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Seven new donor/acceptor oligothiophenes 1-2 were synthesized by Stille coupling in moderate to good yields. Compounds 1-2 were completely characterized by the usual spectroscopic methods. In agreement with the electrochemical and the spectroscopic studies for this compounds the new derivatives prepared, can find application for manufacturing new materials with strong non-linear optical (NLO) properties.

Abstract. The synthesis of thienyl-substituted pyrrole azo dyes and their UV-visible, solvatochromic and electrochemical properties are described. In agreement with the solvatochromic data and also with the electrochemical study the new donor-acceptor systems synthesized could have applications in NLO.

The encapsulation of Cu(II) purine derivative complex was carried out by ion exchange of the complex from aqueous solutions into zeolite NaY. The entrapped complex was characterized by spectroscopic methods (FTIR and ICP-AES) and surface analysis (XRD). The various techniques of characterization used show that the Cu(II) complex was effectively encapsulated in the zeolite and this process does not modify the morphology and structure of the NaY zeolite. These materials have potential applications in heterogeneous catalysis in mild reaction conditions.

New tricyanovinyl-derivatives 1 of 1-(alkyl)aryl-2-(2'-thienyl)pyrroles 2 have been synthesized and characterized. Compounds 1 display dramatic reductions in both their optical and electrochemical band gaps in comparison to thienylpyrroles 2. The solvatochomic behavior of tricyanovinyl-derivatives 1 was investigated in a variety of solvents. In agreement with the solvatochromic and the electrochemical studies for pushpull derivatives I the new compounds prepared, can find application for manufacturing new materials with notable non-linear optical properties.