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Pregled bibliografske jedinice broj: 877363

Photochemical formation of anthracene quinone methide derivatives


Škalamera, Đani; Mlinarić-Majerski, Kata; Martin-Kleiner, Irena; Kralj, Marijeta; Oake, Jessy; Wan, Peter; Bohne, Cornelia; Basarić, Nikola
Photochemical formation of anthracene quinone methide derivatives // Journal of organic chemistry, 82 (2017), 12; 6006-6021 doi:10.1021/acs.joc.6b02735 (međunarodna recenzija, članak, znanstveni)


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Naslov
Photochemical formation of anthracene quinone methide derivatives

Autori
Škalamera, Đani ; Mlinarić-Majerski, Kata ; Martin-Kleiner, Irena ; Kralj, Marijeta ; Oake, Jessy ; Wan, Peter ; Bohne, Cornelia ; Basarić, Nikola

Izvornik
Journal of organic chemistry (0022-3263) 82 (2017), 12; 6006-6021

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

Ključne riječi
photodehydration, photodeamination, quinone methides, anthracene, laser flash photolysis, antiproliferative activity

Sažetak
Anthrols 2-7 were synthesized and their photochemical reactivity investigated by irradiations in aq. CH3OH. Upon excitation with visible light (λ > 400 nm) in methanolic solutions they undergo photodehydration or photodeamination and deliver methyl ethers, most probably via quinone methides (QMs), with methanolysis quantum efficiencies ΦR = 0.02-0.3. Photophysical properties of 2-7 were determined by steady-state fluorescence and time-correlated single photon counting. Generally, anthrols 2-7 are highly fluorescent in aprotic solvents (ΦF = 0.5-0.9), whereas in aqueous solutions the fluorescence is quenched due to excited state proton transfer (ESPT) to solvent. The exception is amine 4 that undergoes excited state intramolecular proton transfer (ESIPT) in neat CH3CN where photodeamination is probably coupled to ESIPT. Photodehydration may take place via ESIPT (or ESPT) that is coupled to dehydration, or via a hitherto undisclosed pathway that involves photoionization and deprotonation of radical-cation, followed by homolytic cleavage of the alcohol OH group from the phenoxyl radical. QMs were detected by laser flash photolysis (LFP) and their reactivity with nucleophiles investigated. Biological investigation of 2-5 on human cancer cell lines showed enhancement of antiproliferative effect upon exposure of cells to irradiation by visible light, probably due to formation of electrophilic species such as QMs.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-11-2013-5660
HRZZ-IP-2014-09-6312 - Supramolekulska kontrola fotokemijskih reakcija eliminacije (Nikola Basarić, )

Ustanove
Institut "Ruđer Bošković", Zagreb

Citiraj ovu publikaciju

Škalamera, Đani; Mlinarić-Majerski, Kata; Martin-Kleiner, Irena; Kralj, Marijeta; Oake, Jessy; Wan, Peter; Bohne, Cornelia; Basarić, Nikola
Photochemical formation of anthracene quinone methide derivatives // Journal of organic chemistry, 82 (2017), 12; 6006-6021 doi:10.1021/acs.joc.6b02735 (međunarodna recenzija, članak, znanstveni)
Škalamera, Đ., Mlinarić-Majerski, K., Martin-Kleiner, I., Kralj, M., Oake, J., Wan, P., Bohne, C. & Basarić, N. (2017) Photochemical formation of anthracene quinone methide derivatives. Journal of organic chemistry, 82 (12), 6006-6021 doi:10.1021/acs.joc.6b02735.
@article{article, year = {2017}, pages = {6006-6021}, DOI = {10.1021/acs.joc.6b02735}, keywords = {photodehydration, photodeamination, quinone methides, anthracene, laser flash photolysis, antiproliferative activity}, journal = {Journal of organic chemistry}, doi = {10.1021/acs.joc.6b02735}, volume = {82}, number = {12}, issn = {0022-3263}, title = {Photochemical formation of anthracene quinone methide derivatives}, keyword = {photodehydration, photodeamination, quinone methides, anthracene, laser flash photolysis, antiproliferative activity} }

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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