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Elsevier, Dyes and Pigments, 3(80), p. 329-336

DOI: 10.1016/j.dyepig.2008.08.001

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Synthesis and optical properties of novel, thermally stable phenanthrolines bearing an arylthienyl-imidazo conjugation pathway

This paper is available in a repository.
This paper is available in a repository.

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Abstract

Six new hyperpolarizable chromophores based on functionalized arylthiophene donors and an imidazo-phenanthroline acceptor moiety have been designed and synthesized for the first time in good to excellent yields by condensation of 5,6-phenantroline-dione with formyl-arylthiophene derivatives in the presence of ammonium acetate in glacial acetic acid. The thermal stability, solvatochromic and nonlinear optical properties of these compounds were evaluated.