N-[5-Hydroxy-8-[[2-(methylsulfonyl)-4-nitrophenyl]azo]-1-naphthalenyl-1,3-benzenedisulfonamide, conjugate base
Singlet oxygen


Merkel, P.B.; Smith, W.F.,Jr.
J. Phys. Chem. 83, 2834-2840 (1979)

Reaction: N-[5-Hydroxy-8-[[2-(methylsulfonyl)-4-nitrophenyl]azo]-1-naphthalenyl-1,3-benzenedisulfonamide, conjugate base + 1O2* ® physical quenching
Solvent: DMF

kquen = 5.6 × 107(mol L-1)

Experimental method: Photolysis
Analytical method: vis-UV absorption
Data type: Derived from steady state measurements

Photosensitizer = Rose Bengal dianion; used solvent kd = 7.1 × 104 s-1. Includes possible back energy transfer; kprod. = 9.3 × 106 L/(mol·s) derived using singlet oxygen quantum yield = 0.4; soln. contains NH4OH.


Merkel, P.B.; Smith, W.F.,Jr.
J. Phys. Chem. 83, 2834-2840 (1979)

Reaction: N-[5-Hydroxy-8-[[2-(methylsulfonyl)-4-nitrophenyl]azo]-1-naphthalenyl-1,3-benzenedisulfonamide, conjugate base + 1O2* ® products
Solvent: H2O

kreact = 1.3 × 108(L mol-1 s-1)

Experimental method: Photolysis
Analytical method: vis-UV absorption
Data type: Derived from steady state measurements

Self-sensitized; used solvent kd = 3.3 × 105 s-1; used singlet oxygen quantum yield = 1.3 × 10-4; soln. contains NH4OH.


Merkel, P.B.; Smith, W.F.,Jr.
J. Phys. Chem. 83, 2834-2840 (1979)

Reaction: N-[5-Hydroxy-8-[[2-(methylsulfonyl)-4-nitrophenyl]azo]-1-naphthalenyl-1,3-benzenedisulfonamide, conjugate base + 1O2* ® physical quenching
Solvent: CH3OH

kquen = 7.2 × 107(mol L-1)

Experimental method: Photolysis
Analytical method: vis-UV absorption
Data type: Derived from steady state measurements

Self-sensitized; used solvent kd = 1.3 × 105 s-1; kq includes possible back energy transfer; kprod. = 4.8 × 106 L/(mol·s) derived using singlet oxygen quantum yield = 1.6 × 10-3; soln. contains NH4OH.


See also N-[5-Hydroxy-8-[[2-(methylsulfonyl)-4-nitrophenyl]azo]-1-naphthalenyl-1,3-benzenedisulfonamide, conjugate dibase
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