“…This phenomenon is similar to that for N-triazinyl derivatives of aminopyrenes [4]. The strong fluorescence quenching of dichlorotriazinyl derivatives is the most remarkable feature.…”
Section: Absorption and Fluorescence Propertiesmentioning
confidence: 54%
“…Compound 3 was synthesized by treatment of 2 with acetic anhydride according to a literature procedure for synthesis of Nacetyl-2-aminopyrene with a slight modification [4]. The product was obtained in a high yield and purity.…”
Section: Synthesismentioning
confidence: 99%
“…In previous papers [2,3] we reported on the synthesis and solvent effect on absorption and fluorescence spectra, fluorescence lifetime and fluorescence quantum yield of N-triazinyl derivatives of 3-aminobenzanthrone. Recently, we have described spectral and photophysical characteristics of N-triazinyl derivatives of 1-and 2-aminopyrenes [4]. Presently we are studying the properties of the bichromophore of the D-T-A type with 3-aminoperylene as the EET acceptor.…”
“…This phenomenon is similar to that for N-triazinyl derivatives of aminopyrenes [4]. The strong fluorescence quenching of dichlorotriazinyl derivatives is the most remarkable feature.…”
Section: Absorption and Fluorescence Propertiesmentioning
confidence: 54%
“…Compound 3 was synthesized by treatment of 2 with acetic anhydride according to a literature procedure for synthesis of Nacetyl-2-aminopyrene with a slight modification [4]. The product was obtained in a high yield and purity.…”
Section: Synthesismentioning
confidence: 99%
“…In previous papers [2,3] we reported on the synthesis and solvent effect on absorption and fluorescence spectra, fluorescence lifetime and fluorescence quantum yield of N-triazinyl derivatives of 3-aminobenzanthrone. Recently, we have described spectral and photophysical characteristics of N-triazinyl derivatives of 1-and 2-aminopyrenes [4]. Presently we are studying the properties of the bichromophore of the D-T-A type with 3-aminoperylene as the EET acceptor.…”
“…Synthesis of 1-nitropyrene, 1-aminopyrene, N-(4,6-dichloro-1,3,5-triazin-2-yl)-1-aminopyrene (1) and N-(4,6-dichloro-1,3,5-triazin-2-yl)-3-aminobenzanthrone (4) was performed according to literature procedures [3,4].…”
Section: Synthesismentioning
confidence: 99%
“…Kapusta et al [3] and Šoustek et al [4] have reported on the synthesis and photo-physics of N-substituted 3-aminobenzanthrones and N-substituted 1-aminopyrenes respectively, i.e. of relevant component model compounds.…”
Play the field: A field‐effect transistor using reduced graphene oxides was prepared through the reduction of graphene oxides connected between two electrodes. The use of pyrene with an electron‐withdrawing group and an electron‐donating group showed the p‐ and n‐doping effects, respectively, while the pyrene backbone with no electron‐withdrawing or ‐donating groups showed no doping effect.
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