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Excited states photosensitization

Alternatively, light is consumed and the reaction progress is possible only under continuous light absorption this option, called catalyzed photolysis, includes photoassisted generation of a reactive form of substrate or photocatalyst. In the former the process is called catalyzed photochemical reaction, whereas in the latter either catalyst activation may lead to formation of catalyst or photoinitiator, which initiates chemical transformations but is consumed within a reaction cycle, or the catalyst reacts with substrate in its excited state (photosensitization) in both cases... [Pg.63]

Intermolecular Physical Processes of Excited States Photosensitization Processes... [Pg.195]

Photosensitization is an important alternative to direct excitation of molecules, and this method of excitation usually results in reactions that occur via triplet excited states. If... [Pg.745]

Aromatic compounds such as toluene, xylene, and phenol can photosensitize cis-trans interconversion of simple alkenes. This is a case in which the sensitization process must be somewhat endothermic because of the energy relationships between the excited states of the alkene and the sensitizers. The photostationary state obtained under these conditions favors the less strained of the alkene isomers. The explanation for this effect can be summarized with reference to Fig. 13.12. Isomerization takes place through a twisted triplet state. This state is achieved by a combination of energy transfer Irom the sensitizer and thermal activation. Because the Z isomer is somewhat higher in energy, its requirement for activation to the excited state is somewhat less than for the E isomer. If it is also assumed that the excited state forms the Z- and -isomers with equal ease, the rate of... [Pg.769]

Alkyl derivatives of 1,3-butadiene usually undergo photosensitized Z-E isomerism when photosensitizers that can supply at least 60 kcal/mol are used. Two conformers of the diene, the s-Z and s-E, exist in equilibrium, so there are two nonidentical ground states from which excitation can occur. Two triplet excited states that do not readily interconvert are derived from the s-E and s-Z conformers. Theoretical calculations suggest that at their energy minimum the excited states of conjugated dienes can be described as an alkyl radical and an orthogonal allyl system called an allylmethylene diradical ... [Pg.772]

PCSs are systems of chromophores bound into a single macromolecule. Therefore, the study of processes of electronic excitation and energy transfer, as well as the investigation of the ways of deactivation of excited states, should lay a foundation for the understanding of such properties of PCSs as reactivity in photochemical transformations, photosensitizing and photoelectric activity, photoinitiated paramagnetism, etc. [Pg.22]

In the two most important types of photosensitization, both of which are in accord with the Wigner rule, a triplet excited state generates another triplet and a singlet generates a singlet ... [Pg.317]

Run/Nin heteronuclear complexes such as (653), in which a photosensitizer [Ru(bpy)3]2+ or [Ru(phen)3]2+ is covalently attached to the Ni1 cyclam complex, have been synthesized in order to improve the efficiency of electron transfer from the photoexcited photosensitizer to the catalytic site.1 44-1646 However, these complexes did not perform particularly well, either due to unfavorable configuration of the Nin-cyclam subunit and the resulting steric hindrance or due to short lifetime of the excited states of the Ru photosensitizer moieties. A stable catalytic system has been prepared by immobilizing macrocyclic Ni11 complexes and [Ru(bipy)3]2+ in a nafion membrane.164... [Pg.399]

In addition, the results indicated that the efficiency of cis —> trans increased as the initial cis double bond configuration is shifted from the center of the polyenic chain, consistent with the 7j, triplet excited state potential curve that has a very shallow minimum at the 15-cis position compared to the deep minima at the all-trans position. The results strongly suggest that isomerization takes place via the 7j state of the carotenoid even in the case of direct photoexcitation, with their photosensitized process because of the very low intersystem crossing quantum yield, isc ([Pg.246]

Moreover, carotenoids may quench electronically excited states and scavenge free radicals formed in the retina, and therefore protect biomolecules from oxidative damage. Due to the low energy level of the first excited triplet state ( Car), carotenoids (Car) can act as efficient acceptors of triplet state energy from photosensitizers (S) (Equation 15.1), such as all-tra .s-retinal, the photosensitizers of lipofuscin (Rozanowska et al., 1998), or singlet oxygen C02) (Equation 15.2) (Cantrell et al., 2003) ... [Pg.313]

The type I mechanism is a radical process, and involves the excited state of the photosensitizer in electron-transfer processes, as indicated in Scheme 1. The reactions there are essentially photochemically stimulated autoxidation processes. [Pg.948]

Stiel, H., Teuchner, K., Paul, A., Leupold, D. and Kochevar, I. E. (1996). Quantitative comparison of excited state properties and intensity- dependent photosensitization by rose bengal. J. Photoch. Photobiol. B 33, 245-54. [Pg.142]


See other pages where Excited states photosensitization is mentioned: [Pg.235]    [Pg.18]    [Pg.137]    [Pg.5595]    [Pg.5596]    [Pg.1286]    [Pg.235]    [Pg.18]    [Pg.137]    [Pg.5595]    [Pg.5596]    [Pg.1286]    [Pg.428]    [Pg.436]    [Pg.776]    [Pg.60]    [Pg.77]    [Pg.316]    [Pg.317]    [Pg.11]    [Pg.186]    [Pg.176]    [Pg.250]    [Pg.239]    [Pg.247]    [Pg.249]    [Pg.312]    [Pg.326]    [Pg.357]    [Pg.340]    [Pg.466]    [Pg.745]    [Pg.962]    [Pg.973]    [Pg.975]    [Pg.110]    [Pg.206]    [Pg.297]    [Pg.98]    [Pg.54]    [Pg.111]    [Pg.241]    [Pg.82]    [Pg.157]    [Pg.480]   
See also in sourсe #XX -- [ Pg.340 , Pg.341 ]




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