Dimerization photochemical

Dihydrodithiin sulphoxides, synthesis of 243 Dihydrothiophene dioxides, reactions of 653 /(,/( -Dihydroxyketones 619 Dimerization, photochemical 877, 884 Dimethyl sulphoxide anion of - see Dimsyl anion hydrogen bonding with alcohols and phenols 546-552 oxidation of 981, 988 photolysis of 873, 874, 988 radiolysis of 890-909, 1054, 1055 self-association of 544-546 Dimsyl anion... 

Alkvnes do rot dimerize photochemically to give cyclobutadienes, but dimers are formed from arylalkynes under conditions of electron-transfer sensitization (2.105). These dimers arise from a reaction of the alkyne radical cation with ground-slate alkyne, followed by intramolecular electrophilic attack on the benzene ring. 

There are two different methods of splitting a thymine dimer photochemical and enzymatic. In the photochemical method, the sample containing thymine dimers is irradiated with UV light. Splitting of the thymine cyclobutane dimer follows the same symmetry rules as its formation it is thermally forbidden but photochemically allowed. When a dimer absorbs a photon of suitable wavelength (2 240 nm), it reacts with a quantum yield of nearly 100% forming two thymines [60]. In the enzymatic method an enzyme recognizes thymine dimers and repairs them. It may require the absorption of a photon, or it may happen in the dark. 

Alkenes can be dimerized photochemically in this way, but reaction between two different alkenes is more interesting. If one alkene is bonded to a conjugating group, it alone will absorb UV light and... 

Alkenes can be dimerized photochemically in this way, but reaction between two different alkenes is more interesting, if one alkene is bonded to a conjugating group, it alone will absorb UV light and be excited while the other will remain in the ground state. It is difficult to draw a mechanism for these reactions as we have no simple way to represent the excited alkene. Some people draw it as a diradical (since each electron is in a different orbital) others prefer to write a concerted reaction on an excited alkene marked with an asterisk. 

Andr asson J, Kyrychenko A, MMensson J and Albinsson B. Temperature and Viscosity Dependence of the Triplet Energy Transfer Process in Porphyrin Dimers. Photochem. Photobiol. Sci. 2002 1 111-119. 

Additional work showed that the dimerization of arylazirines to 1,3-diazabicy-clo[3.1.0]hex-3-enes is a general reaction which is independent of the nature of the substituent groups attached to the C atom of the azirine ring. Care is required in the choice of solvent, photolysis time and substituents since the 1,3-diazabicyclohexenes are themselves photochemically labile (72JA7788). 

A peculiar case of fast and reversible (i.e., tautomeric) isomerizations initiated thermally or photochemically is represented by triarylimidazole dimers 349a formed by oxidation of triaryUmidazoles (66JA3825 90MI2) and diarylhetarylimidazoles (Ar = Het) (Scheme 140) [97MI553]. 

Photochemical reaction of the ester 114 afforded the alkene 115 and three products derived from 115. A mechanism, involving dimerization of 114 leading to a dithietane intermediate 116, was proposed. Trapping of active sulfur species, generated from 116, with dienes was also described (75CB630). 

Tile following photochemical conversions also involve 1,2-dithietes as intermediates whose chemical trapping was reported in most cases. Tlie formation of the dithiin 249 from 250 may best be explained by the formation of the dithiete dimer 251 and the loss of S2 (73ZC424).Tlie formation of 252 and 253 from 254 (78NJC331) should be compared with the sulfuration of the acetylene 182 with elemental sulfur (93BCJ623).Tlie photolysis of 255 provides a rare example when the ejection of a nitrile was employed for the generation of a 1,2-dithiete (73ZC431). 

UV irradiation. Indeed, thermal reaction of 1-phenyl-3,4-dimethylphosphole with (C5HloNH)Mo(CO)4 leads to 155 (M = Mo) and not to 154 (M = Mo, R = Ph). Complex 155 (M = Mo) converts into 154 (M = Mo, R = Ph) under UV irradiation. This route was confirmed by a photochemical reaction between 3,4-dimethyl-l-phenylphosphole and Mo(CO)6 when both 146 (M = Mo, R = Ph, R = R = H, R = R" = Me) and 155 (M = Mo) resulted (89IC4536). In excess phosphole, the product was 156. A similar chromium complex is known [82JCS(CC)667]. Complex 146 (M = Mo, R = Ph, r2 = R = H, R = R = Me) enters [4 -H 2] Diels-Alder cycloaddition with diphenylvinylphosphine to give 157. However, from the viewpoint of Woodward-Hoffmann rules and on the basis of the study of UV irradiation of 1,2,5-trimethylphosphole, it is highly probable that [2 - - 2] dimers are the initial products of dimerization, and [4 - - 2] dimers are the final results of thermally allowed intramolecular rearrangement of [2 - - 2] dimers. This hypothesis was confirmed by the data obtained from the reaction of 1-phenylphosphole with molybdenum hexacarbonyl under UV irradiation the head-to-tail structure of the complex 158. 

Pyrolyses of Nl- or N3-substituted derivatives of compounds 4 and 5 have continued to find use as routes to azacarbazoles, although the yields are often indifferent and there are no recent examples. The photochemical reactions are dealt with in Section IV.G. Pyrolysis media are paraffin (P) or PPA, and examples of products are compounds 247 (P, cytostatic) (83MI2), 248 (P) (84MI1), and 249 (from a 1-substituted derivative) (86MI2). Indications of diradical intermediates are provided by the thermolysis of compound 250 (P) (83MI2) where one product is a dimer. 

Phenylbenzisothiazolescan be photochemically transformed to benzophenone derivatives however. depending on the solvent, 1,5-diazocine systems, generated by dimerization of the primarily formed product, can be isolated.36... 

The activation of silylene complexes is induced both photochemically or by addition of a base, e.g. pyridine. A similar base-induced cleavage is known from the chemistry of carbene complexes however, in this case the carbenes so formed dimerize to give alkenes. Finally, a silylene cleavage can also be achieved thermally. Melting of the compounds 4-7 in high vacuum yields the dimeric complexes 48-51 with loss of HMPA. The dimers, on the other hand, can be transformed into polysilanes and iron carbonyl clusters above 120 °C. In all cases, the resulting polymers have been identified by spectroscopic methods. 

Photochemical disproportionation of metal-metal bonded carbonyl dimers. A. E. Stiegman and D. R. Tyler, Coord. Chem. Rev., 1985, 63, 217 (59). 

The syntheses of perhalogenated dithiethanes and their oxidation products (214-219) have been recently reported247. The method is based on the photochemical dimerization of thiophosgen or its fluoro- and bromo-analogues followed by partial oxidation with trifluoroperacetic acid to the desired sulfoxides (or sulfones)248 as shown in equation 84. 

Different dianhydrides have been syndiesized or are commercially available, and some structures arc shown in Fig. 5.9.64-66 An improved method for preparation of cyclobutanetetracarboxylic dianhydride (CBDA) by photochemical dimerization of die maleic anhydride has been developed by Nissan.67 The polyimide obtained by condensation of CBDA widi oxydianiline gives a transparent and colorless material. The transmittance of 50-pm-thick film is 82% and the UV cutoff is 310 nm. 

It is evident from the nature of the products, especially those formed with toluene present, that the photoreaction in weakly acidic medium involves incursion of a radical species. The complete suppression of reactions leading to the above products, in the presence of oxygen, strongly suggests that it is an excited triplet trityl ion which undergoes reaction. It is postulated that the primary photochemical process is the abstraction of a hydrogen atom by the triplet trityl ion to form the radical cation 90, which was proposed as an intermediate in the dimerization reactions carried out in strong acid (Cole, 1970). 

Co2(CO)8 has also been studied in low-temperature matrices (19,20), the photochemical behavior of which led to the identification of three isomeric forms of the dimer complex (19). Two of these are the accepted forms, 1 and 2, whereas the third has no bridging, CO ligands. The structure most... 

Photochemical 2 + 2 cycloadditions can also take place intramolecularly if a molecule has two double bonds that are properly oriented. " The cyclization of the quinone dimer shown above is one example. Other examples are... 

It is possible that some of these photochemical cycloadditions take place by a lA + A] mechanism, which is of course allowed by orbital symmetry when and if they do, one of the molecules must be in the excited singlet state (5i) and the other in the ground state.The nonphotosensitized dimerizations of cis- and trans-2-butene are stereospecific,making it likely that the [n2s + n2s] mechanism is operating in these reactions. However, in most cases it is a triplet excited state that reacts with the ground-state molecule in these cases the diradical (or in certain... 

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