Recombination kinetics of triplet radical ion pairs adsorbed onto microcrystalline cellulose studied by diffuse-reflectance laser flash photolysis

Langmuir ◽  
1993 ◽  
Vol 9 (4) ◽  
pp. 1001-1008 ◽  
Author(s):  
Peter P. Levin ◽  
L. F. Vieira Ferreira ◽  
Silvia M. B. Costa

1992 ◽  
Vol 193 (6) ◽  
pp. 461-468 ◽  
Author(s):  
Peter P. Levin ◽  
L.F. Vieira Ferreira ◽  
Silvia M.B. Costa ◽  
I.V. Katalnikov


2004 ◽  
Vol 6 (4) ◽  
pp. 205-213 ◽  
Author(s):  
A. S. Oliveira ◽  
L. F. Vieira Ferreira ◽  
J. P. Da Silva ◽  
J. C. Moreira

Ground-state diffuse reflectance, time resolved laser-induced luminescence, diffuse reflectance laser flash-photolysis transient absorption and chromatographic techniques were used to elucidate the photodegradation processes of pyrene adsorbed onto microcrystalline cellulose and silica. Ground-state diffuse reflectance showed that on both substrates low concentrations display absorption of pyrene monomers. At high concentrations spectral changes attributed to aggregate formation were observed. Laser induced fluorescence showed that pyrene onto microcrystalline cellulose mainly presents fluorescence from monomers, while for silica, excimer-like emission was observed from low surface loadings (≥0.5μmolg−1). Transient absorption and photodegradation studies were performed at concentrations where mainly monomers exist. On silica, pyrene presents transient absorption from its radical cation. On microcrystalline cellulose both radical cation, radical anion and pyrene triplet-triplet absorption were detected. Irradiation followed by chromatographic analysis showed that pyrene decomposes on both substrates. For pyrene on microcrystalline cellulose 1-hydroxypyrene was the main identified photoproduct since in the absence of oxygen further oxidation of 1-hydroxypyrene was very slow. For pyrene on silica photodegradation was very efficient. Almost no 1-hydroxypyrene was detected since in the presence of oxygen it is quickly oxidized to other photooxidation products. On both substrates, pyrene radical cation is the intermediate leading to photoproducts and oxygen it is not involved in its formation.





1983 ◽  
Vol 22 (8) ◽  
pp. 625-627 ◽  
Author(s):  
Nicholas J. Turro ◽  
David A. Hrovat ◽  
Ian R. Gould ◽  
Albert Padwa ◽  
William Dent ◽  
...  


2018 ◽  
Vol 20 (34) ◽  
pp. 22218-22227 ◽  
Author(s):  
N. U. M. Howes ◽  
Z. S. Mir ◽  
M. A. Blitz ◽  
S. Hardman ◽  
T. R. Lewis ◽  
...  

Kinetics of CH2OO + SO2 confirmed over a wide range of [SO2]. Acetaldehyde observed as a major product of the reaction of CH3CHOO + SO2.



RSC Advances ◽  
2020 ◽  
Vol 10 (42) ◽  
pp. 24817-24829 ◽  
Author(s):  
Janina Kabatc ◽  
Katarzyna Iwińska ◽  
Alicja Balcerak ◽  
Dominika Kwiatkowska ◽  
Agnieszka Skotnicka ◽  
...  

The chemical mechanisms were investigated by steady state photolysis and nanosecond laser flash photolysis experiments. A mechanism for initiating polymerization using both onium salts is proposed here.



Sign in / Sign up

Export Citation Format

Share Document