108088-84-2Relevant academic research and scientific papers
Photochemical nitration by tetranitromethane. Part XXVII. Adduct formation in the photochemical reaction of 4-methylanisole. Solvent and temperature effects on the regiochemistry of reaction of the radical cation of 4-methylanisole
Butts, Craig P.,Eberson, Lennart,Hartshorn, Michael P.,Robinson, Ward T.
, p. 122 - 131 (2007/10/03)
The photolysis of the charge-transfer complex of 4-methylanisole and tetranitroroethane in dichloromethane gives four isomcnc nitro-triniromethyl adducts, including the epimeric 1-methoxy-4-methyl-3-nitro-6-trinitromethylcyclohexa-1,4-dienes 3 and 4 and the epimeric 1-methoxy-4-methyl-6-nitro-3-trinitromethylcyclohexa-1,4-dienes 5 and 6, 4-methyl-2-trinitromethylanisole 1, 4-methyl-2-nitroanisole 2, nitrophenols 7 and 9, and 4-methyl-4-nitrocyclohexa-2,5-dienone 8. Similar reaction in acetonitrile also gives these products, with the exception of two of the adducts (3 and 4). The effect of reaction temperature on the yields of the various products indicates that they are formed either by attack of trinrtromethanide ion on the radical cation of 4-methylanisole vicinal to the methoxy group at C2 (1, 3 and 4), or by attack of trinitromethanide ipso to the methoxy group (2, 5, 6 and 8). By conducting the photolysis in dichloromethane with trifluoroacetic acid present, the trinitromethanide pathway is eliminated, and the products formed are derived from reaction between 4-methylanisole and or its radical cation and NO2. The effects of added salts Bu4N+ClO4- (TBAP) or Bu4N+C(NO2)3- (TBAT) to reactions on dichloromethane are seen as the consequences of changes in the polarity of the solvent and not to competition between ion-pair and radical-pair collapse during the reactions. By analogy with adducts 3 and 4, two adducts 16 and 17 derived from similar photolysis reactions of 4-chloroanisole are shown to be the epimeric 4-chloro-1-methoxy-3-nitro-6-trinitromethyleyclohexa-1,4-dienes It and 17 rather than nitrit(or hydroxy)-trinitromethyl adducts. The X-ray crystal Structure of 1-methoxy-4-methyl-r-3-nitro-c-6-trinitromethylcyclohexa-1,4-. diene 3 is reported. Acta Chemica Scandinavica 1996.
I. Photochemical nitration of methoxybenzenes from charge-transfer complexes with tetranitromethane
Sankararaman, S.,Kochi, J. K.
, p. 278 - 285 (2007/10/02)
The direct irradiation of the charge-transfer (CT) absorption band of the 1/1 electron donor-acceptor complexes of dimethoxybenzenes with tetranitromethane leads to aromatic nitration with a high quantum yield.The analogous methoxytoluenes under the same photochemical conditions are converted in equally high yields to products of aromatic trinitromethylation.This dichotomy with different methoxybenzenes (ArH) is discussed within the context of the common reactive intermediates derived from the CT excitation of the complex.The subsequent interactions of the geminate fragments, i.e., +., C(NO2)3-, .NO2>, by radical-pair and ion-pair annihilation represent a unifying mechanism for the CT photochemistry leading to aromatic nitration and trinitromethylation.
