
%0 Journal Article
%A Calvert, JL 
%A Eberson, L 
%A Hartshorn, MP 
%A Maclaga, n 
%A Robinson, WT 
%T Photochemical Nitration by Tetranitromethane. XVII. The Regiochemistry of Adduct Formation in the Photochemical Reaction of 1-Methylnaphthalene and Tetranitromethane
%J Australian Journal of Chemistry
%D 1994/08/01
%V 47
%N 8
%P 1591-1604
%K 
%R https://doi.org/10.1071/CH9941591
%U https://www.publish.csiro.au/paper/CH9941591 
%X Photolysis of the 1-methylnaphthalene/tetranitromethane charge-transfer complex yields the triad of 1-methylnaphthalene radical cation, nitrogen dioxide and trinitromethanide ion. Recombination of this triad gives predominantly 4-methyl-t-2-nitro-r-1-trinitromethyl-1,2- dihydronaphthalene (1), the epimeric 1-methyl-1-nitro-4-trinitromethyl-1,4-dihydronaphtha-lenes (2) and (3), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (4), nitro cyclo -adduct (5), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (6), hydroxy cyclo-adduct (7) and 4-methyl-t-1-trinitromethyl-1,2-dihydronaphthalen-r-2-ol (8). Adducts (1)- (3), (5), (7) and (8) are formed by attack of the trinitromethanide ion at C4 of the 1-methylnaphthalene radical cation, while adducts (4) and (6) are formed by corresponding attack at C5. Adduct (1) undergoes thermal cycloaddition to give the nitro cycloadduct (5) and it is assumed that the hydroxy  cycloadduct (7) is formed in analogous manner from 4-methyl-t-1-trinitromethyl-1,2-dihydronaphthalen-r-2-ol (8). X-Ray crystal structure determinations are reported for adducts (1), (3)-(5) and (7). 
