One- and two-photon-induced isomerization of styryl compounds possessing A-π-A' structure
Beata Jędrzejewska , Marta Gordel , Małgorzata A. Kaczorowska , Janusz Szeremeta , Marek Józefowicz , Marek Samoć
AbstractTwo styryl compounds with A-π-A′ structure that feature a fixed pyridine ring as an electron acceptor (A) and pyridine or 5,6,7,8-tetrahydroisoquinoline cation as the other acceptor (A′) have been synthesized. Their structures were elucidated by means of NMR and IR spectroscopy. One-photon fluorescence, fluorescence quantum yields and lifetimes were investigated. It was found that both visible (408 nm) and near-infrared (800 nm) light promotes the conversion of the E-isomer of the studied compounds to the Z-isomer. Under the UV irradiation (310 nm) the obtained Z-isomer reverts to the initial form in tens of minutes. The observed inter-conversion was found to be fast and efficient. The trans-to-cis isomerization was followed by decomposition of the compound upon longer than 100 s exposure to light as indicated from mass spectra.
|Journal series||Dyes and Pigments, ISSN 0143-7208, (A 40 pkt)|
|Publication size in sheets||0.5|
|Keywords in English||styryl dyes, synthesis, one- and two-photon induced, isomerization|
|Score|| = 40.0, 20-12-2017, ArticleFromJournal|
= 40.0, 20-12-2017, ArticleFromJournal
|Publication indicators||: 2016 = 3.473 (2) - 2016=3.417 (5)|
* presented citation count is obtained through Internet information analysis and it is close to the number calculated by the Publish or Perish system.