![[3,3¿]Bicarbazolyl-, triphenylamine and 1,3,5-triazine based compounds - Vaitkeviciene, Violeta](https://bilder.buecher.de/produkte/30/30850/30850937z.jpg "[3,3¿]Bicarbazolyl-, triphenylamine and 1,3,5-triazine based compounds - Vaitkeviciene, Violeta")
Andere Kunden interessierten sich auch für
![Synthesis and Characterizations of New S-Triazine Based Derivatives]( "Synthesis and Characterizations of New S-Triazine Based Derivatives")
Synthesis and Characterizations of New S-Triazine Based Derivatives26,99 €![5-nitro isatin heterocyclic derivatives and study some applications]( "5-nitro isatin heterocyclic derivatives and study some applications")
5-nitro isatin heterocyclic derivatives and study some applications59,99 €![Study of s-triazine derivatives]( "Study of s-triazine derivatives")
Study of s-triazine derivatives26,99 €![Studies on s-triazine as anti-HIV and anti-cancer agents]( "Studies on s-triazine as anti-HIV and anti-cancer agents")
Studies on s-triazine as anti-HIV and anti-cancer agents36,99 €![Antimicrobial activity of s-triazine derivatives]( "Antimicrobial activity of s-triazine derivatives")
Antimicrobial activity of s-triazine derivatives26,99 €![Heterocyclic Compounds (Pyrazolo[1,5-a]pyrimidine and 1,2,4-Triazine)]( "Heterocyclic Compounds (Pyrazolo[1,5-a]pyrimidine and 1,2,4-Triazine)")
Heterocyclic Compounds (Pyrazolo[1,5-a]pyrimidine and 1,2,4-Triazine)30,99 €![Synthesis Of Some New S-triazine Derivatives]( "Synthesis Of Some New S-triazine Derivatives")
Synthesis Of Some New S-triazine Derivatives30,99 €
![Heterocyclic Compounds (Pyrazolo[1,5-a]pyrimidine and 1,2,4-Triazine)](https://bilder.buecher.de/produkte/61/61128/61128302m.jpg "Heterocyclic Compounds (Pyrazolo[1,5-a]pyrimidine and 1,2,4-Triazine)")
Optoelectronic devices fabricated from organic low-molar-mass and polymeric materials are gaining recognition and attention of the electro-optical industrial community. The most widely used building blocks of hole-transporting polymers and molecular glasses are aromatic amino groups and carbazolyl group in particular. Carbazolyl fragment is interesting as a building block in the design and synthesis of electroactive materials for the following reasons: (1) carbazole is rather cheap starting material; (2) it is a fully aromatic unit providing a good chemical, electrochemical and environmental stability; (3) it can be easily substituted with a wide variety of functional groups to help the solubility and to tune the optical and electrical properties. [3,3 ]Bicarbazolyl unit is much less studied and used in the design and synthesis of organic semiconductors and other electroactive materials. New macromolecular and low-molar-mass charge-transporting compounds containing [3,3 ]bicarbazolyl and aromatic amino moieties with different arylamino groups as substituents have been synthesized. The thermal, optical and photoelectrical properties of the obtained materials have been studied.