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Tuning photophysical and electroluminescent properties of phenanthroimidazole decorated carbazoles with donor and acceptor units: Beneficial role of cyano substitution
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Tuning photophysical and electroluminescent properties of phenanthroimidazole decorated carbazoles with donor and acceptor units: Beneficial role of cyano substitution

Anuj Sharma, Rajendiran Balasaravanan, K.R. Justin Thomas, Mangey Ram, Deepak Kumar Dubey, Rohit Ashok Kumar YadavJwo-Huei Jou
Dyes and Pigments, 卷.184, 108830
01/2021

摘要

Acidochromism Aggregation-induced emission (AIE) Carbazole Charge transfer transition Organic-light emitting diodes (OLEDs) phenanthro[9,10-d]imidazole Chemical Engineering (all) Process Chemistry and Technology
Four new multi-functionalized carbazole derivatives featuring phenanthroimidazole, N-phenylcarbazole and cyano-substituents are designed and synthesized. The dyes are characterized by photophysical, electrochemical and thermal properties and the dependency of auxiliary chromophores on the functional properties critically analyzed. The dyes showed tunable emission from violet to blue region depending on the chromophore attached to the carbazole core. The cyano-substituted dyes exhibited enhanced intramolecular charge transfer in optical properties as compared to N-phenylcarbazole substituted dyes. Consequently, cyano-substituted dyes displayed solvatochromism in emission and possess large Stokes shift. All the dyes showed remarkable thermal stability attributable to robust phenanthroimidazole and carbazole chromophores. The fluorescent sensory properties of all the dyes toward acid are also explored and found that the emission of cyano derivatives displayed blue shift due to protonation of phenanthroimidazole unit. Finally, the dyes are employed as dopant emitter in multilayer solution-processed organic light-emitting diode which displayed blue electroluminescence.

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