Redox reactions of manganese porphyrins in aqueous solutions. Steady-state and pulse radiolysis spectrophotometric studies

1984 ◽  
Vol 88 (8) ◽  
pp. 1575-1579 ◽  
Author(s):  
K. M. Morehouse ◽  
P. Neta
2000 ◽  
Vol 41 (4) ◽  
pp. 355-366 ◽  
Author(s):  
SUDHIR KAPOOR ◽  
ROBIN MATHEW ◽  
NAGARAJ G. HUILGOL ◽  
TSUTOMU V. KAGIYA ◽  
CHERUPALLY KRISHNAN K. NAIR

1994 ◽  
Vol 98 (38) ◽  
pp. 9565-9569 ◽  
Author(s):  
K. I. Priyadarsini ◽  
H. Mohan ◽  
J. P. Mittal ◽  
D. M. Guldi ◽  
K.-D. Asmus

1970 ◽  
Vol 48 (2) ◽  
pp. 393-394 ◽  
Author(s):  
W. A. Seddon ◽  
M. J. Young

Pulse radiolysis of aqueous solutions of nitric oxide at neutral pH shows that the reaction initiated by the hydrated electron, e−(aq), proceeds via NO− and a new transient thought to be (N2O2)−, and not HNO as indicated previously by steady state radiolysis.


1996 ◽  
Vol 146 (5) ◽  
pp. 514 ◽  
Author(s):  
K. Chabita ◽  
A. Saha ◽  
P. C. Mandal ◽  
S. N. Bhattacharyya ◽  
M. C. Rath ◽  
...  

2002 ◽  
Vol 43 (1) ◽  
pp. 99-99 ◽  
Author(s):  
SUDHIR KAPOOR ◽  
TULSI MUKHERJEE ◽  
TSUTOMU V. KAGIYA ◽  
CHERUPALLY KRISHNAN K. NAIR

Pulse radiolysis supplemented by steady state radiolysis of aqueous solutions containing some of the following solutes: N 2 O, Br - , BrO - , BrO - 2 , BrO - 3 , CO 2- 3 , and OH - has been used to identify the absorption spectra of BrO ( λ max = 350 nm) and BrO 2 ( λ max = 475 nm) and to evaluate the following rate constants (units, M -1 s -1 ): e - aq. + BrO - → Br - + O - (2.3 ± 0.5 x 10 10 ); e - aq. + BrO - 2 → BrO + O 2- (1.8 ± 0.2 x 10 10 ); e - aq. + BrO - 3 → BrO 2 + O 2- (4.1 ± 0.2 x 10 9 ); OH + BrO - → OH - + BrO (4.5 x 10 9 ); O - + BrO - → BrO + O 2- (4.6 x 10 9 ); OH + BrO - 2 → OH - + BrO 2 (1.9 x 10 9 ); Br - 2 + BrO - → BrO + 2Br - (8.0 ± 0.7 x 10 7 ); Br - 2 + BrO - 2 → BrO + Br - + BrO - (8.0 ± 0.8 x 10 7 ); BrO + BrO - 2 → BrO - + BrO 2 (3.4 ± 0.7 x 10 8 ); 2BrO 2 ⇌ Br 2 O 4 ( k = 1.4 x 10 9 and K = 19 M -1 ); Br 2 O 4 + OH - → H + + BrO - 2 + BrO - 3 (7 x 10 8 ); 2BrO + H 2 O → BrO - + BrO - 2 + 2H + (4.9 ± 1.0 x10 9 ); CO - 3 + BrO - → CO 2- 3 + BrO (4.3 ± 0.4 x 10 7 ); CO - 3 + BrO - 2 → CO 2- 3 + BrO 2 (1.1 ± 0.1 x 10 8 ). In contrast to their chlorine analogues, little is known of the chemistry of the bromine oxides in aqueous solution. In this paper we describe the methods of formation and identification of the radicals BrO and BrO 2 , and their reactions with various oxybromine species, as elucidated by the techniques of pulse radiolysis and kinetic spectroscopy applied to aqueous solutions containing oxybromine anions.


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