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A fully self-assembled non-symmetric triad for photoinduced charge separation (Articolo in rivista)
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- A fully self-assembled non-symmetric triad for photoinduced charge separation (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c0sc00520g (literal)
- Alternative label
Iengo, E (Iengo, Elisabetta); Pantos, GD (Pantos, G. Dan); Sanders, JKM (Sanders, Jeremy K. M.); Orlandi, M (Orlandi, Michele); Chiorboli, C (Chiorboli, Claudio); Fracasso, S (Fracasso, Sandro); Scandola, F (Scandola, Franco) (2011)
A fully self-assembled non-symmetric triad for photoinduced charge separation
in Chemical science (Camb. 2010. Online); ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE,, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND (Regno Unito)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Iengo, E (Iengo, Elisabetta); Pantos, GD (Pantos, G. Dan); Sanders, JKM (Sanders, Jeremy K. M.); Orlandi, M (Orlandi, Michele); Chiorboli, C (Chiorboli, Claudio); Fracasso, S (Fracasso, Sandro); Scandola, F (Scandola, Franco) (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Univ Cambridge, Chem Labs, Cambridge CB2 1EW, England
Univ Trieste, Dipartimento Sci Chim & Farmaceut, I-34127 Trieste, Italy
Univ Ferrara, Dipartimento Chim, I-44100 Ferrara, Italy
ISOF CNR, Sez Ferrara, I-44100 Ferrara, Italy (literal)
- Titolo
- A fully self-assembled non-symmetric triad for photoinduced charge separation (literal)
- Abstract
- A very efficient and successful metal-mediated strategy towards the formation of a non-symmetric triad is described: appropriate Lewis acid and/or base functions on the molecular components (a naphthalenediimide, an aluminium(III) porphyrin, and a ruthenium(II) porphyrin) lead to the desired product uniquely. The photophysics of the triad was investigated in detail using time-resolved spectroscopy in the pico- and nanosecond time domains. The strategy is of great potential interest as, while confining the synthetic effort to the single components, it can give access to a wide range of photoactive systems (literal)
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