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IR 144
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Lougnot, D.J.; Lepaja, S.; Fouassier, J.P.
J. Chim. Phys. Phys.-Chim. Biol. 79, 617-628 (1982)
Reaction: 2-[2-[3-[[1,3-dihydro-1,1-dimethyl-3-(3-sulfopropyl)benz[e]indol-2-ylidene]ethylidene]-2-[4-(ethoxycarbonyl)-1-piperidinyl]-1-cyclopenten-1-yl]ethenyl[-1,1-dimethy3-(3-sulfopropyl)benz[e]indolium, hydroxide, inner salt, compound with triethylamine + 1O2* ®
products
Solvent: DMSO
kreact = 1.7 × 106(L mol-1 s-1), T = 295K
Experimental method: Photolysis
Analytical method: colorimetry
Data type: Derived from steady state measurements
Excitation wavelength: 514 nm
Photosensitizer = Thionine; used solvent kd = 1.3 × 104 s-1; used singlet oxygen quantum yield for sensitizer = 0.87.
Lougnot, D.J.; Lepaja, S.; Fouassier, J.P.
J. Chim. Phys. Phys.-Chim. Biol. 79, 617-628 (1982)
Reaction: 2-[2-[3-[[1,3-dihydro-1,1-dimethyl-3-(3-sulfopropyl)benz[e]indol-2-ylidene]ethylidene]-2-[4-(ethoxycarbonyl)-1-piperidinyl]-1-cyclopenten-1-yl]ethenyl[-1,1-dimethy3-(3-sulfopropyl)benz[e]indolium, hydroxide, inner salt, compound with triethylamine + 1O2* ®
products
Solvent: CH3OH
kreact = 1.0 × 107(L mol-1 s-1), T = 295K
Experimental method: Photolysis
Analytical method: colorimetry
Data type: Derived from steady state measurements
Excitation wavelength: 514 nm
Photosensitizer = Thionine; used solvent kd = 1.4 × 105 s-1; used singlet oxygen quantum yield for sensitizer = 0.87.