15 research outputs found

    Functionalisation and photophysical properties of highly fluorescent Boradiazaindacene (BODIPY) derivatives

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    The objective of the work described in this thesis was the synthesis and the functionalisation at the 3,5-positions of highly fluorescent BODIPY (Borondipyrromethene) dyes. For this purpose, research has mainly focused on the synthesis of the 3,5-dichloro-BODIPY as a precursor to develop the extended 3,5-disubstitutedBODIPY derivatives using nucleophilic aromatic substitution, transition metal cross coupling reactions and to study their photophysical properties. In the first chapter, we have developed an effective and efficient synthesis of the novel 3,5-dichloro-BODIPY with different subunits at thestatus: publishe

    Synthesis of dioxolanes and oxazolidines by silica gel catalysis

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    Ethyl 2-(2,3-dioxoindolin-1-yl)acetate

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    Electrochemical behavior and in-vitro antimicrobial screening of some thienylazoaryls dyes

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    Abstract Background A series of recently reported phenolic azo dyes 7a–e were prepared by coupling the thienyl diazonium sulfate of 3-Amino-4H-benzo[f]thieno[3,4-c](2H)chromen-4-one with selected diversely substituted phenolic and naphtholic derivatives. These compounds were evaluated for their antibacterial and antifungal activities. Furthermore their voltammetric behavior was compared at a glassy carbon electrode. Results The voltammetric behavior of the five recently reported azo dyes has been compared at a glassy carbon electrode. It is shown that the azo dyes 7a–e with a hydroxyl group in the ortho position with respect to the azo bridge give rise to well defined, irreversible peaks for the oxidation and reduction process within a pH range of 2–7. The mechanisms of electrochemical oxidation of compound 7a–c and 7e are proposed. For the hydroxyl-substituted dyes, re-oxidation peaks were obtained in the subsequent scan. The antimicrobial activities of the reported compounds 7a–e along with the entire precursors 1–4 and 6a–e were performed against selected bacterial and fungal species and their activities compared to those of nystatin, griseofulvin and ciprofloxacin used as reference drugs. Conclusions The present study showed significant antimicrobial activity of compounds 6d, 7a and 7c,e against the tested microorganisms; this result confirms the antimicrobial potency of azo compounds and some of their precursors
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