http://www.cnr.it/ontology/cnr/individuo/prodotto/ID50665
Primary Photoinduced Processes in Bimetallic Dyads with Extended Aromatic Bridges. Tetraazatetrapyridopentacene Complexes of Ruthenium(II) and Osmium(II). (Articolo in rivista)
- Type
- Label
- Primary Photoinduced Processes in Bimetallic Dyads with Extended Aromatic Bridges. Tetraazatetrapyridopentacene Complexes of Ruthenium(II) and Osmium(II). (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ic051062z (literal)
- Alternative label
C. Chiorboli, S. Fracasso, M. Ravaglia, F. Scandola, S. Campagna, K. L. Wouters, R. Konduri, and F. M. MacDonnell (2005)
Primary Photoinduced Processes in Bimetallic Dyads with Extended Aromatic Bridges. Tetraazatetrapyridopentacene Complexes of Ruthenium(II) and Osmium(II).
in Inorganic chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- C. Chiorboli, S. Fracasso, M. Ravaglia, F. Scandola, S. Campagna, K. L. Wouters, R. Konduri, and F. M. MacDonnell (literal)
- Pagina inizio
- Pagina fine
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- Rivista
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- ISOF-CNR, Sezione di Ferrara, 44100 Ferrara, Italy, Dipartimento di Chimica, UniVersita` di
Ferrara, and INSTM, Sezione di Ferrara 44100 Ferrara, Italy, Dipartimento di Chimica
Inorganica, Chimica Analitica e Chimica Fisica, UniVersita` di Messina, and INSTM, Sezione di
Messina, 98166 Messina, Italy, and Department of Chemistry and Biochemistry, The UniVersity of
Texas at Arlington, Arlington, Texas 76019 (literal)
- Titolo
- Primary Photoinduced Processes in Bimetallic Dyads with Extended Aromatic Bridges. Tetraazatetrapyridopentacene Complexes of Ruthenium(II) and Osmium(II). (literal)
- Abstract
- The photophysics of the binuclear complexes [(phen)2M(tatpp)M(phen)2]4+, where M ) Ru or Os, phen ) 1,10-
phenanthroline, and tatpp ) 9,11,20,22-tetraazatetrapyrido[3,2-a:2¢3¢-c:3¢¢,2¢¢-l:2¢¢¢,3¢¢¢]pentacene, has been studied
in acetonitrile and dichloromethane by femtosecond and nanosecond time-resolved techniques. The results
demonstrate that complexes of different metals have different types of lowest excited state: a tatpp ligand-centered
(LC) triplet in the case of Ru(II); a metal-to-ligand charge-transfer (MLCT) triplet state in the case of Os(II). The
excited-state kinetics is strongly solvent-dependent. In the Ru(II) system, the formation and decay of the LC state
take place, respectively, in 25 ps and ca. 5 ns in CH3CN and in 0.5 ps and 1.3 ís in CH2Cl2. These solvent effects
can be rationalized on the basis of a thermally activated decay of the LC state through the upper MLCT state. In
the Os(II) system, the formation and decay of the MLCT state take place, respectively, in 3.8 and 60 ps in CH3CN
and in 0.5 and 4 ps in CH2Cl2. These effects are consistent with the solvent sensitivity of the MLCT energy, in
terms of driving force and energy-gap law arguments. The relevance of these results for the use of ladder-type
aromatic bridges as potential molecular wires is discussed. (literal)
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- Autore CNR
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