited : (106)

References (149)
  • 3
    • 0003922512 scopus 로고    scopus 로고
    • Prentice Hall, Upper Saddle River
    • Bruice, P. Y., (2010) Organic Chemistry. Prentice Hall, Upper Saddle River.
    • (2010) Organic Chemistry
    • Bruice, P.Y.1
  • 4
    • 84977358997 scopus 로고
    • Das Experiment: Singulettsauerstoff - Chemische Erzeugung und Chemilumineszenz
    • Adam, W., and, W. J. Baader, (1982) Das Experiment: Singulettsauerstoff- Chemische Erzeugung und Chemilumineszenz. Chem. unserer Zeit 16, 169-171.
    • (1982) Chem. Unserer Zeit , vol.16 , pp. 169-171
    • Adam, W.1    Baader, W.J.2
  • 7
    • 0000394490 scopus 로고
    • Über die Chemiluminescenz des Aminophthalsäurehydrazids
    • Albrecht, H. O., (1928) Über die Chemiluminescenz des Aminophthalsäurehydrazids. Z. Phys. Chem. 136, 321-330.
    • (1928) Z. Phys. Chem. , vol.136 , pp. 321-330
    • Albrecht, H.O.1
  • 8
    • 0003154894 scopus 로고
    • Die Chemiluminescenz der Dimethyldiacridyliumsalze
    • Gleu, K., and, W. Petsch, (1935) Die Chemiluminescenz der Dimethyldiacridyliumsalze. Angew. Chem. 48, 57-59.
    • (1935) Angew. Chem. , vol.48 , pp. 57-59
    • Gleu, K.1    Petsch, W.2
  • 9
    • 0041433568 scopus 로고
    • Untersuchungen über Hydrobenzamid, Amarin und Lophin
    • Radziszewski, B. R., (1877) Untersuchungen über Hydrobenzamid, Amarin und Lophin. Ber. Dtsch. Chem. Ges. 10, 70-75.
    • (1877) Ber. Dtsch. Chem. Ges. , vol.10 , pp. 70-75
    • Radziszewski, B.R.1
  • 10
    • 0000572133 scopus 로고
    • A new chemiluminescent system
    • Chandross, E. A., (1963) A new chemiluminescent system. Tetrahedron Lett. 4, 761-765.
    • (1963) Tetrahedron Lett. , vol.4 , pp. 761-765
    • Chandross, E.A.1
  • 11
    • 0002758648 scopus 로고
    • Chemiluminescence from concerted peroxide decomposition reactions
    • Rauhut, M. M., (1969) Chemiluminescence from concerted peroxide decomposition reactions. Acc. Chem. Res. 2, 80-87.
    • (1969) Acc. Chem. Res. , vol.2 , pp. 80-87
    • Rauhut, M.M.1
  • 12
    • 34247133913 scopus 로고    scopus 로고
    • Chemiluminescence of organic peroxides
    • (Edited by Z. Rappoport), Wiley & Sons, Chichester
    • Baader, W. J., C. V. Stevani, and, E. L. Bastos, (2006) Chemiluminescence of organic peroxides. In The Chemistry of Peroxides, Vol. 2 (Edited by, Z. Rappoport,), pp. 1211-1278. Wiley & Sons, Chichester.
    • (2006) The Chemistry of Peroxides , vol.2 , pp. 1211-1278
    • Baader, W.J.1    Stevani, C.V.2    Bastos, E.L.3
  • 13
    • 0001297145 scopus 로고
    • Luminescence in the thermal decomposition of 3,3,4-trimethyl-1,2- dioxetane
    • Kopecky, K. R., and, C. Mumford, (1969) Luminescence in the thermal decomposition of 3,3,4-trimethyl-1,2-dioxetane. Can. J. Chem. 47, 709-711.
    • (1969) Can. J. Chem. , vol.47 , pp. 709-711
    • Kopecky, K.R.1    Mumford, C.2
  • 14
    • 0343180664 scopus 로고
    • An α-peroxylactone. Synthesis and chemiluminescence
    • Adam, W., and, J.-C. Liu, (1972) An α-peroxylactone. Synthesis and chemiluminescence. J. Am. Chem. Soc. 94, 2894-2895.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 2894-2895
    • Adam, W.1    Liu, J.-C.2
  • 15
    • 0029826060 scopus 로고    scopus 로고
    • From the firefly bioluminescence to the dioxetane-based (AMPPD) chemiluminescence immunoassay: A retroanalysis
    • Adam, W., D. Reinhardt, and, C. R. Saha-Möller, (1996) From the firefly bioluminescence to the dioxetane-based (AMPPD) chemiluminescence immunoassay: A retroanalysis. Analyst 121, 1527-1531.
    • (1996) Analyst , vol.121 , pp. 1527-1531
    • Adam, W.1    Reinhardt, D.2    Saha-Möller, C.R.3
  • 16
    • 2442495183 scopus 로고    scopus 로고
    • Advanced chemistry of dioxetane-based chemiluminescent substrates originating from bioluminescence
    • Matsumoto, M., (2004) Advanced chemistry of dioxetane-based chemiluminescent substrates originating from bioluminescence. J. Photochem. Photobiol., C 5, 27-53.
    • (2004) J. Photochem. Photobiol., C , vol.5 , pp. 27-53
    • Matsumoto, M.1
  • 17
    • 37049141996 scopus 로고
    • An application of the theory of electrocyclic reactions to bioluminescence
    • McCapra, F., (1968) An application of the theory of electrocyclic reactions to bioluminescence. Chem. Commun. 155-156.
    • (1968) Chem. Commun. , pp. 155-156
    • McCapra, F.1
  • 18
    • 0000158035 scopus 로고
    • Four-membered-ring peroxides as excited states equivalents: A new dimension in bioorganic chemistry
    • Adam, W., and, G. Cilento, (1983) Four-membered-ring peroxides as excited states equivalents: A new dimension in bioorganic chemistry. Angew. Chem. Int. Ed. 22, 529-542.
    • (1983) Angew. Chem. Int. Ed. , vol.22 , pp. 529-542
    • Adam, W.1    Cilento, G.2
  • 19
    • 0001218439 scopus 로고
    • Dioxetanes and α-peroxy lactones, four-membered-ring cyclic peroxides
    • (Edited by W. Ando), Wiley, Chichester
    • Adam, W., M. Heil, T. Mosandl, and, C. R. Saha-Möller, (1992) Dioxetanes and α-peroxy lactones, four-membered-ring cyclic peroxides. In Organic Peroxides. (Edited by, W. Ando,), pp. 221-254. Wiley, Chichester.
    • (1992) Organic Peroxides , pp. 221-254
    • Adam, W.1    Heil, M.2    Mosandl, T.3    Saha-Möller, C.R.4
  • 21
    • 0001188173 scopus 로고
    • Thermal generation of electronic excitation with hyperenergetic molecules
    • Adam, W., (1980) Thermal generation of electronic excitation with hyperenergetic molecules. Pure Appl. Chem. 52, 2591-2608.
    • (1980) Pure Appl. Chem. , vol.52 , pp. 2591-2608
    • Adam, W.1
  • 22
    • 5644278452 scopus 로고
    • Chemiluminescence of organic peroxides. Conversion of ground-state reactants to excited state products by the chemically initiated electron-exchange luminescence mechanism
    • Schuster, G. B., (1979) Chemiluminescence of organic peroxides. Conversion of ground-state reactants to excited state products by the chemically initiated electron-exchange luminescence mechanism. Acc. Chem. Res. 12, 366-373.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 366-373
    • Schuster, G.B.1
  • 23
    • 84989718499 scopus 로고
    • Comments on the mechanisms of chemi- and bioluminescence
    • Wilson, T., (1995) Comments on the mechanisms of chemi- and bioluminescence. Photochem. Photobiol. 62, 601-606.
    • (1995) Photochem. Photobiol. , vol.62 , pp. 601-606
    • Wilson, T.1
  • 24
    • 0000224095 scopus 로고    scopus 로고
    • Quimiluminescência de Perõxidos Orgânicos: Geração de Estados Eletronicamente Excitados na Decomposição de 1,2-Dioxetanos
    • Nery, A. L. P., and, W. J. Baader, (2001) Quimiluminescência de Perõxidos Orgânicos: Geração de Estados Eletronicamente Excitados na Decomposição de 1,2-Dioxetanos. Quim. Nova 24, 626-636.
    • (2001) Quim. Nova , vol.24 , pp. 626-636
    • Nery, A.L.P.1    Baader, W.J.2
  • 25
    • 0000396699 scopus 로고
    • Chemiluminescence in the liquid phase: Thermal cleavage of dioxetanes
    • Wilson, T., (1976) Chemiluminescence in the liquid phase: Thermal cleavage of dioxetanes. Int. Rev. Sci. Phys. Chem. Ser. Two 9, 266-322.
    • (1976) Int. Rev. Sci. Phys. Chem. Ser. Two , vol.9 , pp. 266-322
    • Wilson, T.1
  • 26
    • 0010928512 scopus 로고
    • Chemiluminescence of organic-compounds
    • Schuster, G. B., and, S. P. Schmidt, (1982) Chemiluminescence of organic-compounds. Adv. Phys. Org. Chem. 18, 187-238.
    • (1982) Adv. Phys. Org. Chem. , vol.18 , pp. 187-238
    • Schuster, G.B.1    Schmidt, S.P.2
  • 27
    • 0021817764 scopus 로고
    • Effects of methylation on the thermal stability and chemiluminescence properties of 1,2-dioxetanes
    • Adam, W., and, W. J. Baader, (1985) Effects of methylation on the thermal stability and chemiluminescence properties of 1,2-dioxetanes. J. Am. Chem. Soc. 107, 410-416.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 410-416
    • Adam, W.1    Baader, W.J.2
  • 28
    • 0013270761 scopus 로고    scopus 로고
    • Mechanisms in chemiluminescence and bioluminescence - Unfinished business
    • (Edited by J. W. Hastings, L. J. Kricka and P. E. Stanley), Wiley & Sons: Chichester
    • McCapra, F., (1996) Mechanisms in chemiluminescence and bioluminescence-Unfinished business. In Bioluminescence and Chemiluminescence: Molecular Reporting with Photons. (Edited by, J. W. Hastings, L. J. Kricka, and, P. E. Stanley,), pp. 7-15. Wiley & Sons: Chichester.
    • (1996) Bioluminescence and Chemiluminescence: Molecular Reporting with Photons , pp. 7-15
    • McCapra, F.1
  • 29
    • 84855611259 scopus 로고
    • Thermal and photochemical generation of electronically excited organic molecules
    • Turro, N. J., and, P. Lechtken, (1973) Thermal and photochemical generation of electronically excited organic molecules. Pure Appl. Chem. 33, 363-388.
    • (1973) Pure Appl. Chem. , vol.33 , pp. 363-388
    • Turro, N.J.1    Lechtken, P.2
  • 30
    • 0001356667 scopus 로고
    • Thermochemistry of 1,2-dioxetane and its methylated derivatives. Estimation of activation parameters
    • O'Neal, H. E., and, W. H. Richardson, (1970) Thermochemistry of 1,2-dioxetane and its methylated derivatives. Estimation of activation parameters. J. Am. Chem. Soc. 92, 6553-6557.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 6553-6557
    • O'Neal, H.E.1    Richardson, W.H.2
  • 31
    • 0008758266 scopus 로고
    • Thermochemistry and estimated activation parameters for the thermal decomposition of 1,2-dioxetanedione, 4-tert-butyl-1,2-dioxetan-3-one and 4,4-dimethyl-1,2-dioxetan-3-one
    • Richardson, W. H., and, H. E. O'Neal, (1972) Thermochemistry and estimated activation parameters for the thermal decomposition of 1,2-dioxetanedione, 4-tert-butyl-1,2-dioxetan-3-one and 4,4-dimethyl-1,2- dioxetan-3-one. J. Am. Chem. Soc. 94, 8665-8668.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 8665-8668
    • Richardson, W.H.1    O'Neal, H.E.2
  • 32
    • 33746274399 scopus 로고
    • Excited-state energy distribution between dissimilar carbonyl molecules produced from 1,2-dioxetanes
    • Richardson, W. H., M. B. Lovett, M. E. Price, and, J. H. Anderegg, (1979) Excited-state energy distribution between dissimilar carbonyl molecules produced from 1,2-dioxetanes. J. Am. Chem. Soc. 101, 4683-4687.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 4683-4687
    • Richardson, W.H.1    Lovett, M.B.2    Price, M.E.3    Anderegg, J.H.4
  • 33
    • 0009952519 scopus 로고
    • Excited-state selectivity in the thermolysis of a 3,4-diaryl-3,4- dimethyl-1,2-dioxetane
    • Richardson, W. H., G. Batinica, K. Janotaperret, T. Miller, and, D. M. Shen, (1991) Excited-state selectivity in the thermolysis of a 3,4-diaryl-3,4-dimethyl-1,2-dioxetane. J. Org. Chem. 56, 6140-6144.
    • (1991) J. Org. Chem. , vol.56 , pp. 6140-6144
    • Richardson, W.H.1    Batinica, G.2    Janotaperret, K.3    Miller, T.4    Shen, D.M.5
  • 34
    • 84985482378 scopus 로고
    • Dioxetane decomposition revisited: A semi-empirical study of the potential energy surface
    • Wilson, T., and, A. M. Halpern, (1995) Dioxetane decomposition revisited: A semi-empirical study of the potential energy surface. J. Phys. Org. Chem. 8, 359-363.
    • (1995) J. Phys. Org. Chem. , vol.8 , pp. 359-363
    • Wilson, T.1    Halpern, A.M.2
  • 35
    • 33846461706 scopus 로고    scopus 로고
    • Theoretical studies on thermal stability of alkyl-substituted 1,2-dioxetanes
    • Bastos, E. L., and, W. J. Baader, (2007) Theoretical studies on thermal stability of alkyl-substituted 1,2-dioxetanes. Arkivoc 2007, 257-272.
    • (2007) Arkivoc , vol.2007 , pp. 257-272
    • Bastos, E.L.1    Baader, W.J.2
  • 36
    • 0001038787 scopus 로고
    • Chemiexcitation mechanisms - Role of symmetry and spin-orbit-coupling in diradicals
    • Turro, N. J., and, A. Devaquet, (1975) Chemiexcitation mechanisms-Role of symmetry and spin-orbit-coupling in diradicals. J. Am. Chem. Soc. 97, 3859-3862.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 3859-3862
    • Turro, N.J.1    Devaquet, A.2
  • 37
    • 84985609912 scopus 로고
    • 1,2-Dioxetane: Synthesis, characterization, stability and chemiluminescence
    • Adam, W., and, W. J. Baader, (1984) 1,2-Dioxetane: Synthesis, characterization, stability and chemiluminescence. Angew. Chem. Int. Ed. 23, 166-167.
    • (1984) Angew. Chem. Int. Ed. , vol.23 , pp. 166-167
    • Adam, W.1    Baader, W.J.2
  • 38
    • 0011146572 scopus 로고
    • The chemistry of 1,2-dioxetanes
    • Adam, W., (1977) The chemistry of 1,2-dioxetanes. Adv. Heterocycl. Chem. 21, 437-481.
    • (1977) Adv. Heterocycl. Chem. , vol.21 , pp. 437-481
    • Adam, W.1
  • 39
    • 33645968459 scopus 로고
    • Four-membered-ring peroxide heterocycles: Photochemistry through the Backdoor
    • Adam, W., W. J. Baader, C. Babatsikos, and, E. Schmidt, (1984) Four-membered-ring peroxide heterocycles: Photochemistry through the Backdoor. Bull. Soc. Chim. Belg. 93, 605-617.
    • (1984) Bull. Soc. Chim. Belg. , vol.93 , pp. 605-617
    • Adam, W.1    Baader, W.J.2    Babatsikos, C.3    Schmidt, E.4
  • 40
    • 0001377387 scopus 로고
    • Chemical and enzymatic triggering of 1,2-dioxetanes. 3: Alkaline phosphatase-catalyzed chemiluminescence from an aryl phosphate-substituted dioxetane
    • Schaap, A. P., M. D. Sandison, and, R. S. Handley, (1987) Chemical and enzymatic triggering of 1,2-dioxetanes. 3: Alkaline phosphatase-catalyzed chemiluminescence from an aryl phosphate-substituted dioxetane. Tetrahedron Lett. 28, 1159-1162.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 1159-1162
    • Schaap, A.P.1    Sandison, M.D.2    Handley, R.S.3
  • 41
  • 42
    • 0025081418 scopus 로고
    • Applications of dioxetane chemiluminescent probes to molecular biology
    • Beck, S., and, H. Köster, (1990) Applications of dioxetane chemiluminescent probes to molecular biology. Anal. Chem. 62, 2258-2270.
    • (1990) Anal. Chem. , vol.62 , pp. 2258-2270
    • Beck, S.1    Köster, H.2
  • 43
    • 0033119589 scopus 로고    scopus 로고
    • Automated detection of anti-double-stranded DNA antibody in systemic lupus erythematosus serum by flow immunoassay
    • Lim, T.-K., Y. Komoda, N. Nakamura, and, T. Matsunaga, (1999) Automated detection of anti-double-stranded DNA antibody in systemic lupus erythematosus serum by flow immunoassay. Anal. Chem. 71, 1298-1302.
    • (1999) Anal. Chem. , vol.71 , pp. 1298-1302
    • Lim, T.-K.1    Komoda, Y.2    Nakamura, N.3    Matsunaga, T.4
  • 44
    • 3042523648 scopus 로고
    • Chemiluminescent thermolysis of α-peroxylactones
    • Turro, N. J., and, M.-F. Chow, (1980) Chemiluminescent thermolysis of α-peroxylactones. J. Am. Chem. Soc. 102, 5058-5064.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5058-5064
    • Turro, N.J.1    Chow, M.-F.2
  • 45
    • 49049109519 scopus 로고    scopus 로고
    • Electrogenerated chemiluminescence and its biorelated applications
    • Miao, W., (2008) Electrogenerated chemiluminescence and its biorelated applications. Chem. Rev. 108, 2506-2553.
    • (2008) Chem. Rev. , vol.108 , pp. 2506-2553
    • Miao, W.1
  • 46
    • 0002288455 scopus 로고
    • Eletrochemiluminescence at a silicon anode in contact with an electrolyte
    • Gee, A., (1960) Eletrochemiluminescence at a silicon anode in contact with an electrolyte. J. Eletrochem. Soc. 107, 787-788.
    • (1960) J. Eletrochem. Soc. , vol.107 , pp. 787-788
    • Gee, A.1
  • 47
    • 0001556630 scopus 로고
    • Chemiluminescence resulting from eletrochemically generated species
    • Hercules, D. M., (1964) Chemiluminescence resulting from eletrochemically generated species. Science 145, 808-809.
    • (1964) Science , vol.145 , pp. 808-809
    • Hercules, D.M.1
  • 48
    • 0011141640 scopus 로고
    • Electroluminescence in solutions of aromatic hydrocarbons
    • Visco, R. E., and, E. A. Chandross, (1964) Electroluminescence in solutions of aromatic hydrocarbons. J. Am. Chem. Soc. 86, 5350-5351.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 5350-5351
    • Visco, R.E.1    Chandross, E.A.2
  • 49
    • 0000522710 scopus 로고
    • Chemiluminescence of electrogenerated 9,10-diphenylanthracene anion radical
    • Santhanam, K. S., and, A. J. Bard, (1965) Chemiluminescence of electrogenerated 9,10-diphenylanthracene anion radical. J. Am. Chem. Soc. 87, 139-140.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 139-140
    • Santhanam, K.S.1    Bard, A.J.2
  • 50
    • 33947092674 scopus 로고
    • Chemiluminescence of diphenoyl peroxide. Chemically initiated electron exchange luminescence. A new general mechanism for chemical production of electronically excited states
    • Koo, J.-Y., and, G. B. Schuster, (1978) Chemiluminescence of diphenoyl peroxide. Chemically initiated electron exchange luminescence. A new general mechanism for chemical production of electronically excited states. J. Am. Chem. Soc. 100, 4496-4503.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 4496-4503
    • Koo, J.-Y.1    Schuster, G.B.2
  • 51
    • 0004197749 scopus 로고
    • Eletrochemiluminescence
    • (Edited by W. Adam and G. Cilento), Academic Press, New York
    • Faulkner, L. R., and, R. S. Glass, (1982) Eletrochemiluminescence. In Chemical and Biological Generation of Excited States. (Edited by, W. Adam, and, G. Cilento,), pp. 191-227. Academic Press, New York.
    • (1982) Chemical and Biological Generation of Excited States , pp. 191-227
    • Faulkner, L.R.1    Glass, R.S.2
  • 54
    • 0000727348 scopus 로고
    • Chemiluminescence of dimethyldioxetanone - Unimolecular generation of excited singlet and triplet acetone. Chemically initiated electron-exchange luminescence, the primary light generating reaction
    • Schmidt, S. P., and, G. B. Schuster, (1980) Chemiluminescence of dimethyldioxetanone-Unimolecular generation of excited singlet and triplet acetone. Chemically initiated electron-exchange luminescence, the primary light generating reaction. J. Am. Chem. Soc. 102, 306-314.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 306-314
    • Schmidt, S.P.1    Schuster, G.B.2
  • 55
    • 0006317121 scopus 로고
    • Dioxetanone chemiluminescence by the chemically initiated electron exchange pathway. Efficient generation of excited singlet states
    • Schmidt, S. P., and, G. B. Schuster, (1978) Dioxetanone chemiluminescence by the chemically initiated electron exchange pathway. Efficient generation of excited singlet states. J. Am. Chem. Soc. 100, 1966-1968.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 1966-1968
    • Schmidt, S.P.1    Schuster, G.B.2
  • 56
    • 20944434701 scopus 로고
    • Mechanism of direct and rubrene enhanced chemiluminescence during α-peroxylactone decarboxylation
    • Adam, W., G. A. Simpson, and, F. Yany, (1974) Mechanism of direct and rubrene enhanced chemiluminescence during α-peroxylactone decarboxylation. J. Phys. Chem. 78, 2559-2569.
    • (1974) J. Phys. Chem. , vol.78 , pp. 2559-2569
    • Adam, W.1    Simpson, G.A.2    Yany, F.3
  • 57
    • 0000888480 scopus 로고
    • Fluorescer-enhanced chemiluminescence of α-peroxylactones via electron exchange
    • Adam, W., and, O. Cueto, (1979) Fluorescer-enhanced chemiluminescence of α-peroxylactones via electron exchange. J. Am. Chem. Soc. 101, 6511-6515.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 6511-6515
    • Adam, W.1    Cueto, O.2
  • 58
    • 0000087592 scopus 로고
    • Electron transfer and chemiluminescence. Two inefficient systems: 1,4-dimethoxy-9,10-diphenylanthracene peroxide and diphenoyl peroxide
    • Catalani, L. H., and, T. Wilson, (1989) Electron transfer and chemiluminescence. Two inefficient systems: 1,4-dimethoxy-9,10- diphenylanthracene peroxide and diphenoyl peroxide. J. Am. Chem. Soc. 111, 2633-2639.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2633-2639
    • Catalani, L.H.1    Wilson, T.2
  • 59
    • 0034525457 scopus 로고    scopus 로고
    • Studies on the mechanism of the excitation step in peroxyoxalate system
    • Stevani, C. V., S. M. Silva, and, W. J. Baader, (2000) Studies on the mechanism of the excitation step in peroxyoxalate system. Eur. J. Org. Chem. 4037-4046.
    • (2000) Eur. J. Org. Chem. , pp. 4037-4046
    • Stevani, C.V.1    Silva, S.M.2    Baader, W.J.3
  • 60
    • 0024698415 scopus 로고
    • Determination of absolute chemiluminescence quantum yields for reactions of bis-(pentachlorophenyl) oxalate, hydrogen peroxide and fluorescent compounds
    • Catherall, C. L. R., T. F. Palmer, and, R. B. Cundall, (1989) Determination of absolute chemiluminescence quantum yields for reactions of bis-(pentachlorophenyl) oxalate, hydrogen peroxide and fluorescent compounds. J. Biolumin. Chemilumin. 3, 147-154.
    • (1989) J. Biolumin. Chemilumin. , vol.3 , pp. 147-154
    • Catherall, C.L.R.1    Palmer, T.F.2    Cundall, R.B.3
  • 61
    • 84869498685 scopus 로고    scopus 로고
    • Chemiluminescence characteristics of furan derivatives as blue fluorescers in peroxyoxalate-hydrogen peroxide system
    • Chaichi, M. J., S. N. Azizi, M. Heidarpour, O. Aalijanpour, and, M. Qandalee, (2012) Chemiluminescence characteristics of furan derivatives as blue fluorescers in peroxyoxalate-hydrogen peroxide system. J. Fluoresc. 22, 1209-1216.
    • (2012) J. Fluoresc. , vol.22 , pp. 1209-1216
    • Chaichi, M.J.1    Azizi, S.N.2    Heidarpour, M.3    Aalijanpour, O.4    Qandalee, M.5
  • 62
    • 0000049615 scopus 로고    scopus 로고
    • A kinetic study on the peroxyoxalate reaction: Imidazole as nucleophilic catalyst
    • Stevani, C. V., D. F. Lima, V. G. Toscano, and, W. J. Baader, (1996) A kinetic study on the peroxyoxalate reaction: Imidazole as nucleophilic catalyst. J. Chem. Soc. Perkin Trans. 2, 989-995.
    • (1996) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 989-995
    • Stevani, C.V.1    Lima, D.F.2    Toscano, V.G.3    Baader, W.J.4
  • 63
    • 0036725899 scopus 로고    scopus 로고
    • Kinetic studies on the peroxyoxalate chemiluminescence reaction: Determination of the cyclization rate constant
    • Silva, S. M., F. Casallanovo Jr, K. H. Oyamaguchi, L. F. M. L. Ciscato, C. V. Stevani, and, W. J. Baader, (2002) Kinetic studies on the peroxyoxalate chemiluminescence reaction: Determination of the cyclization rate constant. Luminescence 17, 313-320.
    • (2002) Luminescence , vol.17 , pp. 313-320
    • Silva, S.M.1    Casallanovo Jr., F.2    Oyamaguchi, K.H.3    Ciscato, L.F.M.L.4    Stevani, C.V.5    Baader, W.J.6
  • 65
    • 41949106876 scopus 로고    scopus 로고
    • Studies on the mechanism of peroxyoxalate chemiluminescence reaction. Part 2: Further identification of intermediates using 2D EXSY 13C nuclear magnetic resonance spectroscopy
    • Tonkin, S. A., R. Bos, G. A. Dyson, K. F. Lim, R. A. Russel, S. P. Watson, C. M. Hindson, and, N. W. Barnett, (2008) Studies on the mechanism of peroxyoxalate chemiluminescence reaction. Part 2: Further identification of intermediates using 2D EXSY 13C nuclear magnetic resonance spectroscopy. Anal. Chim. Acta 614, 173-181.
    • (2008) Anal. Chim. Acta , vol.614 , pp. 173-181
    • Tonkin, S.A.1    Bos, R.2    Dyson, G.A.3    Lim, K.F.4    Russel, R.A.5    Watson, S.P.6    Hindson, C.M.7    Barnett, N.W.8
  • 66
    • 0347063984 scopus 로고    scopus 로고
    • Studies on the mechanism of peroxyoxalate chemiluminescence reaction. Part 1: Confirmation of 1,2-dioxetanedione as an intermediate using 13C nuclear magnetic resonance spectroscopy
    • Bos, R., N. W. Barnett, G. A. Dyson, K. F. Lim, R. A. Russel, and, S. P. Watson, (2004) Studies on the mechanism of peroxyoxalate chemiluminescence reaction. Part 1: Confirmation of 1,2-dioxetanedione as an intermediate using 13C nuclear magnetic resonance spectroscopy. Anal. Chim. Acta 502, 141-147.
    • (2004) Anal. Chim. Acta , vol.502 , pp. 141-147
    • Bos, R.1    Barnett, N.W.2    Dyson, G.A.3    Lim, K.F.4    Russel, R.A.5    Watson, S.P.6
  • 67
    • 0042387908 scopus 로고    scopus 로고
    • Studies on the chemiexcitation step in peroxyoxalate chemiluminescence using steroid-substituted activators
    • Silva, S. M., K. Wagner, D. Weiss, R. Beckert, C. V. Stevani, and, W. J. Baader, (2002) Studies on the chemiexcitation step in peroxyoxalate chemiluminescence using steroid-substituted activators. Luminescence 17, 362-369.
    • (2002) Luminescence , vol.17 , pp. 362-369
    • Silva, S.M.1    Wagner, K.2    Weiss, D.3    Beckert, R.4    Stevani, C.V.5    Baader, W.J.6
  • 68
    • 72249115780 scopus 로고    scopus 로고
    • Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence
    • Ciscato, L. F. M. L., F. H. Bartoloni, E. L. Bastos, and, W. J. Baader, (2009) Direct kinetic observation of the chemiexcitation step in peroxyoxalate chemiluminescence. J. Org. Chem. 74, 8974-8979.
    • (2009) J. Org. Chem. , vol.74 , pp. 8974-8979
    • Ciscato, L.F.M.L.1    Bartoloni, F.H.2    Bastos, E.L.3    Baader, W.J.4
  • 70
    • 0001566958 scopus 로고
    • Chemiluminescence from a phenoxide-substituted 1,2-dioxetane: A model for firefly bioluminescence
    • Schaap, A. P., and, S. D. Gagnon, (1982) Chemiluminescence from a phenoxide-substituted 1,2-dioxetane: A model for firefly bioluminescence. J. Am. Chem. Soc. 104, 3504-3506.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 3504-3506
    • Schaap, A.P.1    Gagnon, S.D.2
  • 71
    • 0033605824 scopus 로고    scopus 로고
    • Fluoride-triggered decomposition of m-silyloxyphenyl-substituted 1,2-dioxetanes by an intramolecular electron transfer (CIEEL) mechanism
    • Nery, A. L. P., S. Röpke, L. H. Catalani, and, W. J. Baader, (1999) Fluoride-triggered decomposition of m-silyloxyphenyl-substituted 1,2-dioxetanes by an intramolecular electron transfer (CIEEL) mechanism. Tetrahedron Lett. 40, 2443-2446.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2443-2446
    • Nery, A.L.P.1    Röpke, S.2    Catalani, L.H.3    Baader, W.J.4
  • 72
    • 0342646982 scopus 로고    scopus 로고
    • Studies on the intramolecular electron transfer catalyzed thermolysis of 1,2-dioxetanes
    • Nery, A. L. P., D. Weiss, L. H. Catalani, and, W. J. Baader, (2000) Studies on the intramolecular electron transfer catalyzed thermolysis of 1,2-dioxetanes. Tetrahedron 56, 5317-5327.
    • (2000) Tetrahedron , vol.56 , pp. 5317-5327
    • Nery, A.L.P.1    Weiss, D.2    Catalani, L.H.3    Baader, W.J.4
  • 73
    • 0000208084 scopus 로고
    • Enamine-singlet oxygen reactions. α-Diketones from intermediate amino dioxetanes
    • Wasserman, H. H., and, S. Terao, (1975) Enamine-singlet oxygen reactions. α-Diketones from intermediate amino dioxetanes. Tetrahedron Lett. 16, 1735-1738.
    • (1975) Tetrahedron Lett. , vol.16 , pp. 1735-1738
    • Wasserman, H.H.1    Terao, S.2
  • 74
    • 0002427410 scopus 로고
    • Chemistry of singlet oxygen. XX. Mechanism of the sensitized photooxidation of enamines
    • Foote, C. S., A. A. Dzakpasu, and, J. W.-P. Lin, (1975) Chemistry of singlet oxygen. XX. Mechanism of the sensitized photooxidation of enamines. Tetrahedron Lett. 16, 1247-1250.
    • (1975) Tetrahedron Lett. , vol.16 , pp. 1247-1250
    • Foote, C.S.1    Dzakpasu, A.A.2    Lin, J.W.-P.3
  • 75
    • 0343416488 scopus 로고
    • Singlet oxygen reaction. IV. Photooxygenation of enamines involving a two-step cleavage of a 1,2-dioxetane intermediate
    • Ando, W., T. Saiki, and, T. Migita, (1975) Singlet oxygen reaction. IV. Photooxygenation of enamines involving a two-step cleavage of a 1,2-dioxetane intermediate. J. Am. Chem. Soc. 97, 5028-5029.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5028-5029
    • Ando, W.1    Saiki, T.2    Migita, T.3
  • 76
    • 37049100269 scopus 로고
    • Aminodioxetanes. Preparation of the stable 3,3-dimethyl-4-[N-(2-methyl-1- hydroxypropyl)anthryl-amino]-1,2-dioxetane
    • Akutagawa, M., H. Aoyama, Y. Omote, and, H. Yamamoto, (1976) Aminodioxetanes. Preparation of the stable 3,3-dimethyl-4-[N-(2-methyl-1- hydroxypropyl)anthryl-amino]-1,2-dioxetane. J. Chem. Soc., Chem. Commun. 180-181.
    • (1976) J. Chem. Soc., Chem. Commun. , pp. 180-181
    • Akutagawa, M.1    Aoyama, H.2    Omote, Y.3    Yamamoto, H.4
  • 77
    • 49549139730 scopus 로고
    • Singlet oxygen reaction V. Ring size effects on the decomposition of sulfur substituted 1,2-dioxetane
    • Ando, W., K. Watanabe, and, T. Migita, (1975) Singlet oxygen reaction V. Ring size effects on the decomposition of sulfur substituted 1,2-dioxetane. Tetrahedron Lett. 16, 4127-4130.
    • (1975) Tetrahedron Lett. , vol.16 , pp. 4127-4130
    • Ando, W.1    Watanabe, K.2    Migita, T.3
  • 78
    • 0346986117 scopus 로고
    • Spiroadamantyl stabilization of sulfur-substituted 1,2-dioxetanes
    • Adam, W., L. A. Arias, and, D. Scheutzow, (1982) Spiroadamantyl stabilization of sulfur-substituted 1,2-dioxetanes. Tetrahedron Lett. 23, 2835-2836.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 2835-2836
    • Adam, W.1    Arias, L.A.2    Scheutzow, D.3
  • 79
    • 34548266203 scopus 로고
    • Chemistry of singlet oxygen. 41 Direct observation of a dioxetane from the singlet oxygen photooxygenation of a thioketene acetal
    • Geller, G. G., C. S. Foote, and, D. B. Pechman, (1983) Chemistry of singlet oxygen. 41 Direct observation of a dioxetane from the singlet oxygen photooxygenation of a thioketene acetal. Tetrahedron Lett. 24, 673-676.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 673-676
    • Geller, G.G.1    Foote, C.S.2    Pechman, D.B.3
  • 80
    • 0005757742 scopus 로고
    • Chemiluminescence from the reaction of singlet oxygen with 10,10′-dimethyl-9,9′-biacridylidene. A reactive 1,2-dioxetane
    • Lee, K.-W., L. A. Singer, and, K. D. Legg, (1976) Chemiluminescence from the reaction of singlet oxygen with 10,10′-dimethyl-9,9′- biacridylidene. A reactive 1,2-dioxetane. J. Org. Chem. 41, 2685-2688.
    • (1976) J. Org. Chem. , vol.41 , pp. 2685-2688
    • Lee, K.-W.1    Singer, L.A.2    Legg, K.D.3
  • 82
    • 0003502150 scopus 로고
    • 3,3,7,7-Bis-(10′-methyl-9′,9′-acridanyl)-1,2,5, 6-tetraoxocane, a dioxetane dimer, from the reaction of 10-methyl-9-methylene-9, 10-acridane with singlet oxygen
    • White, E. H., N. Suzuki, and, W. H. Hendrickson, (1979) 3,3,7,7-Bis-(10′-methyl-9′,9′-acridanyl)-1,2,5,6-tetraoxocane, a dioxetane dimer, from the reaction of 10-methyl-9-methylene-9,10-acridane with singlet oxygen. Chem. Lett. 8, 1491-1494.
    • (1979) Chem. Lett. , vol.8 , pp. 1491-1494
    • White, E.H.1    Suzuki, N.2    Hendrickson, W.H.3
  • 83
    • 33846213953 scopus 로고
    • 2-(1-Methylindol-3-yl)-3-phenyldihydro-1,4-dioxin-2,3-epidioxide, a Dioxetane Resulting in Efficient Ultraviolet Chemilumines-cence
    • Goto, T., and, H. Nakamura, (1978) 2-(1-Methylindol-3-yl)-3- phenyldihydro-1,4-dioxin-2,3-epidioxide, a Dioxetane Resulting in Efficient Ultraviolet Chemilumines-cence. J. Chem. Soc., Chem. Commun. 781-782.
    • (1978) J. Chem. Soc., Chem. Commun. , pp. 781-782
    • Goto, T.1    Nakamura, H.2
  • 84
    • 0000703894 scopus 로고
    • 1,2-Dioxetane formation in an indole system
    • Saito, I., S. Matsugo, and, T. Matsuura, (1979) 1,2-Dioxetane formation in an indole system. J. Am. Chem. Soc. 101, 4757-4759.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 4757-4759
    • Saito, I.1    Matsugo, S.2    Matsuura, T.3
  • 85
    • 37049091089 scopus 로고
    • Alternative mechanism for dioxetane decomposition
    • McCapra, F., (1977) Alternative mechanism for dioxetane decomposition. J. Chem. Soc., Chem. Commun. 946-948.
    • (1977) J. Chem. Soc., Chem. Commun. , pp. 946-948
    • McCapra, F.1
  • 86
    • 0002313888 scopus 로고
    • Bioluminescence of the firefly: Key steps in the formation of the electronically excited state for model systems
    • Koo, J.-Y., S. P. Schmidt, and, G. B. Schuster, (1978) Bioluminescence of the firefly: Key steps in the formation of the electronically excited state for model systems. Proc. Natl Acad. Sci. USA 75, 30-33.
    • (1978) Proc. Natl Acad. Sci. USA , vol.75 , pp. 30-33
    • Koo, J.-Y.1    Schmidt, S.P.2    Schuster, G.B.3
  • 87
    • 0000465158 scopus 로고
    • Chemical and enzimatic triggering of 1,2-dioxetanes. 1: Aryl esterase-catalyzed chemiluminescence from a naphthyl acetate-substitute dioxetane
    • Schaap, A. P., R. S. Handley, and, B. P. Giri, (1987) Chemical and enzimatic triggering of 1,2-dioxetanes. 1: Aryl esterase-catalyzed chemiluminescence from a naphthyl acetate-substitute dioxetane. Tetrahedron Lett. 28, 935-938.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 935-938
    • Schaap, A.P.1    Handley, R.S.2    Giri, B.P.3
  • 88
    • 0001543853 scopus 로고
    • Chemical and enzimatic triggering of 1,2-dioxetanes. 2: Fluoride-induced chemiluminescence from tert-butyldimethylsilyloxy-substituted dioxetanes
    • Schaap, A. P., T.-S. Chen, R. S. Handley, R. DeSilva, and, B. P. Giri, (1987) Chemical and enzimatic triggering of 1,2-dioxetanes. 2: Fluoride-induced chemiluminescence from tert-butyldimethylsilyloxy-substituted dioxetanes. Tetrahedron Lett. 28, 1155-1158.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 1155-1158
    • Schaap, A.P.1    Chen, T.-S.2    Handley, R.S.3    Desilva, R.4    Giri, B.P.5
  • 89
    • 77957150257 scopus 로고    scopus 로고
    • Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition
    • Ciscato, L. F. M. L., F. H. Bartoloni, D. Weiss, R. Beckert, and, W. J. Baader, (2010) Experimental evidence of the occurrence of intramolecular electron transfer in catalyzed 1,2-dioxetane decomposition. J. Org. Chem. 75, 6574-6580.
    • (2010) J. Org. Chem. , vol.75 , pp. 6574-6580
    • Ciscato, L.F.M.L.1    Bartoloni, F.H.2    Weiss, D.3    Beckert, R.4    Baader, W.J.5
  • 91
    • 84877149769 scopus 로고    scopus 로고
    • Solvent cage effects: Basis of a general mechanism for efficient chemiluminescence
    • Bastos, E. L., S. M. Silva, and, W. J. Baader, (2013) Solvent cage effects: Basis of a general mechanism for efficient chemiluminescence. J. Org. Chem. 78, 4432-4439.
    • (2013) J. Org. Chem. , vol.78 , pp. 4432-4439
    • Bastos, E.L.1    Silva, S.M.2    Baader, W.J.3
  • 92
    • 0342906383 scopus 로고
    • Determination of chemiexcitation yields in the thermal generation of electronic excitation from 1,2-dioxetanes
    • (Edited by W. Adam and G. Cilento), Academic Press, New York
    • Adam, W., (1982) Determination of chemiexcitation yields in the thermal generation of electronic excitation from 1,2-dioxetanes. In Chemical and Biological Generation of Excited States. (Edited by, W. Adam, and, G. Cilento,), pp. 115-152. Academic Press, New York.
    • (1982) Chemical and Biological Generation of Excited States , pp. 115-152
    • Adam, W.1
  • 93
    • 0001762872 scopus 로고
    • Total quantum flux of isotropic sources
    • Hastings, J. W., and, G. J. Weber, (1963) Total quantum flux of isotropic sources. J. Opt. Soc. Am. 53, 1410-1415.
    • (1963) J. Opt. Soc. Am. , vol.53 , pp. 1410-1415
    • Hastings, J.W.1    Weber, G.J.2
  • 94
    • 0013820777 scopus 로고
    • Absolute spectral sensitivity of phototubes and the application to the measurement of the absolute quantum yields of chemilumines-cence and bioluminescence
    • Lee, J., and, H. H. Seliger, (1965) Absolute spectral sensitivity of phototubes and the application to the measurement of the absolute quantum yields of chemilumines-cence and bioluminescence. Photochem. Photobiol. 4, 1015-1048.
    • (1965) Photochem. Photobiol. , vol.4 , pp. 1015-1048
    • Lee, J.1    Seliger, H.H.2
  • 95
    • 0001611760 scopus 로고    scopus 로고
    • Chemically initiated electron exchange luminescence of silyloxyaryl-substituted spiroadamantyl dioxetanes: Kinetics and excited state yields
    • Trofimov, A. V., K. Mielke, R. F. Vasil'ev, and, W. Adam, (1996) Chemically initiated electron exchange luminescence of silyloxyaryl-substituted spiroadamantyl dioxetanes: Kinetics and excited state yields. Photochem. Photobiol. 63, 463-467.
    • (1996) Photochem. Photobiol. , vol.63 , pp. 463-467
    • Trofimov, A.V.1    Mielke, K.2    Vasil'Ev, R.F.3    Adam, W.4
  • 97
    • 0004082709 scopus 로고    scopus 로고
    • Contemporary trends in dioxetane chemistry
    • (Edited by Z. Rappoport), Wiley & Sons, Chichester
    • Adam, W., and, A. V. Trofimov, (2006) Contemporary trends in dioxetane chemistry. In The Chemistry of Peroxides, Vol 2 (Edited by, Z. Rappoport,), pp. 1171-1209. Wiley & Sons, Chichester.
    • (2006) The Chemistry of Peroxides , vol.2 , pp. 1171-1209
    • Adam, W.1    Trofimov, A.V.2
  • 98
    • 33845551427 scopus 로고
    • Thermolysis of 4-methyl-4-phenylmalonyl peroxide: A new oxygen dependent chemiluminescent reaction
    • Porter, J. E., and, G. B. Schuster, (1983) Thermolysis of 4-methyl-4-phenylmalonyl peroxide: A new oxygen dependent chemiluminescent reaction. J. Org. Chem. 48, 4944-4947.
    • (1983) J. Org. Chem. , vol.48 , pp. 4944-4947
    • Porter, J.E.1    Schuster, G.B.2
  • 99
    • 0001517734 scopus 로고
    • Chemiluminescence of secondary peroxyesters
    • Dixon, B. G., and, G. B. Schuster, (1981) Chemiluminescence of secondary peroxyesters. J. Am. Chem. Soc. 103, 3068-3077.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3068-3077
    • Dixon, B.G.1    Schuster, G.B.2
  • 100
    • 0000294904 scopus 로고
    • Structural effects on the intramolecular electron transfer induced decomposition of a series of 1,2-dioxetanes derived from 9-alkylidene-10- methylacridans
    • Lee, C., and, L. A. Singer, (1980) Structural effects on the intramolecular electron transfer induced decomposition of a series of 1,2-dioxetanes derived from 9-alkylidene-10-methylacridans. J. Am. Chem. Soc. 102, 3823-3829.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 3823-3829
    • Lee, C.1    Singer, L.A.2
  • 101
    • 0002124129 scopus 로고
    • Photochemical (2+2) cycloaddition of and thermal decomposition to N-methylacridone and acetone: Chemiluminescence as a probe of possible formation of 1,2-dioxetanes
    • Suzuki, N., Y. Kazui, and, Y. Izawa, (1982) Photochemical (2+2) cycloaddition of and thermal decomposition to N-methylacridone and acetone: Chemiluminescence as a probe of possible formation of 1,2-dioxetanes. Tetrahedron Lett. 23, 95-96.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 95-96
    • Suzuki, N.1    Kazui, Y.2    Izawa, Y.3
  • 102
    • 0038639785 scopus 로고    scopus 로고
    • Reversible formation of excited states in intramolecular donor assisted chemiluminescence reactions of dioxetanes
    • Singh, S., and, E. F. Ullman, (2003) Reversible formation of excited states in intramolecular donor assisted chemiluminescence reactions of dioxetanes. Chem. Commun. 1756-1757.
    • (2003) Chem. Commun. , pp. 1756-1757
    • Singh, S.1    Ullman, E.F.2
  • 103
    • 22244481260 scopus 로고    scopus 로고
    • New triggering system for dioxetane-based chemiluminescence: Base-induced decomposition of bicyclic dioxetanes bearing a 3-aminophenyl or 2-phenylindol-6-yl moiety
    • Watanabe, N., M. Ichikawa, A. Ono, H. Murakami, and, M. Matsumoto, (2005) New triggering system for dioxetane-based chemiluminescence: Base-induced decomposition of bicyclic dioxetanes bearing a 3-aminophenyl or 2-phenylindol-6-yl moiety. Chem. Lett. 34, 718-719.
    • (2005) Chem. Lett. , vol.34 , pp. 718-719
    • Watanabe, N.1    Ichikawa, M.2    Ono, A.3    Murakami, H.4    Matsumoto, M.5
  • 104
    • 75749094371 scopus 로고    scopus 로고
    • Synthesis of sulfanyl-, sulfinyl-, and sulfonyl-substituted bicyclic dioxetanes and their base-induced chemiluminescence
    • Watanabe, N., M. Kikuchi, Y. Maniwa, H. K. Ijuin, and, M. Matsumoto, (2010) Synthesis of sulfanyl-, sulfinyl-, and sulfonyl-substituted bicyclic dioxetanes and their base-induced chemiluminescence. J. Org. Chem. 75, 879-884.
    • (2010) J. Org. Chem. , vol.75 , pp. 879-884
    • Watanabe, N.1    Kikuchi, M.2    Maniwa, Y.3    Ijuin, H.K.4    Matsumoto, M.5
  • 105
    • 48149113094 scopus 로고    scopus 로고
    • Rotamer-dependent chemiluminescence in the intramolecular charge-transfer-induced decomposition of bicyclic dioxetanes bearing a hydroxyaryl group
    • Matsumoto, M., H. Suzuki, Y. Sano, N. Watanabe, and, H. K. Ijuin, (2008) Rotamer-dependent chemiluminescence in the intramolecular charge-transfer- induced decomposition of bicyclic dioxetanes bearing a hydroxyaryl group. Tetrahedron Lett. 49, 5372-5375.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 5372-5375
    • Matsumoto, M.1    Suzuki, H.2    Sano, Y.3    Watanabe, N.4    Ijuin, H.K.5
  • 106
    • 77956141589 scopus 로고    scopus 로고
    • Synthesis of thermally stable acylamino-substituted bicyclic dioxetanes and their base-induced chemiluminescent decomposition
    • Watanabe, N., Y. Sano, H. Suzuki, M. Tanimura, H. K. Ijuin, and, M. Matsumoto, (2010) Synthesis of thermally stable acylamino-substituted bicyclic dioxetanes and their base-induced chemiluminescent decomposition. J. Org. Chem. 75, 5920-5926.
    • (2010) J. Org. Chem. , vol.75 , pp. 5920-5926
    • Watanabe, N.1    Sano, Y.2    Suzuki, H.3    Tanimura, M.4    Ijuin, H.K.5    Matsumoto, M.6
  • 107
    • 79958816191 scopus 로고    scopus 로고
    • Crucial dependence of chemiluminescence efficiency on the syn/anti conformation for intramolecular charge-transfer induced decomposition of bicyclic dioxetanes bearing an oxidoaryl group
    • Matsumoto, M., H. Suzuki, N. Watanabe, H. K. Ijuin, J. Tanaka, and, C. Tanaka, (2011) Crucial dependence of chemiluminescence efficiency on the syn/anti conformation for intramolecular charge-transfer induced decomposition of bicyclic dioxetanes bearing an oxidoaryl group. J. Org. Chem. 76, 5006-5017.
    • (2011) J. Org. Chem. , vol.76 , pp. 5006-5017
    • Matsumoto, M.1    Suzuki, H.2    Watanabe, N.3    Ijuin, H.K.4    Tanaka, J.5    Tanaka, C.6
  • 108
    • 0035842131 scopus 로고    scopus 로고
    • Base-induced chemiluminescence of 5-tert-butyl-1-(4-hydroxybenz[d]oxazol- 6-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptanes: Chemiluminescence- chemiexcitation profile in aqueous medium
    • Matsumoto, M., Y. Mizoguchi, T. Motoyama, and, N. Watanabe, (2001) Base-induced chemiluminescence of 5-tert-butyl-1-(4-hydroxybenz[d]oxazol-6-yl)- 4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptanes: Chemiluminescence- chemiexcitation profile in aqueous medium. Tetrahedron Lett. 42, 8869-8872.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 8869-8872
    • Matsumoto, M.1    Mizoguchi, Y.2    Motoyama, T.3    Watanabe, N.4
  • 109
    • 4644370965 scopus 로고    scopus 로고
    • Color modulation for chemiluminescence of a dioxetane bearing a 3-(antracen-9-yl)-5-hydroxyphenyl moiety induced by a complex of crown ether with potassium tert-butoxide
    • Matsumoto, M., D. Kasai, K. Yamada, N. Fukuda, N. Watanabe, and, H. K. Ijuin, (2004) Color modulation for chemiluminescence of a dioxetane bearing a 3-(antracen-9-yl)-5-hydroxyphenyl moiety induced by a complex of crown ether with potassium tert-butoxide. Tetrahedron Lett. 45, 8079-8082.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 8079-8082
    • Matsumoto, M.1    Kasai, D.2    Yamada, K.3    Fukuda, N.4    Watanabe, N.5    Ijuin, H.K.6
  • 110
    • 33646384131 scopus 로고    scopus 로고
    • Synthesis and fluoride-induced chemiluminescent decomposition of bicyclic dioxetanes substituted with a 2-hydroxynaphthyl group
    • Hoshiya, N., N. Fukuda, H. Maeda, N. Watanabe, and, M. Matsumoto, (2006) Synthesis and fluoride-induced chemiluminescent decomposition of bicyclic dioxetanes substituted with a 2-hydroxynaphthyl group. Tetrahedron 62, 5808-5820.
    • (2006) Tetrahedron , vol.62 , pp. 5808-5820
    • Hoshiya, N.1    Fukuda, N.2    Maeda, H.3    Watanabe, N.4    Matsumoto, M.5
  • 111
    • 0034343755 scopus 로고    scopus 로고
    • Back electron transfer in electron-exchange chemiluminescence of oxyaryl-substituted spiro-adamantyl dioxetane, an analog of firefly bioluminescence
    • Adam, W., I. Bronstein, R. F. Vasil'ev, and, A. V. Trofimov, (2000) Back electron transfer in electron-exchange chemiluminescence of oxyaryl-substituted spiro-adamantyl dioxetane, an analog of firefly bioluminescence. Russ. Chem. Bull. 49, 659-665.
    • (2000) Russ. Chem. Bull. , vol.49 , pp. 659-665
    • Adam, W.1    Bronstein, I.2    Vasil'Ev, R.F.3    Trofimov, A.V.4
  • 112
    • 0033219241 scopus 로고    scopus 로고
    • Synthesis and chemiluminescent decomposition of spiro[1,2-dioxetane-3, 6′-benzo(c)chromene]s
    • Matsumoto, M., M. Kawahara, and, N. Watanabe, (1999) Synthesis and chemiluminescent decomposition of spiro[1,2-dioxetane-3,6′-benzo(c) chromene]s. Luminescence 14, 341-344.
    • (1999) Luminescence , vol.14 , pp. 341-344
    • Matsumoto, M.1    Kawahara, M.2    Watanabe, N.3
  • 113
    • 0033546235 scopus 로고    scopus 로고
    • Synthesis of thermally stable 1,2-dioxetanes bearing a phenylethenyl or a phenylethynyl moiety and their base-induced decomposition
    • Matsumoto, M., T. Ishihara, N. Watanabe, and, T. Hiroshima, (1999) Synthesis of thermally stable 1,2-dioxetanes bearing a phenylethenyl or a phenylethynyl moiety and their base-induced decomposition. Tetrahedron Lett. 40, 4571-4574.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 4571-4574
    • Matsumoto, M.1    Ishihara, T.2    Watanabe, N.3    Hiroshima, T.4
  • 114
    • 37049086885 scopus 로고
    • Thermal stability and chemiluminescence of 3-alkoxy-3-aryl-4,4- diisopropyl-l,2-dioxetanes
    • Matsumoto, M., H. Suganuma, Y. Katao, and, H. Mutoh, (1995) Thermal stability and chemiluminescence of 3-alkoxy-3-aryl-4,4-diisopropyl-l,2- dioxetanes. J. Chem. Soc., Chem. Commun. 431-432.
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 431-432
    • Matsumoto, M.1    Suganuma, H.2    Katao, Y.3    Mutoh, H.4
  • 115
    • 0031030444 scopus 로고    scopus 로고
    • Synthesis and chemiluminescence of 3,3-diisopropyl-4-methoxy-4-(2- naphthyl)-1,2-dioxetanes
    • Matsumoto, M., N. Watanabe, H. Kobayashi, M. Azami, and, H. Ikawa, (1997) Synthesis and chemiluminescence of 3,3-diisopropyl-4-methoxy-4-(2-naphthyl)-1, 2-dioxetanes. Tetrahedron Lett. 38, 411-414.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 411-414
    • Matsumoto, M.1    Watanabe, N.2    Kobayashi, H.3    Azami, M.4    Ikawa, H.5
  • 116
    • 0036726516 scopus 로고    scopus 로고
    • Synthesis of 5-tert-butyl-1-(3-tert-butyldimethylsiloxy)phenyl-4,4- dimethyl-2,6,7-dioxabicyclo[3.2.0]-heptanes and their fluoride-induced chemiluminescent decomposition: Effect of a phenolic electron donor on the CIEEL decay rate in aprotic polar solvent
    • Matsumoto, M., Y. Ito, M. Murakami, and, N. Watanabe, (2002) Synthesis of 5-tert-butyl-1-(3-tert-butyldimethylsiloxy)phenyl-4,4-dimethyl-2,6,7- dioxabicyclo[3.2.0]-heptanes and their fluoride-induced chemiluminescent decomposition: Effect of a phenolic electron donor on the CIEEL decay rate in aprotic polar solvent. Luminescence 17, 305-312.
    • (2002) Luminescence , vol.17 , pp. 305-312
    • Matsumoto, M.1    Ito, Y.2    Murakami, M.3    Watanabe, N.4
  • 117
    • 0038176371 scopus 로고    scopus 로고
    • Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter
    • Watanabe, N., Y. Nagashima, T. Yamazaki, and, M. Matsumoto, (2003) Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter. Tetrahedron 59, 4811-4819.
    • (2003) Tetrahedron , vol.59 , pp. 4811-4819
    • Watanabe, N.1    Nagashima, Y.2    Yamazaki, T.3    Matsumoto, M.4
  • 118
    • 17644409018 scopus 로고    scopus 로고
    • Bicyclic dioxetanes bearing an inden-2-yl or a benzo(b)thiazol-2-yl moiety as a CIEEL-active chemiluminescent substrate emitting red light
    • Watanabe, N., K. Nagamatsu, T. Mizuno, and, M. Matsumoto, (2005) Bicyclic dioxetanes bearing an inden-2-yl or a benzo(b)thiazol-2-yl moiety as a CIEEL-active chemiluminescent substrate emitting red light. Luminescence 20, 63-72.
    • (2005) Luminescence , vol.20 , pp. 63-72
    • Watanabe, N.1    Nagamatsu, K.2    Mizuno, T.3    Matsumoto, M.4
  • 119
    • 0029818914 scopus 로고    scopus 로고
    • Electron exchange luminescence of spiroadamantyl-substituted dioxetanes triggered by alkaline phosphatase. Kinetics and elucidation of pH effects
    • Adam, W., I. Bronstein, B. Edwards, T. Engel, D. Reinhardt, F. W. Schneider, A. V. Trofimov, and, R. F. Vasil'ev, (1996) Electron exchange luminescence of spiroadamantyl-substituted dioxetanes triggered by alkaline phosphatase. Kinetics and elucidation of pH effects. J. Am. Chem. Soc. 118, 10400-10407.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10400-10407
    • Adam, W.1    Bronstein, I.2    Edwards, B.3    Engel, T.4    Reinhardt, D.5    Schneider, F.W.6    Trofimov, A.V.7    Vasil'Ev, R.F.8
  • 120
    • 0005177029 scopus 로고
    • Base-induced chemiluminescence of acetoxy-substituted benzofuran dioxetanes by an intramolecular electron transfer (CIEEL) mechanism
    • Adam, W., and, M. H. Schulz, (1992) Base-induced chemiluminescence of acetoxy-substituted benzofuran dioxetanes by an intramolecular electron transfer (CIEEL) mechanism. Chem. Ber. 125, 2455-2461.
    • (1992) Chem. Ber. , vol.125 , pp. 2455-2461
    • Adam, W.1    Schulz, M.H.2
  • 121
    • 1842850685 scopus 로고    scopus 로고
    • Chemiluminescent decomposition of a dioxetane bearing a 3-(1-cyanoethenyl)phenyl moiety induced by michael addition of an anion of malonate
    • Matsumoto, M., T. Mizuno, and, N. Watanabe, (2004) Chemiluminescent decomposition of a dioxetane bearing a 3-(1-cyanoethenyl)phenyl moiety induced by michael addition of an anion of malonate. Tetrahedron Lett. 45, 3779-3782.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 3779-3782
    • Matsumoto, M.1    Mizuno, T.2    Watanabe, N.3
  • 122
    • 0037458945 scopus 로고    scopus 로고
    • Fluoride-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenyl moiety substituted with a methyl having an electron-withdrawing group
    • Matsumoto, M., T. Mizuno, and, N. Watanabe, (2003) Fluoride-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenyl moiety substituted with a methyl having an electron-withdrawing group. Chem. Commun. 482-483.
    • (2003) Chem. Commun. , pp. 482-483
    • Matsumoto, M.1    Mizuno, T.2    Watanabe, N.3
  • 123
    • 84873132820 scopus 로고    scopus 로고
    • 4 nanoparticles as oxidase mimic-mediated chemiluminescence of aqueous luminol for sulfite in white wines
    • 4 nanoparticles as oxidase mimic-mediated chemiluminescence of aqueous luminol for sulfite in white wines. J. Agric. Food Chem. 61, 840-847.
    • (2013) J. Agric. Food Chem. , vol.61 , pp. 840-847
    • Zhang, X.1    He, S.2    Chen, Z.3    Huang, Y.4
  • 124
    • 33947088605 scopus 로고
    • Determination of trace amounts of iron(II) using chemiluminescence analysis
    • Seitz, W. R., and, D. M. Hercules, (1972) Determination of trace amounts of iron(II) using chemiluminescence analysis. Anal. Chem. 44, 2143-2149.
    • (1972) Anal. Chem. , vol.44 , pp. 2143-2149
    • Seitz, W.R.1    Hercules, D.M.2
  • 125
    • 84873099373 scopus 로고    scopus 로고
    • Development of a generic assay for the determination of total trihydroxy-benzoate derivatives based on gold-luminol chemiluminescence
    • Giokas, D. L., D. C. Christodouleas, I. Vlachou, A. G. Vlessidis, and, A. C. Calokerinos, (2013) Development of a generic assay for the determination of total trihydroxy-benzoate derivatives based on gold-luminol chemiluminescence. Anal. Chim. Acta 764, 70-77.
    • (2013) Anal. Chim. Acta , vol.764 , pp. 70-77
    • Giokas, D.L.1    Christodouleas, D.C.2    Vlachou, I.3    Vlessidis, A.G.4    Calokerinos, A.C.5
  • 126
    • 0034611040 scopus 로고    scopus 로고
    • Chemiluminescence as diagnostic tool: A review
    • Dodeigne, C., L. Thunus, and, R. Lejeune, (2000) Chemiluminescence as diagnostic tool: A review. Talanta 51, 415-439.
    • (2000) Talanta , vol.51 , pp. 415-439
    • Dodeigne, C.1    Thunus, L.2    Lejeune, R.3
  • 127
    • 0028976417 scopus 로고
    • Stopped flow luminol chemiluminescence determination of Fe(II) and reducible iron in seawater at subnanomolar levels
    • O'Sullivan, D. W., A. K. Hanson Jr, and, D. R. Kester, (1995) Stopped flow luminol chemiluminescence determination of Fe(II) and reducible iron in seawater at subnanomolar levels. Mar. Chem. 49, 65-77.
    • (1995) Mar. Chem. , vol.49 , pp. 65-77
    • O'Sullivan, D.W.1    Hanson Jr., A.K.2    Kester, D.R.3
  • 128
    • 84865455557 scopus 로고    scopus 로고
    • Selective light-triggered chemiluminescence between fluorescent dyes and luminol, and its analytical application
    • Ma, M., F. Diao, X. Zheng, and, Z. Guo, (2012) Selective light-triggered chemiluminescence between fluorescent dyes and luminol, and its analytical application. Anal. Bioanal. Chem. 404, 585-592.
    • (2012) Anal. Bioanal. Chem. , vol.404 , pp. 585-592
    • Ma, M.1    Diao, F.2    Zheng, X.3    Guo, Z.4
  • 130
    • 0028874116 scopus 로고
    • Selective stopped-flow determination of manganese with luminol in the absence of hydrogen peroxide
    • Gaikwad, A., M. Silva, and, D. Perez-Bendito, (1995) Selective stopped-flow determination of manganese with luminol in the absence of hydrogen peroxide. Anal. Chim. Acta 302, 275-282.
    • (1995) Anal. Chim. Acta , vol.302 , pp. 275-282
    • Gaikwad, A.1    Silva, M.2    Perez-Bendito, D.3
  • 131
    • 77956935457 scopus 로고
    • The mechanism of catalytic chemiluminescence of luminol
    • (Edited by L. I. Simándi), Elsevier Science Publishers, Amsterdam
    • Ojima, H., and, K. Nonoyama, (1991) The mechanism of catalytic chemiluminescence of luminol. In Dioxygen Activation and Homogeneous Catalytic Oxidation. (Edited by, L. I. Simándi,), pp. 417-427. Elsevier Science Publishers, Amsterdam.
    • (1991) Dioxygen Activation and Homogeneous Catalytic Oxidation , pp. 417-427
    • Ojima, H.1    Nonoyama, K.2
  • 132
    • 0016543438 scopus 로고
    • Mechanism of cobalt catalysis of luminol chemiluminescence
    • Burdo, T. G., and, W. R. Seitz, (1975) Mechanism of cobalt catalysis of luminol chemiluminescence. Anal. Chem. 47, 1639-1643.
    • (1975) Anal. Chem. , vol.47 , pp. 1639-1643
    • Burdo, T.G.1    Seitz, W.R.2
  • 133
    • 0035894168 scopus 로고    scopus 로고
    • Chemiluminescence of luminol in the presence of iron(II) and oxygen: Oxidation mechanism and implications for its analytical use
    • Rose, A. L., and, T. D. Waite, (2001) Chemiluminescence of luminol in the presence of iron(II) and oxygen: Oxidation mechanism and implications for its analytical use. Anal. Chem. 73, 5909-5920.
    • (2001) Anal. Chem. , vol.73 , pp. 5909-5920
    • Rose, A.L.1    Waite, T.D.2
  • 134
    • 33947293770 scopus 로고
    • The chemiluminescence of organic hydrazides
    • White, E. H., and, D. F. Roswell, (1970) The chemiluminescence of organic hydrazides. Acc. Chem. Res. 3, 54-62.
    • (1970) Acc. Chem. Res. , vol.3 , pp. 54-62
    • White, E.H.1    Roswell, D.F.2
  • 135
  • 136
    • 0342383646 scopus 로고
    • Chemiluminescence of luminol and related compounds under e-beam excitation. Absolute chemical and light yields
    • Wurzberg, E., and, Y. Haas, (1978) Chemiluminescence of luminol and related compounds under e-beam excitation. Absolute chemical and light yields. Chem. Phys. Lett. 55, 250-253.
    • (1978) Chem. Phys. Lett. , vol.55 , pp. 250-253
    • Wurzberg, E.1    Haas, Y.2
  • 137
    • 84940810730 scopus 로고
    • Some aspects of the luminol light reaction
    • (Edited by W. D. McElroy and B. Glass), Johns Hopkins Press, Baltimore
    • Seliger, H. H., (1961) Some aspects of the luminol light reaction. In A Symposium on Light and Life. (Edited by, W. D. McElroy, and, B. Glass,), pp. 200-205. Johns Hopkins Press, Baltimore.
    • (1961) A Symposium on Light and Life , pp. 200-205
    • Seliger, H.H.1
  • 138
    • 33947089554 scopus 로고
    • Yields of chemically produced excited states
    • Brundrett, R. B., D. F. Roswell, and, E. H. White, (1972) Yields of chemically produced excited states. J. Am. Chem. Soc. 94, 7536-7541.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 7536-7541
    • Brundrett, R.B.1    Roswell, D.F.2    White, E.H.3
  • 139
    • 0008328603 scopus 로고
    • Determination of the chemiluminescence quantum yield of luminol in rapid chemical reactions
    • Lind, J., and, G. Merenyi, (1981) Determination of the chemiluminescence quantum yield of luminol in rapid chemical reactions. Chem. Phys. Lett. 82, 331-333.
    • (1981) Chem. Phys. Lett. , vol.82 , pp. 331-333
    • Lind, J.1    Merenyi, G.2
  • 140
    • 0033946807 scopus 로고    scopus 로고
    • Absolute calibration of luminometers with low-level light standards
    • O'Kane, D. J., and, J. Lee, (2000) Absolute calibration of luminometers with low-level light standards. Methods Enzymol. 305, 87-96.
    • (2000) Methods Enzymol. , vol.305 , pp. 87-96
    • O'Kane, D.J.1    Lee, J.2
  • 141
    • 34548747539 scopus 로고    scopus 로고
    • Development of a quantitative bioâchemiluminescence spectrometer determining quantum yields: Re-examination of the aqueous luminol chemiluminescence standard
    • Ando, Y., K. Niwa, N. Yamada, T. Irie, T. Enomoto, H. Kubota, Y. Ohmiya, and, H. Akiyama, (2007) Development of a quantitative bioâ chemiluminescence spectrometer determining quantum yields: Re-examination of the aqueous luminol chemiluminescence standard. Photochem. Photobiol. 83, 1205-1210.
    • (2007) Photochem. Photobiol. , vol.83 , pp. 1205-1210
    • Ando, Y.1    Niwa, K.2    Yamada, N.3    Irie, T.4    Enomoto, T.5    Kubota, H.6    Ohmiya, Y.7    Akiyama, H.8
  • 142
    • 63749098014 scopus 로고    scopus 로고
    • Bioinspired supramolecular confinement of luminol and heme proteins to enhance the chemiluminescent quantum yield
    • Wang, Q., L. Li, and, B. Xu, (2009) Bioinspired supramolecular confinement of luminol and heme proteins to enhance the chemiluminescent quantum yield. Chem. Eur. J. 15, 3168-3172.
    • (2009) Chem. Eur. J. , vol.15 , pp. 3168-3172
    • Wang, Q.1    Li, L.2    Xu, B.3
  • 143
    • 84981610960 scopus 로고
    • Quantum yields of the luminol chemiluminescence reaction in aqueous and aprotic solvents
    • Lee, J., and, H. H. Seliger, (1972) Quantum yields of the luminol chemiluminescence reaction in aqueous and aprotic solvents. Photochem. Photobiol. 15, 227-237.
    • (1972) Photochem. Photobiol. , vol.15 , pp. 227-237
    • Lee, J.1    Seliger, H.H.2
  • 144
    • 84981841093 scopus 로고
    • 1) Oxydation du 3-Aminophtalhydrazide
    • 1) Oxydation du 3-Aminophtalhydrazide. Bull. Soc. Chim. Belg. 62, 569-610.
    • (1953) Bull. Soc. Chim. Belg. , vol.62 , pp. 569-610
    • Bremer, T.1
  • 145
    • 0000295790 scopus 로고
    • Synthesis and chemiluminescence of derivatives of luminol and isoluminol
    • Brundrett, R. B., and, E. H. White, (1974) Synthesis and chemiluminescence of derivatives of luminol and isoluminol. J. Am. Chem. Soc. 96, 7497-7502.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 7497-7502
    • Brundrett, R.B.1    White, E.H.2
  • 146
    • 0012564698 scopus 로고
    • Chemiluminescent reactions of lucigenin. 2. Reactions of lucigenin with hydroxide ion and other nucleophiles
    • Maskiewicz, R., D. Sogah, and, T. C. Bruice, (1979) Chemiluminescent reactions of lucigenin. 2. Reactions of lucigenin with hydroxide ion and other nucleophiles. J. Am. Chem. Soc. 101, 5355-5364.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 5355-5364
    • Maskiewicz, R.1    Sogah, D.2    Bruice, T.C.3
  • 148
    • 0037131148 scopus 로고    scopus 로고
    • Peroxyoxalate chemiluminescence of N, N′-bistosyl-1H,4H-quino- xaline-2,3-dione and related compounds. Dependence on electronic nature of fluorophores
    • Motoyoshiya, J., N. Sakai, M. Imai, M. Yamaguchi, R. Koike, Y. Takaguchi, and, H. Aoyama, (2002) Peroxyoxalate chemiluminescence of N, N′-bistosyl-1H,4H-quino-xaline-2,3-dione and related compounds. Dependence on electronic nature of fluorophores. J. Org. Chem. 67, 761-765.
    • (2002) J. Org. Chem. , vol.67 , pp. 761-765
    • Motoyoshiya, J.1    Sakai, N.2    Imai, M.3    Yamaguchi, M.4    Koike, R.5    Takaguchi, Y.6    Aoyama, H.7
  • 149
    • 84871976853 scopus 로고    scopus 로고
    • The hammett correlation between distyrylbenzene substituents and chemiluminescence efficiency providing various ρ-values for peroxyoxalate chemiluminescence of several oxalates
    • Maruyama, T., S. Narita, and, J. Motoyoshya, (2013) The hammett correlation between distyrylbenzene substituents and chemiluminescence efficiency providing various ρ-values for peroxyoxalate chemiluminescence of several oxalates. J. Photochem. Photobiol. A 252, 222-231.
    • (2013) J. Photochem. Photobiol. A , vol.252 , pp. 222-231
    • Maruyama, T.1    Narita, S.2    Motoyoshya, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.