Abstract

Two yellow bis-azo dyes containing anthracene and two azodiphenylether groups (BPA and BTA) were prepared, and an extensive investigation of their physical, thermal and biological properties was carried out. The chemical structure was confirmed by the FTIR spectra, while from the UV–Vis spectra, the quantum efficiency of the laser fluorescence at the 476.5 nm was determined to be 0.33 (BPA) and 0.50 (BTA). The possible transitions between the energy levels of the electrons of the chemical elements were established, identifying the energies and the electronic configurations of the levels of transition. Both crystals are anisotropic, the optical phenomenon of double refraction of polarized light (birefringence) taking place. Images of maximum illumination and extinction were recorded when the crystals of the bis-azo compounds rotated by 90° each, which confirms their birefringence. A morphologic study of the thin films deposited onto glass surfaces was performed, proving the good adhesion of both dyes. By thermal analysis and calorimetry, the melting temperatures were determined (~224–225 °C for both of them), as well as their decomposition pathways and thermal effects (enthalpy variations during undergoing processes); thus, good thermal stability was exhibited. The interaction of the two compounds with collagen in the suede was studied, as well as their antioxidant activity, advocating for good chemical stability and potential to be safely used as coloring agents in the food industry.

Highlights

  • Today, the colouring materials such as dyes and pigments are often synthesised and widely investigated for their useful assets and applications in various industrial sectors [1,2,3]

  • The azoic compounds [2] are a well-known class of substances, which are frequently employed in specific applications for their physical and biological properties [4,5,6,7,8,9]: as liquid crystals [10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28], industrial [29,30,31,32,33,34,35,36,37,38,39] and food colouring agents [40,41,42,43,44,45], pharmaceuticals [35,36,46,47,48,49,50,51,52,53,54,55,56,57], etc

  • We report the synthesis of two bis-azo compounds of anthracene: (i) before decomposition at 224.4 ◦ C (BPA) which stands for the 9,10-bis(((40 -phenyldiazenyl)[1,10 -biphenyl]-4-yl)oxy)methyl)anthracene and (ii) BTA which stands for the 9,10-bis(((40 -ptolyldiazenyl)-[1,10 -biphenyl]-4-yl)oxy) methyl)anthracene

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Summary

Introduction

The colouring materials such as dyes and pigments are often synthesised and widely investigated for their useful assets and applications in various industrial sectors [1,2,3]. Stability is related to the photochemical [59], thermal [45,59,64,69,70] or enzymatic [59,69] decomposition of the azo compound. Yellow dyes such as tartrazine or sunset yellow have been employed extensively in the food-colouring sector [42], while new candidates are always welcomed; if they prove to have improved physical properties and accomplish safety standards, they may be further used for food preservation, preparation and consumption. If compared to natural dyes, the synthetic ones have to be extensively investigated in order to limit their possible harmful impact on human health and the environment, translating into higher vending costs [2]

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