Triplet state sensitizer

Rodgers, M.A.J. and Bates A.L. 1980. Kinetic and spectroscopic features of some carotenoid triplet states Sensitization by singlet oxygen. Photochem. Photobiol. 31 533-537. 

Figure 4.34 Photoelimination reactions of nitrogen, (a) Formation of a carbene through triplet state sensitization, and addition of molecular oxygen, (b) Formation of nitrenes through photodissociation of azo compounds and azides...

In type I photosensitized oxidation, the triplet state sensitizer abstracts a hydrogen or electron from the unsaturated oil, producing radicals that initiate chain propagation as in autoxidation. However, chain-breaking antioxidants do not stop this reaction as new radicals are produced photochemically. In type II photooxidation, the energy of the triplet sensitizer is transferred to molecular oxygen, converting it... 

Photochemical fatigue of 6-nitro-BIPS (6) depended on the presence in solution of triplet sensitizers or quenchers. The triplet energy Er for 6 is 64.3 kcal mol-1. When benzophenone, a triplet-state sensitizer having a triplet energy Er— 69.2 kcal mol -was added to solutions of 6, a considerable acceleration of the fatigue was observed (Figure 14). On the other hand, 1,1 -binaphthyl ( >=54.3 kcal mol-1) acted as a triplet-state quencher, and its presence in solution decreased the colorability (Figure 15). 

As an introduction, the mechanism responsible for the outdoor photooxidative degradation of many synthetic polymers can be summarized in Figure 29 (110,111). Some absorbing chromophore absorbs sunlight to produce an excited electronic state, which may, in addition to the usual physical fates, suffer chemical reactions leading ultimately to loss of mechanical properties of the polymer. Such reactions Include direct molecular dissociation, such as the Norrlsh Type II process referred to earlier (see Section II), production of O2 ( g) generally through triplet-state sensitization... 

The enhancement of the curing rate by additions of thioxanthone was studied with time-resolved laser spectroscopy and H-NMR CIDNP. It led to the conclusion that two competitive processes occur from the excited triplet-state sensitizers. One is electron transfer and the other is enei transfer. Whether it is the former or the latter depends upon the structure of the initiator used. ... 

A principal appHcation for photomedicine is the photodynamic treatment of cancer. Photochemical and clinical aspects of this topic have been reviewed (10,11). Direct irradiation of tumors coupled with adininistration of a sensitizer is used to effect necrosis of the malignancy. In this process, an excited state sensitizer interacts with dissolved in vivo to effect conversion of the oxygen from its triplet ground state to an excited singlet state, which is highly cytotoxic. In principle, excited sensitizers in either the singlet or the triplet state can effect this conversion of molecular oxygen (8). In... 

Commercially, the irradiation of the 5,7-diene provitamin to make vitamin D must be performed under conditions that optimize the production of the previtamin while avoiding the development of the unwated isomers. The optimization is achieved by controlling the extent of irradiation, as well as the wavelength of the light source. The best frequency for the irradiation to form previtamin is 295 nm (64—66). The unwanted conversion of previtamin to tachysterol is favored when 254 nm light is used. Sensitized irradiation, eg, with fluorenone, has been used to favor the reverse, triplet-state conversion of tachysterol to previtamin D (73,74). 

The energy of the triplet state of the sensitizer ( Sens ) must be greater than that of the reactant. If this condition is not met, the energy transfer becomes endothermic and cannot compete with other transformations of Sens. ... 

The transfer of energy must proceed with net conservation of spin. In the usual case, the acceptor molecule is a ground-state singlet, and its reaction with the triplet state of the sensitizer will produce the triplet state of the acceptor. The mechanism for triplet photosensitization is outlined below ... 

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... 

A which is not observed in individual solutions of the two enones at the same concentrations and may thus be indicative of a complex formation. However, the ratio of isomeric cyclobutane products resulting from such photocycloadditions is generally seen to be a quite sensitive function of steric effects and of the properties of the reaction solvent, of the excited state(s) involved (in some cases two different excited triplet states of the same enone have been found to lead to different adducts) and of the substituents of the excited enone and substrate. No fully satisfactory theory has yet been put forth to draw together all the observations reported thus far. 

The sensitized reaction on furan led to the formation of a triplet state of 1 then the relaxation of O—Cq, bonds can induce, by crossing onto a energy sheet, the formation of a tt,(j biradical 9 (74JA3486 76T1729 99MI1). 

Semiempirical (PM3) and ab initio (6-3IG basis set) calculations are in agreement with the hypothesis described in Section I (99MI233 OOOJOC2494). In the case of the sensitized reaction, when the excited triplet state is populated, only the formation of the radical intermediate is allowed. This intermediate can evolve to the corresponding cyclopropenyl derivative or to the decomposition products. In a previously reported mechanism the decomposition products resulted from the excited cyclopropenyl derivative. In our hypothesis the formation of both the decomposition products and the cyclopropenyl derivatives can be considered as competitive reactions. 

Also in this case the relative energy of all the possible intermediates involved in the photochemical isomerization was calculated (OOOJOC2494). The results are collected in Fig. 2. Also in this case the sensitized irradiation involves the formation of the biradicals. We have to note, however, that the fission of O—Cq, bond in the triplet state of the molecule is not so favored as in furan. The process should be quite inefficient. The corresponding biradicals show the same energy as that in the triplet state. In this case, then, the formation of a biradical should depend on the activation energy. 

Compound 104 could not be obtained from 103, and a hypothesis about its formation considered the (homolytic or heterolytic) cleavage of the O—N bond (Scheme 43) (68TL2417). The sensitized reaction didnotgive adifferentresult the author supposed that the reaction involved the excited triplet state of the molecule. When the reaction was carried out in methanol, 104 was obtained in 8% yield... 

The results described above represent the first example of the FR mechanism (Scheme 1). Semiempirical calculations on this molecule showed that the intersystem crossing to the excited triplet state is favored The reaction cannot be sensitized by xanthone because the triplet state of 3,4-diphenyl-1,2,5-oxadiazole is lower than that of xanthone. The cleavage of the triplet state to the biradical is favored, considering the relative energy of this intermediate (Fig. 23) (OOOUPl). 

Quenching of the Intersystem Crossing to the Triplet State 521 Photoinduced 1RAV Studies 522 Time-Resolved Photoinduced Studies 524 Sensitization of Photoconductivity 525 Magnetic Properties 526... 

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