Synthesis and transformation of a novel methano[60]fullerene having a formyl group
摘要:
The reaction of [60]fullerene with a dimethylsulfonium alpha -formylalkylide gave a novel methano[60]fullerene having a formyl group at the bridge-head carbon, This 2.2-[60]fulleroalkanal was readily converted into a variety of N-aryl-2,2-[60]fulleroaldimines by condensation with aromatic amines: one of them showed efficient quenching of the fluorescence of the [60]fullerene core, due to a photoinduced intramolecular electron transfer. (C) 2001 Elsevier Science Ltd. All rights reserved.
Synthesis and transformation of a novel methano[60]fullerene having a formyl group
摘要:
The reaction of [60]fullerene with a dimethylsulfonium alpha -formylalkylide gave a novel methano[60]fullerene having a formyl group at the bridge-head carbon, This 2.2-[60]fulleroalkanal was readily converted into a variety of N-aryl-2,2-[60]fulleroaldimines by condensation with aromatic amines: one of them showed efficient quenching of the fluorescence of the [60]fullerene core, due to a photoinduced intramolecular electron transfer. (C) 2001 Elsevier Science Ltd. All rights reserved.
It was found that various kinds of α-substituted carbonyl-stabilized sulfoniumylides were conveniently prepared from the corresponding sulfonium salts by treating with 50% aqueous sodium hydroxide. The reactions of sulfoniumylides with succinic anhydride afforded furofuran derivative by one step procedure in yields ranging these from 5 to 14%. The structures of furofuran derivatives were confirmed