Abstract:This article describes the synthesis and characteristics of a cyanofluorene–acetylene conjugate based blue emitter C3FLA-2. In the host doped device, C3FLA-2 shows an EQE of 8.0% and CIExy of (0.156, 0.048).
“…It is interesting to compare the absorption spectrum of 4b with the that of a previously reported compound containing a cyanofluorene unit instead of a cyanocarbazole unit . The slight increment in the absorption maximum of 4b is attributed to the electron richness of carbazole relative to fluorene.…”
Section: Resultsmentioning
confidence: 89%
“…Thus, the dye containing triphenylamine, 4d , exhibited a very low oxidation potential. It is interesting to compare the electrochemical behavior of 4b with that of the previously reported dye containing a cyanofluorene core instead of a cyanocarbazole core . The comparatively low oxidation potential of 4b is attributable to the electron richness of the carbazole core relative to that of the fluorene core.…”
Section: Resultsmentioning
confidence: 97%
“…Secondly, the dipolar relaxation is less pronounced, as the donor strength of carbazole is small compared with that of triphenylamine. The redshifted emission observed for 4b compared with that of its cyanofluorene analogue indicates the elongated π conjugation rendered by the carbazole scaffold over that for fluorene.…”
New organic materials containing a cyano‐functionalized carbazole moiety at one end linked to different chromophores such as fluorene, carbazole, and triphenylamine at the other end through an acetylene spacer are synthesized and characterized by photophysical, electrochemical, thermal, and electroluminescence studies. A meta‐like linkage at the C‐2 and C‐7 atoms of the central carbazole moiety and the choice of chromophore restricted the emission to the near‐ultraviolet region. The photophysical properties of the compounds depend on the nature of the chromophore attached to the carbazole unit. A triphenylamine‐substituted derivative exhibited the longest wavelength emission in the series, attributable to the elongated conjugation and electron richness of triphenylamine, whereas the phenyl‐ and fluorene‐functionalized molecules showed the shortest wavelength emissions with vibronic patterns. The compounds containing carbazole and triphenylamine units exhibited positive solvatochromism in their fluorescence spectra, and this behavior is characteristic of charge transfer from a donor to an acceptor. A fluorene derivative containing cyano substituents at the carbazole and fluorene moieties exhibited the best electroluminescence characteristics in the series, probably because of balanced charge transport and effective confinement of the excitons in the emissive layer.
“…It is interesting to compare the absorption spectrum of 4b with the that of a previously reported compound containing a cyanofluorene unit instead of a cyanocarbazole unit . The slight increment in the absorption maximum of 4b is attributed to the electron richness of carbazole relative to fluorene.…”
Section: Resultsmentioning
confidence: 89%
“…Thus, the dye containing triphenylamine, 4d , exhibited a very low oxidation potential. It is interesting to compare the electrochemical behavior of 4b with that of the previously reported dye containing a cyanofluorene core instead of a cyanocarbazole core . The comparatively low oxidation potential of 4b is attributable to the electron richness of the carbazole core relative to that of the fluorene core.…”
Section: Resultsmentioning
confidence: 97%
“…Secondly, the dipolar relaxation is less pronounced, as the donor strength of carbazole is small compared with that of triphenylamine. The redshifted emission observed for 4b compared with that of its cyanofluorene analogue indicates the elongated π conjugation rendered by the carbazole scaffold over that for fluorene.…”
New organic materials containing a cyano‐functionalized carbazole moiety at one end linked to different chromophores such as fluorene, carbazole, and triphenylamine at the other end through an acetylene spacer are synthesized and characterized by photophysical, electrochemical, thermal, and electroluminescence studies. A meta‐like linkage at the C‐2 and C‐7 atoms of the central carbazole moiety and the choice of chromophore restricted the emission to the near‐ultraviolet region. The photophysical properties of the compounds depend on the nature of the chromophore attached to the carbazole unit. A triphenylamine‐substituted derivative exhibited the longest wavelength emission in the series, attributable to the elongated conjugation and electron richness of triphenylamine, whereas the phenyl‐ and fluorene‐functionalized molecules showed the shortest wavelength emissions with vibronic patterns. The compounds containing carbazole and triphenylamine units exhibited positive solvatochromism in their fluorescence spectra, and this behavior is characteristic of charge transfer from a donor to an acceptor. A fluorene derivative containing cyano substituents at the carbazole and fluorene moieties exhibited the best electroluminescence characteristics in the series, probably because of balanced charge transport and effective confinement of the excitons in the emissive layer.
“…Recently, various blue emitters such as anthracene [12], fluorine [13], and carbazole [14,15], were developed to improve the EL efficiencies and life time for the practical applications. Among those are fluoranthene and triphenylene derivatives.…”
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