Pregled bibliografske jedinice broj: 873601
PHOTOCHEMISTRY OF THIOPHENE AND PYRIDINE DERIVATIVES OF BUTADIENE
PHOTOCHEMISTRY OF THIOPHENE AND PYRIDINE DERIVATIVES OF BUTADIENE // XXV.Hrvatski sastanak kemičara i kemijskih inženjera, Poreč, 2017, Knjiga sažetaka / Ana Šantić, Marijana Đaković (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2017. str. 139-139 (poster, nije recenziran, sažetak, ostalo)
CROSBI ID: 873601 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
PHOTOCHEMISTRY OF THIOPHENE AND PYRIDINE DERIVATIVES OF BUTADIENE
Autori
Levačić, Marko ; Šagud, Ivana ; Škorić, Irena
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
XXV.Hrvatski sastanak kemičara i kemijskih inženjera, Poreč, 2017, Knjiga sažetaka
/ Ana Šantić, Marijana Đaković - Zagreb : Hrvatsko kemijsko društvo, 2017, 139-139
Skup
XXV.Hrvatski sastanak kemičara i kemijskih inženjera, Poreč, 2017,
Mjesto i datum
Poreč, Hrvatska, 19.04.2017. - 22.04.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
photochemistry, tiophene, pyridine, bicyclo
Sažetak
Through the years a detailed study of reactivity of stilbene and as continuation butadiene derivatives was conducted in our research group. The energy that is needed for cycloaddition reactions to take place in these conjugated systems can be supplied by photochemical excitation or thermal one. These previously studied butadiene derivatives showed diverse behavior in excited state and gave new polycyclic structures as products. Products with bicyclo[3.2.1]octane skeleton were present in almost all of the irradiation experiments. These structures are widely present in a vast number of biologically active compounds and are hard to obtain in ground state chemistry. Research was further extended to include new heterocyclic rings into the butadiene structure. Thiophene and pyridine rings were included, and new compounds were successfully synthesized and characterized Compounds 1 and 2 were investigated and in excited state gave polycyclic products that were completely characterized. As the yields of the transformations were good and all of the polycyclic products were isolated and characterized the next step was to determine the quantum yields for these cycloaddition reactions. To determine the quantum yields chemical actinometry was utilized. We used ferrioxalate actinometer as well as potassium iodide actinometer to gain valid reproducible results. In order to conduct these measurements GC-MS and HPLC-MS systems were used.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb