Oxygen, effect quantum yield

Hurley and Testa (Ref 17) exposed nitrobenzene in isopropyl alcohol, degassed and in air, to a mercury lamp at 3660A Products in the absence of air were acetone and phenyl-hydroxylamine (PHA). In air PHA was oxidized to nitro sob enzene which couples with PHA to form azoxybenzene. They hypothesized that the triplet molecule abstracted H-atoms from the solvent no effect was noted with ben zene as solvent. They also worked with nitrobenzene in isopropyl alcohol-water mixts containing HC1 with a mercury lamp at 3660A (Ref 18), and found that the quantum yields depended on pH and isopropyl alcohol content, but were independent of oxygen with acid present. Their conclusion was that the quantum yield consisted of two parts, H abstraction by the triplet, and protonation of the triplet... 

While the covalent attachment of cyanine dyes such as Cy5 or Alexa 647 to proteins does not result in noticeable changes in their spectral properties, squaraine dyes (oxo-squarines and squaraines with substituted squaraine oxygens) behave quite the opposite the absorption and emission maxima of squaraines are in general red-shifted after binding to proteins and the quantum yields and fluorescence lifetimes are manifold increased [68-70]. In general hydrophobic squaraines exhibit more pronounced increases compared to hydrophilic dyes. These effects are even stronger in noncovalent dye-protein complexes. Importantly, the photostability of squaraines also increases after binding to proteins. 

The ruthenium(II) polypyridyl complexes are also popular but the brightnesses do not exceed 15,000 and thermal quenching is rather significant. This property can be utilized to design temperature-sensitive probes providing that the dyes are effectively shielded from oxygen (e.g., in polyacrylonitrile beads). Despite often very high emission quantum yields the visible absorption of cyclometallated complexes of iridium(III) and platinum(II) is usually poor (e < 10,000 M-1cm-1), thus,... 

As mentioned above, phosphorescence is observed only under certain conditions because the triplet states are very efficiently deactivated by collisions with solvent molecules (or oxygen and impurities) because their lifetime is long. These effects can be reduced and may even disappear when the molecules are in a frozen solvent, or in a rigid matrix (e.g. polymer) at room temperature. The increase in phosphorescence quantum yield by cooling can reach a factor of 103, whereas this factor is generally no larger than 10 or so for fluorescence quantum yield. 

The effectiveness of various PS proposed for antimicrobial PDT can be judged on several criteria. These PS should be able to kill multiple classes of microbes at relatively low concentrations and low fluences of hght. PS should be reasonably nontoxic in the dark and should demonstrate selectivity for microbial cells over mammalian cells. PS should ideally have large extinction coefficients in the red part of the spectrum and demonstrate high triplet and singlet oxygen quantum yields. 

The cytotoxic and photocytotoxic effects of two water-soluble fullerene derivatives, a dendritic CL mono-adduct and the malonic acid CL tris-adduct were tested on Jurkat cells when irradiated with UVA or UVB light (Rancan et al., 2002). The cell death was mainly caused by membrane damage and it was UV dose-dependent. Tris-malonic acid fullerene was found to be more phototoxic than the dendritic derivative. This result is in contrast to the singlet oxygen quantum yields determined for the two compounds. 

Carbon disulfide quenches the fluorescence of anthracene quite efficiently,145,149 but seems to have little effect on its triplet lifetime.147 Diphenylanthracene in benzene fluoresces with a quantum yield of 0.8 and shows a high sensitivity to the oxygen concentration in photooxygenation reactions. With about 1 vol% of CS2 present, AC>2 is practically independent of [02] (> 10"5 mole/liter). In jjoth cases, where carbon disulfide was either used as solvent or was added to an otherwise strongly fluorescent solution, the quantum yields of photooxygenation followed... 

Quantum yields were determined, and the mechanism was discussed as a function of the temperature of the reaction, the structure of the substrate, and the effect of the dissolved oxygen. The formation of the 4- and 6-O-benzoyl derivatives 65 and 66 was later confirmed,87 and preliminary experiments conducted on methyl 2,3 4,6-di-0-ben-zylidene-a-D-mannopyranoside and on methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-a-D-gluco- and -galacto-pyranosides were reported.88 Further results in the field were obtained for an O-ethylidene deriva-... 

What are the effects of a rigid polymer matrix and of oxygen on the fluorescence lifetime and quantum yield ... 

Distilled rather than natural water is often used as the solvent for determination of quantum yields for two major reasons. First, the total absorbance of the solution at the wavelength of irradiation should not exceed 0.02. Second, and more important, the presence of natural water constituents (e.g., humic material, nitrate) could enhance the total photolytic transformation rate by indirect photolytic processes as described in Chapter 16. Zepp and Baughman (1978) have argued that for many chemicals d>,r obtained in distilled water is nearly the same as that observed in natural waters (at least in uncontaminated freshwaters), because concentrations of natural water constituents that could undergo reactions with or quench photolysis of excited pollutants are generally very low. Furthermore, the effects of molecular oxygen, which may act as a quencher, can also be studied in distilled water. 

The localization of the sensitizer has a significant effect on the photodynamic activity. Eosin is scarcely taken up by cells, and Pooler and Girotti [131] report that Eosin isothiocyanate is 50-100 times more efficient for inducing photohemolysis of human erythrocytes. The spectral properties and quantum yields for singlet oxygen production are identical for both compounds. Therefore, they attribute the difference in photodynamic activity to the ability of the isothiocyanate derivative to bind covalently to band 3 protein. 

A number of workers have looked at the effect of photooxidation and photodynamic sensitizers on DNA. Rose Bengal photosensitizes strand breaks in double-stranded, supercoiled, pBR322 DNA the effect follows first-order kinetics with respect to light fluence and dye concentration. The reaction is substantially more efficient in the absence of oxygen, but the quantum yield of strand breaks in air is only 10 8. The results are consistent with the initiation of chain scission by Rose Bengal triplet, with some additional mechanism coming into play in the presence of oxygen. 

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