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Pregled bibliografske jedinice broj: 827976

Deactivating effect of the pyridine n, π* states on the photoreactivity of 5-[2-(pyrid-n-yl)ethenyl]oxazole (n = 2, 3 and 4)


Botti, V.; Elisei, F.; Faraguna, Fabio; Marinić, Željko; Mazzucato, U.; Šagud, Ivana; Šindler-Kulyk, Marija; Spalletti, A.
Deactivating effect of the pyridine n, π* states on the photoreactivity of 5-[2-(pyrid-n-yl)ethenyl]oxazole (n = 2, 3 and 4) // Journal of photochemistry and photobiology. A, Chemistry, 329 (2016), 262-272 doi:10.1016/j.jphotochem.2016.07.009 (međunarodna recenzija, članak, znanstveni)


Naslov
Deactivating effect of the pyridine n, π* states on the photoreactivity of 5-[2-(pyrid-n-yl)ethenyl]oxazole (n = 2, 3 and 4)

Autori
Botti, V. ; Elisei, F. ; Faraguna, Fabio ; Marinić, Željko ; Mazzucato, U. ; Šagud, Ivana ; Šindler-Kulyk, Marija ; Spalletti, A.

Izvornik
Journal of photochemistry and photobiology. A, Chemistry (1010-6030) 329 (2016); 262-272

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Photochemistry ; Pyridine ; Quantum-mechanical calculations

Sažetak
This paper describes the results obtained in the study of the photobehaviour of heteroanalogs of stilbene bearing oxazole and pyridine rings at the opposite sides of the ethene moiety. The effect of the positional isomerism of the n-pyridyl group (n = 2, 3 and 4) on the competitive relaxation processes of the excited states (fluorescence, isomerization and cyclization) was investigated and compared with the behaviour previously reported for the 5-styryloxazole analogue. The group in Zagreb prepared the compounds and followed their photochemistry in preparative conditions while the group in Perugia studied the spectral properties of the trans/cis isomers and the cyclization products and measured the quantum yields of the competitive processes in mild conditions with the main aim to clarify the mechanism of the primary stages after excitation. The photobehaviour revealed an important deactivation effect of the n, π* states introduced by the nitrogen atom. This effect reflects the one reported for styrylpyridines, the analogous compounds with a phenyl instead of an oxazolyl ring. Quantum-mechanical Hyperchem calculations proved to be useful to describe the conformational equilibria and the role of conformers on photoreactivity while more refined DFT calculations on the Z isomers allowed the structure dependent competition between their isomerization/cyclization processes and the possible role of intramolecular H-bonds on the deactivation pathways to be explained. For the compound with n = 4, side processes of hydrogen shift in the primary dihydrophenanthrene-like intermediate and of solvent addition accompanying the photocyclization process were evidenced.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
125-0982933-2926 - Heteropolicikli, strukturne osnove za bioaktivne spojeve. Sinteza i fotokemija (Irena Škorić, )

Ustanove
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb

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


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