Reaction mechanisms intersystem crossing

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). 

Fig. 1 Schematic mechanism for the long-distance oxidation of DNA. Irradiation of the anthraquinone (AQ) and intersystem crossing (ISC) forms the triplet excited state (AQ 3), which is the species that accepts an electron from a DNA base (B) and leads to products. Electron transfer to the singlet excited state of the anthraquinone (AQ 1) leads only to back electron transfer. The anthraquinone radical anion (AQ ) formed in the electron transfer reaction is consumed by reaction with oxygen, which is reduced to superoxide. This process leaves a base radical cation (B+-, a hole ) in the DNA with no partner for annihilation, which provides time for it to hop through the DNA until it is trapped by water (usually at a GG step) to form a product, 7,8-dihydro-8-oxoguanine (8-OxoG)...

A recently popular mechanism involves the intersystem crossing of the cis- or trons-stilbene singlet state, produced upon direct photolysis, to its corresponding triplet states, which would then undergo the type of reactions given in Eqs. (9.8M9.10) and (9.17M9.19) ... 

Notice that this is the same as the mechanism written in Section II except that step (9), self-quenching, has been added. If we assume that the quantum yield of intersystem crossing for the sensitizer is unity and that all the sensitizer triplet is quenched either by the acceptor or by ground state sensitizer, then the following expression for 4>a, the actual quantum yield for reaction of the substrate triplet, can be derived ... 

For the reactions described so far in this section, the ketone substrates have lowest excited states that are (n.ii ) in character aliphatic ketones may react by way of the singlet or the triplet state, and aryl ketones normally through the triplet because intersystem crossing is very efficient. The efficiency of photochemical hydrogen abstraction from compounds such as alcohols or ethers is very much lower if the ketone has a lowest (Ji,n triplet state, as does I - or 2-acetylnaphthalene (CmH-COMe). However, all aryl ketones, regardless of whether their lowest triplet state is fn,Jt l or (Jt.Ji ), react photochemically with amines to give photoreduction or photoaddition products. A different mechanism operates (4.38), that begins... 

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