New π-extended tetrathiafulvalene-containing fulleropyrrolidine dyads endowed with vinyl spacers

• Published in: Journal of organometallic chemistry Vol. 599; no. 1; pp. 2 - 7
• Main Authors: Herranz, M.A, Martı́n, N, Sánchez, L, Seoane, C, Guldi, D.M
• Format: Journal Article
• Language: English
• Published: LAUSANNE Elsevier B.V 09.04.2000; Elsevier
• Subjects: Chemistry; Chemistry, Inorganic & Nuclear; Chemistry, Organic; Cyclic voltammetry; Donor–acceptor dyads; Electron transfer; Fluorescence; Fullerene; Physical Sciences; Science & Technology; π-Extended tetrathiafulvalenes; Fullerene; Cyclic voltammetry; π-Extended tetrathiafulvalenes; Fluorescence; Electron transfer; Donor–acceptor dyads; BIS-LINKING; DONOR; ANALOGS; REDOX PROPERTIES; FULLERENES; ELECTRON-TRANSFER; cyclic voltammetry; electron transfer; donor-acceptor dyads; fluorescence; pi-extended tetrathiafulvalenes; ORGANOFULLERENES; C-60; DERIVATIVES; fullerene

The synthesis of novel C 60-donor dyads in which the fulleropyrrolidine moiety is covalently attached to an π-extended tetrathiafulvalene analogue through an ethylenic spacer is described. The cyclic voltammetry confirms the redox reactivity of both donor and acceptor chromophores and the semiempiri...