TY  - JOUR
A1  - Schwarze, Thomas
A1  - Mickler, Wulfhard
A1  - Dosche, Carsten
A1  - Flehr, Roman
A1  - Klamroth, Tillmann
A1  - Löhmannsröben, Hans-Gerd
A1  - Saalfrank, Peter
A1  - Holdt, Hans-Jürgen
T1  - Systematic investigation of photoinduced electron transfer controlled by internal charge transfer and its consequences for selective PdCl2 coordination
N2  - Fluoroionophores of fluorophore-spacer-receptor format were prepared for detection of PdCl2 by fluorescence enhancement. The fluorescent probes 1-13 consist of a fluorophore group, an alkyl spacer and a dithiomaleonitrile PdCl2 receptor. First, varying the length of the alkylene spacer (compounds 1-3) revealed a dominant through-space pathway for oxidative photoinduced electron transfer (PET) in CH2-bridged dithiomaleonitrile fluoroionophores. Second, fluorescent probes 4-9 containing two anthracene or pyrene fragments connected through CH2 bridges to the dithiomaleonitrile unit were synthesized. Modulation of the oxidation potential (EOx) through electron-withdrawing or -donating groups on the anthracene moiety regulates the thermodynamic driving force for oxidative PET (GPET) in bis(anthrylmethylthio)maleonitriles and therefore the fluorescence quantum yields (f), too. The new concept was confirmed and transferred to pyrenyl ligands, and fluorescence enhancements (FE) greater than 3.2 in the presence of PdCl2 were achieved by 7 and 8 (FE=5.4 and 5.2). Finally, for comparison, monofluorophore ligands 10-13 were synthesized.
Y1  - 2010
UR  - https://publishup.uni-potsdam.de/frontdoor/index/index/docId/30596
UR  - http://www3.interscience.wiley.com/journal/26293/home
SN  - 0947-6539
ER  -