http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48184
Heteroaromatic Donor-Acceptor pi-Conjugated 2,2 '-Bipyridines (Articolo in rivista)
- Type
- Label
- Heteroaromatic Donor-Acceptor pi-Conjugated 2,2 '-Bipyridines (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Alternative label
Abbotto, A.; Bellotto, L.; De Angelis, F.; Manfredi, N.; Marinzi, C. (2008)
Heteroaromatic Donor-Acceptor pi-Conjugated 2,2 '-Bipyridines
in European journal of organic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Abbotto, A.; Bellotto, L.; De Angelis, F.; Manfredi, N.; Marinzi, C. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- DOI: 10.1002/ejoc.200800692 (literal)
- Note
- ISI Web of Science (WOS) (literal)
- Titolo
- Heteroaromatic Donor-Acceptor pi-Conjugated 2,2 '-Bipyridines (literal)
- Abstract
- A series of heteroaromatic 4,4'-pi-conjugated 2,2'-bipyridines (bpy)
bearing conjugated pi-excessive and pi-deficient heteroaromatic rings
as donor (D) and acceptor (A) substituents, respectively, is presented.
We have experimentally and computationally found that, upon variation
of donor and acceptor properties of the heterocyclic subunits in
combination with different structural symmetries (bpy-pi-D or
bpy-pi-D-pi-A), the absorption and emission maxima and molecular
orbital energy levels can be easily tuned over a broad range.
Properties of the new ligands can be efficiently exploited in metal
complexes for dye-sensitized solar cells and in other materials for
optical applications. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451
Weinheim, Germany, 2008) (literal)
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- Autore CNR
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