Quantum yield transfer

Hunt, JP Taube, H. The photoehemieal deeomposition of hydrogen peroxide, Quantum yields, transfer and fraetionation effeets. Journal of American Chemical Society, 1952 74, 5999-6002. 

Goelenterate. Coelenterates Penilla reformis (sea pansy) -cradViequoreaforskalea (jelly fish) produce bioluminescence by similar processes (223). The basic luciferin stmcture is (49) (224) and excited amide (50) is the emitter. The stmctural relationship to Varela is evident. A stmctural analogue where R = CH is active ia bioluminescence. The quantum yield is about 4% (223), with at 509 nm (56). This reaction iavolves a charge transfer between green fluorescent proteia and the excited-state coelenterate oxylucifetin. 

Irradiation of coordination compounds in the charge-transfer spectral region can often enhance redox reactions. The quantum yields are variable. 

In 2-propanoI, the quantum yield for photolytic conversion of benzophenone to the coupled reduction product is 2.0. The reason is that the radical remaining after abstraction of a hydrogen atom from 2-propanol transfers a hydrogen atom to ground-state benzophenone in a nonphotochemical reaction. Because of this process, two molecules of benzophenone are reduced for each one that is photoexcited ... 

The electron transfer step is typically fast and efficient. Griller et a/.292 measured absolute rate constants for decay of benzophenone triplet in the presence of aliphatic tertiary amines in benzene as solvent. Values lie in die range 3-4x109 M 1 s 1 and quantum yields are close to unity. 

The fluorescent lifetime of chlorophyll in vivo was first measured in 1957, independently by Brody and Rabinowitch (62) using pulse methods, and by Dmitrievskyand co-workers (63) using phase modulation methods. Because the measured quantum yield was lower than that predicted from the measured lifetime, it was concluded that much of the chlorophyll molecule was non-fluorescent, suggesting that energy transfer mechanisms were the means of moving absorbed energy to reactive parts of the molecule. 

Definition and Uses of Standards. In the context of this paper, the term "standard" denotes a well-characterized material for which a physical parameter or concentration of chemical constituent has been determined with a known precision and accuracy. These standards can be used to check or determine (a) instrumental parameters such as wavelength accuracy, detection-system spectral responsivity, and stability (b) the instrument response to specific fluorescent species and (c) the accuracy of measurements made by specific Instruments or measurement procedures (assess whether the analytical measurement process is in statistical control and whether it exhibits bias). Once the luminescence instrumentation has been calibrated, it can be used to measure the luminescence characteristics of chemical systems, including corrected excitation and emission spectra, quantum yields, decay times, emission anisotropies, energy transfer, and, with appropriate standards, the concentrations of chemical constituents in complex S2unples. 

On the other hand. Type II process competes efficiently with the electron-transfer pathway in aerobic environments where the concentration of ground triplet state molecular oxygen is relatively high ( 0.27 mM), and singlet molecular oxygen (1O2) is the most abimdant ROS generated under these conditions, with a quantum yield 0.48 (Valle et al., 2011), eqn. 8. It is also possible an electron-transfer reaction from 3RF to 02 to form anion superoxide, but this reaction occurs with very low efficiency <0.1% (Lu et al., 2000). 

The LIF technique is extremely versatile. The determination of absolute intermediate species concentrations, however, needs either an independent calibration or knowledge of the fluorescence quantum yield, i.e., the ratio of radiative events (detectable fluorescence light) over the sum of all decay processes from the excited quantum state—including predissociation, col-lisional quenching, and energy transfer. This fraction may be quite small (some tenths of a percent, e.g., for the detection of the OH radical in a flame at ambient pressure) and will depend on the local flame composition, pressure, and temperature as well as on the excited electronic state and ro-vibronic level. Short-pulse techniques with picosecond lasers enable direct determination of the quantum yield [14] and permit study of the relevant energy transfer processes [17-20]. 

In dichloromethane solutions, excitation of the chromophoric groups of the dendrons causes singlet-singlet energy transfer processes that lead to the excitation of the porphyrin core. It was found that the dendrimer 17, which has a spherical morphology, exhibits a much higher energy transfer quantum yield (0.8) than the partially substituted species 13-16 (quantum yield <0.32). Fluo-... 

It is interesting to note that some reactions proceed with large quantum yield, e.g.

transfer mechanisms so that little interference between anodic and cathodic processes occurs . ... 

As a rule, high quantum yields for two-electron transfer reactions are expected when the mechanism is one-electron/two-hole or two-electron/one-hole. In the cases of twQ-electron/two-hole or one-electron/one-hole efficient back reactions of the intermediates on the colloidal particles or in solution, respectively, will lead to a low yield of the final products. 

Nosaka and Fox determined the quantum yield for the reduction of methyl viologen adsorbed on colloidal CdS particles as a function of incident light intensity. Electron transfer from CdS to MV " competes with electron-hole recombination. They derived a bimolecular rate constant of 9 10 cm s for the latter process. 

Instead of postulating Zn," as intermediate, as it has a highly negative potential and is possibly unstable in ZnO, one may write the above mechanism with Zn e pairs. The blue-shift in the absorption upon illumination was explained by the decrease in particle size. The Hauffe mechanism was abandoned after it was recognized that an excess electron on a colloidal particle causes a blue-shift of the absorption threshold (see Fig. 19). In fact, in a more recent study it was shown that the blue-shift is also produced in the electron transfer from CH2OH radicals to colloidal ZnO particles When deaerated propanol-2 solutions of colloidal ZnO were irradiated for longer times, a black precipitate of Zn metal was formed. In the presence of 10 M methyl viologen in the alcohol solution, MV was produced with a quantum yield of 80 %... 

The quantum yield for the formation of 8-oxodGuo 44 from guanine in relation to the formation of products arising from the oxidation of other nucle-obases may be considered as a marker of charge transfer efficiency. This parameter was therefore used to study the influence of duplex stability on... 

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