Pregled bibliografske jedinice broj: 590110
Very Efficient New Examples of Excited State Intramolecular Proton Transfer (ESIPT) to Carbon
Very Efficient New Examples of Excited State Intramolecular Proton Transfer (ESIPT) to Carbon // XXIV IUPAC Symposium on photochemistry : abstracts
Coimbra, 2012. str. 88-88 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Very Efficient New Examples of Excited State Intramolecular Proton Transfer (ESIPT) to Carbon
Autori
Basarić, Nikola ; Došlić, Nađa ; Ivković, Jakov ; Wang, Yu-Hsuan ; Veljković, Jelena ; Mališ, Momir ; Mlinarić-Majerski, Kata ; Wan, Peter
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
XXIV IUPAC Symposium on photochemistry : abstracts
/ - Coimbra, 2012, 88-88
Skup
IUPAC Symposium on photochemistry (24 ; 2012)
Mjesto i datum
Coimbra, Portugal, 15.07.2012. - 20.07.2012
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
ESPIT; fenilnaftoli; naftilfenoli; fluorescencija
(ESPIT; phenylnaphthols; naphthylphenols; fluorescence)
Sažetak
Excited state intramolecular proton transfer (ESIPT) occurs in molecules wherein functional groups that exhibit enhanced acidity and/or basicity upon electronic excitation are in close proximity. The ESIPT has been the topic of intensive research because of its fundamental value, as well as many applications.[1] The most common acidic group in the ESIPT reactions is the phenolic OH, whereas the basic site is usually a heteroatom such as pyridine or imidazole nitrogen. Proton transfer to carbon atoms is usually considered intrinsically slow, and therefore, inefficient. Nevertheless, ESIPT from the phenol OH to the carbon atom of an adjacent phenyl, naphthyl, anthryl or pyrenyl ring have been reported.[2] However, in all reported examples involving ESIPT to carbon, the efficiency of the process is low. Herein we report on an investigation of ESIPT and solvent-assisted PT in a series of phenylnaphthols and naphthylphenols 1-6. The process was investigated by preparative irradiations in the presence of D2O wherein regiospecific incorporation of deuterium at C-atoms highlights the basic sites. In addition, photophysical properties of 1-6 were investigated by steady state and time-resolved fluorescence. The experimental observations were rationalized by ab initio calculations.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
02.05/25 - Fotokemija policikličkih molekula: od istraživanja mehanizama reakcije do novih lijekova i medicinskih primjena (Basarić, Nikola, HRZZ ) ( CroRIS)
098-0352851-2921 - Kontrola atomske i molekulske dinamike oblikovanim elektromagnetskim poljima (Došlić, Nađa, MZOS ) ( CroRIS)
098-0982933-2911 - Kavezasti spojevi: ugradbene jedinice u molekularnim sustavima (Majerski, Kata, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Kata Majerski
(autor)
Momir Mališ
(autor)
Jelena Veljković
(autor)
Nađa Došlić
(autor)
Nikola Basarić
(autor)