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Abstract

Five new derivatives of 4,6-di(thiophen-2-yl)pyrimidine (DTP) were designed by structural modification with the aim to tune the electro-optical and charge transfer properties. The effect of oligocene and oligocenothiophene incorporation/substitution was investigated on various properties of interests. The smaller hole reorganization energy revealed that compounds 1-5 might be good hole transfer contenders. The smaller hole reorganization energy of newly designed five DTP derivatives than the pentacene showed that prior compounds might be good/comparable hole transfer materials than/to that of pentacene. The computed electron reorganization energy of DTP derivatives 1-5 are 124, 185, 93, 95 and 189 meV smaller than the meridional-tris (8-hydroxyquinoline) aluminum (mer-Alq3) illuminating that electron mobility of these derivatives might be better/comparable than/to referenced compound.
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Abstract

In recent years organic semiconductors have been given attention in the field of active materials for gas sensor applications. In the paper the investigations of the optoelectronic sensor structure of ammonia were presented. The sensor head consists of polyaniline and Nafion layers deposited on the face of the telecommunication optical fiber. The elaborated sensor structure in the form of Fabry-Perot interferometer is of the extremely small dimension – its thickness is of the order of 1 um. Many sensor structures of diffierent combinations of the polyaniline and Nafion layers were constructed and investigated. The optimal solution seems to be the structures with small number of polianiline layers (up to three).
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