Photoactivation ethers

Various enol silyl ethers and quinones lead to the vividly colored [D, A] complexes described above and the electron-transfer activation within such a donor/acceptor pair can be achieved either via photoexcitation of charge-transfer absorption band (as described in the nitration of ESE with TNM) or via selective photoirradiation of either the separate donor or acceptor.41 (The difference arising in the ion-pair dynamics from varied modes of photoactivation of donor/acceptor pairs will be discussed in detail in a later section.) Thus, actinic irradiation with /.exc > 380 nm of a solution of chloranil and the prototypical cyclohexanone ESE leads to a mixture of cyclohexenone and/or an adduct depending on the reaction conditions summarized in Scheme 5. 

Exploitation of time-resolved spectroscopy allows the direct observation of the reactive intermediates (i.e., ion-radical pair) involved in the oxidation of enol silyl ether (ESE) by photoactivated chloranil (3CA ), and their temporal evolution to the enone and adduct in the following way.41c Photoexcitation of chloranil (at lexc = 355 nm) produces excited chloranil triplet (3CA ) which is a powerful electron acceptor (EKelectron-rich enol silyl ethers (Em = 1.0-1.5 V versus SCE) to the ion-radical pair with unit quantum yield, both in dichloromethane and in acetonitrile (equation 20). 

Photoactivation reactions of compiexes Mg(L)+ , where L=an aicohoi or ether... 

Free-radical, radiation-curable systems generally consist of monomers, oligomers, photoactivators, other resins, and fillers or tackifiers. An ultraviolet source or electron-beam generator is used to cure the systems. As an illustration Stueben (37) describes a typical UV-cured PSA system containing acrylates and polyvinyl ether. McGinniss (38) discusses formulation design related to UV-curable systems. The cationic photoinitiators are shown in Fig. 1. 

In 2011, Popik and co-workers reported photochemical dehydration of 3-hydroxy-2-naphthalenemethanol (o-naphthoquinone precursor, NQMP, 79) derivatives to o-naphthoquinone methides (oNQMs, 80) [78, 79]. The in situ generated reactive intermediate oNQM underwent facile cycloaddition with vinyl ethers (81) to form photostable benzochromans (82) (Scheme 12). NQMP (79) has two major absorption bands at 275 nm (log s = 4.06) and 324 nm (log s — 3.70) thus it can be photoactivated with either low pressure mercury lamp (254 nm) or fluorescent tubes (300 and 350 nm). The quantum yield of the photoactivation was very high (< 300 = 0.17 0.02 for 79). The in situ generated oNQMs was quenched mostly by... 

Scheme 12 Photoactivation of NQMP to generate oNQM, which then reacts with vinyl (thio)ether...

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