2013
DOI: 10.1007/s11051-013-1739-6
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Porphyrin synthesized from cashew nut shell liquid as part of a novel superparamagnetic fluorescence nanosystem

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Cited by 20 publications
(9 citation statements)
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“…Based on these considerations, and those in previous works from our group regarding the preparation of meso -porphyrins [18,21,23,24,25,26], we report the synthesis of cardanol-derivate porphyrins with respect to its application as an emitting layer in OLEDs. The photophysical and electrochemical properties of the porphyrins are investigated in solution and in thin film, and we also investigate the use of these compounds as emitters in simple OLED devices through electroluminescence analysis.…”
Section: Introductionmentioning
confidence: 89%
“…Based on these considerations, and those in previous works from our group regarding the preparation of meso -porphyrins [18,21,23,24,25,26], we report the synthesis of cardanol-derivate porphyrins with respect to its application as an emitting layer in OLEDs. The photophysical and electrochemical properties of the porphyrins are investigated in solution and in thin film, and we also investigate the use of these compounds as emitters in simple OLED devices through electroluminescence analysis.…”
Section: Introductionmentioning
confidence: 89%
“…Generally, the weaker the emission spectrum of semiconductor materials, the higher the rate of separation of photoinduced charge carriers and, possibly, the higher the photocatalytic activity [ 44 ]. Moreover, it is worth noting that the emission spectrum of the sample H 2 Pp–ZnO presented two intense peaks, respectively at 657 nm and 723 nm, attributed to the emission of pure porphyrin H 2 Pp [ 35 ]. The photoluminescent spectra of H 2 Pp and H 2 Pp–ZnO with visible light excitation can be seen in Figure S2 of the Electronic Supplementary Information (ESI) , showing that even in the presence of ZnO, H 2 Pp fluorescence was not suppressed.…”
Section: Resultsmentioning
confidence: 99%
“…The compound 5,10,15,20- tetra -[4-(2-(3-pentadecyl)phenoxy)ethoxy]phenylporphyrin ( 3 ) was synthesized according to the procedure reported in the literature [ 35 ]. It was obtained by reacting the compound 2 (2.21 mmol) with pyrrole (2.21 mmol) and NaCl (55.25 mmol).…”
Section: Methodsmentioning
confidence: 99%
“…However, there are still some challenges such as an inevitable false signal caused by non-specific adsorption in real samples. Thus, the magnetization of particles was utilized to capture and separated target agents from complex matrices to avoid false signals [106][107][108]. Furthermore, MNPs can be adopted to utilize as contrast agents for magnetic resonance imaging (MRI) [100,109,110].…”
Section: Fluorescence Spectroscopymentioning
confidence: 99%