178115-29-2Relevant academic research and scientific papers
Switch-On Fluorescence of a Perylene-Dye-Functionalized Metal-Organic Framework through Postsynthetic Modification
Dietl, Christian,Hintz, Henrik,Rühle, Bastian,Auf Der Ginne, Schmedt J?rn,Langhals, Heinz,Wuttke, Stefan
, p. 10714 - 10720 (2015)
A perylene dye was introduced directly as a linker into a metal-organic framework (MOF) during synthesis. Depending on the dye concentration in the MOF synthesis mixture, different fluorescent materials were generated. The successful incorporation of the
Synthesis and photophysical studies of triazine-linked porphyrin-perylene bisimide dyad with long-lived perylene triplet state
Zhou, Xueqin,Liu, Dongzhi,Wang, Tianyang,Hu, Xiaoxia,Guo, Jianfeng,Weerasinghe, Krishanthi C.,Wang, Lichang,Li, Wei
, p. 57 - 63 (2014)
Porphyrin-perylene bisimide dyad containing a triazine group as the linker was synthesized and characterized. The absorption spectra reveal that there is no appreciable interaction between the ground-state porphyrin and ground-state perylene. The fluoresc
One-step synthesis of unsymmetrical N -Alkyl- N '-aryl perylene diimides
Robb, Maxwell J.,Newton, Brandon,Fors, Brett P.,Hawker, Craig J.
, p. 6360 - 6365 (2014/07/21)
An efficient and facile protocol for the synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides is reported that circumvents the need for multiple reaction steps. A number of unsymmetrical perylene diimides containing a solubilizing swallowtail alky
Turn-on fluorescence triggered by selective internal dye replacement in MOFs
Wuttke, Stefan,Dietl, Christian,Hinterholzinger, Florian M.,Hintz, Henrik,Langhals, Heinz,Bein, Thomas
supporting information, p. 3599 - 3601 (2014/04/03)
Coordinatively unsaturated metal sites (CUS) are used to create dye-functionalized metal-organic frameworks (MOFs). The quenching of dye fluorescence through interactions with the CUS can be utilised for chemical sensing of Lewis bases that displace the d
On/off switching of perylene tetracarboxylic bisimide luminescence by means of substitution at the N-position by electron-rich mono-, Di-, and trimethoxybenzenes
Flamigni, Lucia,Ventura, Barbara,Barbieri, Andrea,Langhals, Heinz,Wetzel, Fritz,Fuchs, Kerstin,Walter, Andreas
experimental part, p. 13406 - 13416 (2011/02/24)
A series of perylene tetracarboxylic bisimides, substituted at the N-position with methoxyphenyl groups, have been synthesized together with model compounds and their photophysical properties have been investigated by means of steady-state and time-resolv
The identification of carbonyl compounds by fluorescence: A novel carbonyl-derivatizing reagent
Langhals, Heinz,Jona, Wolfgang
, p. 2110 - 2116 (2007/10/03)
Fluorescent hydrazones are afforded by the reaction of the nonfluorescent N-aminoperylene-3,4:9,10-tetracarboxylic-bisimides with ketones and aldehydes; thus we obtain a fluorescent derivatization for the qualitative and semiquantitative determination of
