Pregled bibliografske jedinice broj: 527294
Ultrafast photoinduced intramolecular charge transfer in push–pull distyryl furan and benzofuran: solvent and molecular structure effect
Ultrafast photoinduced intramolecular charge transfer in push–pull distyryl furan and benzofuran: solvent and molecular structure effect // Physical Chemistry Chemical Physics, 13 (2011), 10; 4519-4528 doi:10.1039/C0CP02337J (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 527294 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ultrafast photoinduced intramolecular charge transfer in push–pull distyryl furan and benzofuran: solvent and molecular structure effect
Autori
Carlotti, Benedetta ; Spalletti, Anna ; Šindler-Kulyk, Marija ; Elisei, Fausto
Izvornik
Physical Chemistry Chemical Physics (1463-9076) 13
(2011), 10;
4519-4528
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
push–pull distyryl furan; time-resolved transient absorption; fluorescence spectroscopies
Sažetak
The excited state deactivation pathways of push–pull distyryl furan and benzofuran derivatives in several organic solvents were investigated in detail by using time-resolved transient absorption and fluorescence spectroscopies, with nano- and femto-second time resolution. Solvent polarity was found to play a key role in determining the efficiencies of fluorescence, intersystem crossing and internal conversion. The triplet yield gradually decreased, while the internal conversion increased upon increasing the solvent dielectric constant. However the fluorescence showed a different solvent polarity effect in the low and high solvent polarity region, with a reversal of the trend of fluorescence properties (quantum yield and lifetime). This fact points to an emitting state of a different nature (smaller and larger dipole moments) in the two cases, as also suggested by the huge fluorosolvatochromism. In fact the ultrafast spectroscopic investigation evidenced the presence of two transients characterized by peculiar spectral shapes assigned to a locally excited (LE) and a charge transfer (CT) state. In the more polar solvents the CT state was the longer lived, fluorescent one and an intramolecular charge transfer process was found to be operative and to become faster (up to B200–250 fs) in the higher polarity media. On the contrary, distyrylfuran, which exhibits the same molecular skeleton without the push–pull character showed a similar excited state dynamics in solvents of different polarities.
Izvorni jezik
Engleski
Znanstvena područja
Fizika, Kemija
POVEZANOST RADA
Projekti:
125-0982933-2926 - Heteropolicikli, strukturne osnove za bioaktivne spojeve. Sinteza i fotokemija (Škorić, Irena, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Marija Šindler
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE