Open-[60]fullerene-aniline conjugates with near-infrared absorption.

ABSTRACT: Two open-[60]fullerene-aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS₂. By increasing the number of N,N-dimethylaniline moieties, the absorption edge was considerably shifted up to 1200 nm owing to effective acceptor-donor interactions.

SUBMITTER: Sadai S 

PROVIDER: S-EPMC10177950 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature