AL ANSHORI, Jamaludin, Tomáš SLANINA, Eduardo PALAO UTIEL and Petr KLÁN. The internal heavy-atom effect on 3-phenylselanyl and 3-phenyltellanyl BODIPY derivatives studied by transient absorption spectroscopy. PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES. CAMBRIDGE: ROYAL SOC CHEMISTRY, vol. 15, No 2, p. 250-259. ISSN 1474-905X. doi:10.1039/c5pp00366k. 2016.
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Basic information
Original name The internal heavy-atom effect on 3-phenylselanyl and 3-phenyltellanyl BODIPY derivatives studied by transient absorption spectroscopy
Authors AL ANSHORI, Jamaludin (360 Indonesia, belonging to the institution), Tomáš SLANINA (203 Czech Republic, belonging to the institution), Eduardo PALAO UTIEL (724 Spain, belonging to the institution) and Petr KLÁN (203 Czech Republic, guarantor, belonging to the institution).
Edition PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, CAMBRIDGE, ROYAL SOC CHEMISTRY, 2016, 1474-905X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10403 Physical chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.344
RIV identification code RIV/00216224:14310/16:00089981
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1039/c5pp00366k
UT WoS 000370421800012
Keywords in English SINGLET OXYGEN GENERATION; TRIPLET EXCITED-STATE; FLUORESCENT-PROBE; LIVING CELLS; PHOTODYNAMIC THERAPY; UP-CONVERSION; DYES; PHOSPHORESCENCE; DESIGN; THIOLS
Tags AKR, rivok
Tags International impact, Reviewed
Changed by Changed by: Ing. Andrea Mikešková, učo 137293. Changed: 14/4/2017 14:50.
Abstract
Three monosubstituted 3-phenylselanyl and 3-phenyltellanyl BODIPY derivatives were synthesized and their spectroscopic properties were characterized and compared to those of iodine and chlorine-atoms containing analogues as well as an unsubstituted BODIPY derivative. The fluorescence quantum yields were found to decrease, whereas the intersystem crossing quantum yields (Phi(ISC)), determined by transient spectroscopy, increased in the order of the H -> Cl -> Se/I -> Te substitution. The maximum Phi(ISC), found for the 3-phenyltellanyl derivative, was 59%. The results are interpreted in terms of the internal heavy-atom effect of the substituents.
Links
LM2011028, research and development projectName: RECETOX ? Národní infrastruktura pro výzkum toxických látek v prostředí
Investor: Ministry of Education, Youth and Sports of the CR
LO1214, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX)
Investor: Ministry of Education, Youth and Sports of the CR
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