A quantum yield determination of O(1D) production from ozone via laser flash photolysis

1977 ◽  
Vol 67 (7) ◽  
pp. 3316-3321 ◽  
Author(s):  
D. L. Philen ◽  
R. T. Watson ◽  
D. D. Davis
Keyword(s):  
Quantum Yield ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash ◽  
Yield Determination

Laser flash photolysis determination of absolute rate constants for reactions of bromine atoms in solution

1993 ◽  
Vol 115 (18) ◽  
pp. 8340-8344 ◽  
Author(s):  
J. C. Scaiano ◽  
M. Barra ◽  
M. Krzywinski ◽  
R. Sinta ◽  
G. Calabrese
Keyword(s):  
Rate Constants ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash ◽  
Absolute Rate

Photochemistry of α-chloro- and α-bromoacetophenone. Determination of extinction coefficients for halogen–benzene complexes

1988 ◽  
Vol 66 (6) ◽  
pp. 1474-1478 ◽  
Author(s):  
W. G. McGimpsey ◽  
J. C. Scaiano
Keyword(s):  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Benzene Solution ◽  
Halogen Bond ◽  
Bond Cleavage ◽  
Laser Flash ◽  
Quantum Yields ◽  
Extinction Coefficients ◽  
Transient Data

The photochemical dehalogenation of α-haloacetophenones (Cl, Br) in benzene solution has been examined under conditions of continuous and pulsed laser irradiation. Product and quantum yield studies indicate that carbon-halogen bond cleavage occurs with quantum yields of 0.88 and 0.41 for α-chloro- and α-bromoacetophenone, respectively. These values are based on trapping studies in which the PhC(O)ĊH2 radicals produced photochemically are scavenged by hydrogen donors such as benzenethiol. Laser flash photolysis studies lead to intense transient signals due to benzene–halogen complexes. Combination of transient data and quantum yields lead to extinction coefficients of 1 800 and 23 700 M−1 cm−1 for the chlorine (490 nm) and bromine (550 nm) complexes, respectively.

Laser flash photolysis: Quantum yield of O(1D) formation from ozone

1977 ◽  
Vol 24 (2) ◽  
pp. 211-217 ◽  
Author(s):  
I. Arnold ◽  
F.J. Comes ◽  
G.K. Moortgat
Keyword(s):  
Quantum Yield ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash

Substituted Phosphorous Triazatetrabenzocorroles: Correlation Between Structure and Excited State Properties

2009 ◽  
Vol 62 (5) ◽  
pp. 434 ◽  
Author(s):  
Xian-Fu Zhang ◽  
Yakuan Chang ◽  
Yanling Peng ◽  
Fushi Zhang
Keyword(s):  
Quantum Yield ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Photophysical Properties ◽  
Laser Flash ◽  
Time Resolved Fluorescence ◽  
Absorption Properties ◽  
Strong Electron ◽  
Time Resolved ◽  
Triplet Formation

The photophysical properties of five novel phthalocyanine analogues, dihydroxy phosphorus(v) triazatetrabenzocorrole (PTBC) substituted with –NO2, –SO3H, OiPr, and –NH2, respectively, were studied by a combination of absorption, steady-state emission, time-resolved fluorescence, and laser flash photolysis. All substituents, even for the strong electron-donating –NH2, cause only a slight red shift of their absorption and emission maxima. These complexes are generally monomeric in organic solution, whereas the sulfonated derivative, PTBC(SO3H)4, slightly aggregates in aqueous buffer. Distinct from phthalocyanines, PTBCs substituted with –NO2 or –NH2 still show high photo activities. The electron-withdrawing –NO2 and –SO3H decrease the fluorescence quantum yield but increase the triplet formation yield to 0.76 and 0.82, respectively. All PTBCs have long triplet lifetimes and hence generate singlet oxygen efficiently with a quantum yield from 0.43 to 0.75. Together with the ground-state absorption properties, the results suggest that these PTBCs may be used as excellent photosensitizers for photodynamic therapy.

scholarly journals Measurement of OH reactivity by laser flash photolysis coupled with laser-induced fluorescence spectroscopy

2016 ◽  
Author(s):  
Daniel Stone ◽  
Lisa K. Whalley ◽  
Trevor Ingham ◽  
Peter M. Edwards ◽  
Daniel R. Cryer ◽  
...  
Keyword(s):  
Loss Rate ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash ◽  
Laser Induced Fluorescence ◽  
Ozone Production ◽  
Oh Radicals ◽  
Field Campaigns ◽  
Lif Spectroscopy

Abstract. OH reactivity (k'OH) is the total pseudo-first-order loss rate coefficient describing the removal of OH radicals to all sinks in the atmosphere, and is the inverse of the chemical lifetime of OH. Measurements of ambient OH reactivity can be used to discover the extent to which measured OH sinks contribute to the total OH loss rate. Thus, OH reactivity measurements enable determination of the comprehensiveness of measurements used to predict air quality and ozone production, and, in conjunction with measurements of OH radical concentrations, to assess our understanding of OH production rates. In this work, we describe the design and characterisation of an instrument to measure OH reactivity using laser flash photolysis coupled to laser-induced fluorescence (LFP-LIF) spectroscopy. The LFP-LIF technique produces OH radicals in isolation, and thus minimises potential interferences in OH reactivity measurements owing to the reaction of HO2 with NO which can occur if HO2 is co-produced with OH in the instrument. Capabilities of the instrument for ambient OH reactivity measurements are illustrated by data collected during field campaigns in London, UK, and York, UK. We also present the coupling and characterisation of the LFP-LIF instrument to an atmospheric chamber for measurements of OH reactivity during simulated experiments, and provide suggestions for future improvements to OH reactivity LFP-LIF instruments.

Determination of rate constants for some reactions of CBr radicals by VUV laser flash photolysis

1983 ◽  
Vol 80 (3) ◽  
pp. 345-350 ◽  
Author(s):  
L. Hellner ◽  
K.T.V. Grattan ◽  
M.H.R. Hutchinson
Keyword(s):  
Rate Constants ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash
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