Pregled bibliografske jedinice broj: 391891
Photochemical dimerization of 2-vinylthiophene derivates bearing electron withdrawing groups
Photochemical dimerization of 2-vinylthiophene derivates bearing electron withdrawing groups // Journal of Photochemistry and Photobiology. A, 134 (2000), 3; 147-154 (međunarodna recenzija, članak, znanstveni)
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Naslov
Photochemical dimerization of 2-vinylthiophene derivates bearing electron withdrawing groups
Autori
D'Auria, Maurizio ; Emanuele, Lucia ; Mauriello, Giacomo ; Racioppi, Rocco
Izvornik
Journal of Photochemistry and Photobiology. A (1010-6030) 134
(2000), 3;
147-154
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
LUMO-S0; HOMO-S0; LSOMO-S1; HSOMO-T1; dimer
Sažetak
The photochemical dimerisation of 1, 3-diheteroaryl-2-propen-1-one derivatives gave a mixture of dimers in agreement with the hypothesis that the reaction is under frontier orbitals control and preferential formation of only the more stable isomers. On the contrary, the reaction of 2-heteroaryl-nitroethylene derivatives were not observed to give cyclobutane dimers but only coupling products with the loss of one nitro group. This behaviour is in agreement with the nature of the HOMO– LUMO orbitals which do not allow the superimposition of the reagents. This result allows to formulate the hypothesis that the photochemical dimerisation of 1-heteroaryl-2-EWG-ethylenes must occur as a concerted reaction. Finally, 2-heteroaryl-1, 1-dicyanoethylene derivatives gave the corresponding dimers. Also in this case, we obtained only the head-to-head dimer and the more stable one.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
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