Chemiluminescent 1,2-dioxetane compounds

Details Chemiluminescent 1,2-dioxetane compounds Chemiluminescent 1,2-dioxetane compounds

1987-03-09

1998-01-13

Owens, Amelia A.

Compositions

Chemiluminescent

549332, 549510, 568308, 568309, 568322, 435 6, 435 71, 435 18, 435 19, 435 21, 435125, 435147, 435148, C09K 300, C07C 49213

Patent

active

057075590

ABSTRACT:
Novel light producing 1,2-dioxetanes are described of the formula ##STR1## wherein ArOX is an aryl ring substituted with an X oxy group and A are passive organic groups which allow the 1,2-dioxetane to produce light when triggered by removing X. X is a chemically labile group which is removed by an activating agent. The 1,2-dioxetane compounds can be triggered to produce light at room temperatures.

REFERENCES:
patent: 2478377 (1949-08-01), Dickey
patent: 3009962 (1961-11-01), Milas
patent: 3442813 (1969-05-01), Bollyky
patent: 3442814 (1969-05-01), Sheehan
patent: 3470103 (1969-09-01), Sheehan
patent: 3597362 (1971-08-01), Bolllyky
patent: 3677957 (1972-07-01), Maulding
patent: 3720622 (1973-03-01), Bollyky
patent: 3763188 (1973-10-01), Krespan
patent: 3862142 (1975-01-01), Story
patent: 4302534 (1981-11-01), Halamann
patent: 4315998 (1982-02-01), Neckers et al.
patent: 4372745 (1983-02-01), Mandle
patent: 4446233 (1984-05-01), Auditore-Hargr
patent: 4663278 (1987-05-01), DiNello
patent: 4665018 (1987-05-01), Vold
F. McCapra, Chem. Commin., 155 (1968).
Shimomura, O., et al., Photochem. Photobiol., 30, 89 (1979).
Kopecky et al., Can. J. Chem., 47, 709 (1969).
Bartlett, et al., J. Amer. Chem. Soc., 92, 3223 (1970).
Mazur et al., J. Amer. Chem. Soc., 92, 3225 (1970).
Schaap, et al., J. Amer, Chem. Soc., 99, 1270 (1977).
Zaklika, et al., J. Amer. Chem. Soc., 100, 318 (1978) / & J. Amer. Chem. Soc., 100,4916 (1978).
Zaklita, et al., Photochem. Photobiol., 30, 35 (1979).
Schaap, et al., Organic Photochemical Synthesis,II, 49 (1976).
Schaap, et al., J. Amer. Chem. Soc., 101, 4016 (1979), & J. Amer. Chem Soc., 97,3741 (1975).
Wieringa, et al., Tetrahedron Lett., 169 (1972).
Turro, et al., J. Amer. Chem. Soc., 97, 7110 (1975).
Adam, et al., Z. Natuforsch., 39b, 679 (1984).
Wynberg, et al., In Bioluminescence & Chemiluminescence, DeLuca and McElroy (Eds.) Academic Press, N.Y. p. 687, 1981.
McCapra, et al., J. Chem. Soc., Chem. Commun., 944 (1977).
Adam,W., et al, Chem. Ber., 116, 839 (1983).
Geller,G.G., et al., Tetrahedron Lett., 673 (1983).
Schaap, et al., Tetrahedron Lett., 2943 (1982).
Handley, R.S., et al., Tetrahedron Lett., 3183 (1985).
Schaap, et al., J. Amer. Chem. Soc., 104, 3504 (1982).
Corey, et al., J. Amer. Chem. Soc., 94, 6190 (1972).
Kricka, L.J., Ligand-Binder Assays, Marcel Dekker, Inc., N.Y., pp. 170 & 199 (1985).
Sunthankar, et al., J. Org. Chem., 16, 8 (1951).
Patolia & Trivedi, Indian J. Chem., 22B 444 (1983).
Davies, et al., J. Org. Chem., 23, 307 (1958).
Wilson, T., et al., J. Amer. Chem. Soc., 93, 4126 (1971).
McMurry et al., J. Org. Chem. vol. 42, No. 15, 2655-2656 (1977).
McMurry et al., J. Org. Chem., vol. 43, No. 17, 3255-3266 (1978).
Physical Chemistry, Series Two vol. 9 Chemical Kinetics pp. 302-303.
Wilson, et al. JACS 95:14, Jul. 11, 1973 "Solvent Effects".
Bartlett et al, JACS 96:17, Aug. 21, 1974 "Metal Ion Catalysed".

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