Synthesis and structure-physicochemical properties relationship of thiophene-substituted bis(5,4-d)thiazoles

Authors

  • Zita Tokárová
  • Anna Biathová

DOI:

https://doi.org/10.2478/nbec-2018-0020

Keywords:

Chemosenzors, π-conjugation, Dithioxamide, Fluorescence, Structure-physicochemical properties, Thiazolothiazole, Thiazolo[5,4-d]thiazole, Thiophene-2-carbaldehydes, UV-Vis

Abstract

Substituted thiophene-2-carbaldehydes 1a-dwere utilized in the synthesis of symmetrically substituted thiazolo[5,4-d]thiazoles 3a-d. Bis(5,4-d)thiazoles with thiophene core at the termini are the most employed in the chemistry of materials but exhibit insufficient solubility in majority of organic solvents with notable impact on the low yields of products. Accordingly, the synthetic approach towards 2,5-dithiophen- 2-yl-thiazolo[5,4-d]thiazole (3a) and its substituted derivatives 3b-d is discussed under the various reaction conditions. Appropriate structural characterisations are included with emphasis on relationship between structure and physicochemical properties highlighting the UV-Vis and fluorescence.

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Published

2019-01-18

How to Cite

Tokárová, Z. ., & Biathová, A. . (2019). Synthesis and structure-physicochemical properties relationship of thiophene-substituted bis(5,4-d)thiazoles. Nova Biotechnologica Et Chimica, 17(2), 193–200. https://doi.org/10.2478/nbec-2018-0020

Issue

Section

Research Articles