A novel chemiluminescence from the reaction of 9-arylmethylene-10-methyl-9,10-dihydroacridines and peroxyacid
摘要:
Reaction of 9-arylmethylene-10-methyl-9,10-dihydroacridine (1) with more than two equivalents of m-choloroperoxybenzoic acid in CH2Cl2 affords intermediary beta-hydroxy-tertiary-alkyl peroxyester (5) decomposing to N-methylacridone and aromatic aldehyde with chemiluminescence by a CIEEL mechanism.
Reaction of 9-arylmethylene-10-methyl-9,10-dihydroacridine (1) with isolated dimethyldioxirane affords cleavage products with chemiluminescence via a 1,2,4-trioxan (5) which will be formed by the reaction of an intermediary epoxide (3) with dimethyldioxirane as nucleophile.
Sakanishi Katsumasa, Kato Yoshiyuki, Mizukoshi Emi, Shimizu Kazufumi, Tetrahedron Lett, 35 (1994) N 27, S 4789-4792
Reaction of 9-arylmethylene-10-methyl-9,10-dihydroacridine (1) with more than two equivalents of m-choloroperoxybenzoic acid in CH2Cl2 affords intermediary beta-hydroxy-tertiary-alkyl peroxyester (5) decomposing to N-methylacridone and aromatic aldehyde with chemiluminescence by a CIEEL mechanism.