http://www.cnr.it/ontology/cnr/individuo/prodotto/ID51236
Fullerene Derivatives Functionalized with Diethylamino-Substituted Conjugated Oligomers: Synthesis and Photoinduced Electron Transfe (Articolo in rivista)
- Type
- Label
- Fullerene Derivatives Functionalized with Diethylamino-Substituted Conjugated Oligomers: Synthesis and Photoinduced Electron Transfe (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/chem.200901216 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- A. Gégout; J.-F. Nierengarten; B. Delavaux-Nicot; C. Duhayon; A. Saquet; A. Listorti; A. Belbakra;, C. Chiorboli; N. Armaroli (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Laboratoire de Chimie des Mat?riaux Mol?culaires
Universit? de Strasbourg et CNRS (UMR 7509)
Ecole Europ?enne de Chimie, Polym?res et Mat?riaux (ECPM)
25 rue Becquerel, 67087 Strasbourg Cedex 2 (France)
Laboratoire de Chimie de Coordination du CNRS
205 route de Narbonne, 31077 Toulouse Cedex 4 (France)
Molecular Photoscience Group Istituto per la Sintesi Organica e la Fotoreattivit?
Istituto per la Sintesi Organica e la Fotoreattivit?à
Consiglio Nazionale delle Ricerche
via Gobetti 101, 40129 Bologna (Italy)
Istituto per la Sintesi Organica e la Fotoreattivit?à
Consiglio Nazionale delle Ricerche, Sezione di Ferrara
via Borsari 46, 44100 Ferrara (Italy) (literal)
- Titolo
- Fullerene Derivatives Functionalized with Diethylamino-Substituted Conjugated Oligomers: Synthesis and Photoinduced Electron Transfe (literal)
- Abstract
- Abstract: Diethylamino-substituted oligophenylenevinylene
(OPV) building
blocks have been prepared and used
for the synthesis of two [60]fullerene-
OPV dyads, F-D1 and F-D2, which exhibit
different conjugation length of
the OPV fragments. The electrochemical
properties of these acceptor-donor
dyads have been studied by cyclic voltammetry.
The first reduction is always
assigned to the fullerene moiety and
the first oxidation centered on the diethylaniline
groups of the OPV rods,
thus making these systems suitable candidates
for photoinduced electron
transfer. Both the OPV and the fullerene-
centered fluorescence bands are
quenched in toluene and benzonitrile,
which suggests the occurrence of photoinduced
electron transfer from the
amino-substituted OPVs to the carbon
sphere in the dyads in both solvents.
By means of bimolecular quenching experiments,
transient absorption spectral
fingerprints of the radical cationic species
are detected in the visible
(670 nm) and near-IR (1300-1500 nm)
regions, along with the much weaker
fullerene anion band at lmax=1030 nm.
Definitive evidence for photoinduced
electron transfer in F-D1 and F-D2
comes from transient absorption measurements.
A charge-separated state is
formed within 100 ps and decays in less
than 5 ns. (literal)
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