Skip to content

Advertisement

Open Access

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

  • Joseph Tsemeugne1, 2,
  • Emmanuel Sopbué Fondjo1Email authorView ORCID ID profile,
  • Jean-de-Dieu Tamokou3,
  • Ignas Tonle1,
  • Irene Chinda Kengne3,
  • Arnaud Djintchui Ngongang1,
  • Stephen Tamekou Lacmata3,
  • Taoufik Rohand4,
  • Jules Roger Kuiate3 and
  • Beibam Luc Sondengam2
Chemistry Central Journal201711:119

https://doi.org/10.1186/s13065-017-0345-6

Received: 6 September 2017

Accepted: 10 November 2017

Published: 21 November 2017

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 7ac 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.

Keywords

Azo compoundsCarbon paste electrodeCyclic voltammetryAntibacterial agentsAntifungal agents

Introduction

Before the discovery of the first synthetic organic dye in 1856, namely the Mauvaine [1], human being has to use some part of plants like roots and leaves to color textile fibers. This discovery will kick off a new area in the field of dye research and nowadays approximately all molecules used as dyes in the textile industry are synthetic with a strong fondness for diazo dyes [24]. In addition to this traditional application of dyes, other fields of interest make azo compounds a real source of hope, notably in pharmaceutical [57] and food industries [8, 9], and in dosimetry [10, 11]. In general, azo dyes are highly preferred because they attach to the fibers by forming strong covalent bonds with the hydroxyl groups of the cellulose [12], so that the process of discoloration is very difficult under the conditions where textiles are washed [13, 14]. It is also demonstrated that the degradation of the textile is linked to the action of the microorganisms that are attached to it and it is to remedy this problem that the textile industry makes increasing use of biocidal dyes such as diazo dyes [15]. The textile industry is also increasingly faced with the problem of treating wastewater polluted by the rest of the dyes that have not been fixed to the fibers during the coloring process [16]. Due to their structural complexity, azo dyes often have very low biodegradability and their biological treatments are usually expensive and generally inefficient [17]. For this purpose, electrochemical techniques are the most recommended alternative because of their high efficiency, their eco-friendliness and their relatively low cost [17]. We recently reported the synthesis of a cyclic holigomeric azo dye containing three –N=N– units alternating with three fused thienocoumarins moieties in its structure and found to possess antioxidant properties. This means that it is capable to reduce an oxidant such as Fe3+ into Fe2+ through its diazo functionalities [18], justifying thereby the use of diazo compounds in chemotherapy treatments [19, 20]. In addition, encouraged by previous promising results obtained from the biological activities studies of some of the azo compounds that we have recently reported [21], we therefore undertook to intensify our research for new azo compounds with good dyeing [5, 22], biological properties [6, 23], and which could also find interesting applications in solving some issues related to industrial environmental pollution [16]. In this work, we investigated the antimicrobial activities of five recently reported [24] azo compounds respectively on six bacterial and six fungal strains. On the other hand, in order to assess their possible applications in the textile industry waste water remediation, and the evidence concerning the mechanisms of biological electron-transfer processes we carried out the electrochemical characterization of these compounds, on the carbon electrode.

Experimental

General information

All melting points were corrected and were determined using an Electrothermal Melting Point Apparatus Model 9100, a Büchi 530 melting point apparatus and a Stuart Scientific Melting Point Apparatus SMP3. The Thin Layer Chromatography (TLCs) was carried out on Eastman Chromatogram Silica Gel Sheets (13,181; 6060) with fluorescent indicators. A mixture of ethyl acetate and methylene chloride (7:3) was used as the eluent and iodine was used for the visualization of the chromatograms. The IR spectra were measured with a Fourier Transform Infrared spectrometer JASCO FT/IR-4100 and a Perkin Elmer FT-IR 2000 spectrometer. The UV spectra were recorded with a Beckman U-640 Spectrophotometer, using samples’ solutions of concentration 2 × 10−5 mol L−1. Combustion analyses were carried out with a Euro EA CHNSO analyser from Hekatech company, and the results were found to be in good agreement (± 0.3%) with the calculated values. HREIMS were measured on mass spectrometer LCQ Classic with ESI Source from Thermo Fisher Scientific Company. 1H-NMR spectra were recorded in DMSO-d 6 with a 250 MHz spectrometer Bruker AV III. 13C-NMR spectra were recorded in DMSO-d 6 with a 62.5 MHz spectrometer Bruker AV III. Tetramethyl silane (TMS) was used as the internal reference.

Preparation of the reagents and starting materials

All the reagents mentioned in this work were purchased from Aldrich and Fluka and were used without further purification. Starting material 4 was prepared according to the procedures mentioned in the literature published earlier [25].

Preparation of diazonium salt solution

In a similar manner as described in [24] dry sodium nitrite (2.07 g, 3 mmol) was slowly added over a period of 30 min to concentrated sulphuric acid (10 mL) with occasional stirring. The solution was cooled to 0–5 °C. Compound 4 was dissolved in DMSO (10 mL) and cooled to 0–5 °C. The nitrosyl sulphuric acid solution kept at 0–5 °C was added to the solution of 4 and the temperature was maintained between 0 and 5 °C. The clear diazonium salt solution thus obtained consisting of the in situ-formed intermediate 5, was used immediately in the coupling reactions.

General procedure for the preparation of the coupling products 7a–e

Phenol derivatives 6a–e (3 mmol) were dissolved in DMSO (10 mL) and then cooled in an ice-bath at 0–5 °C. The diazonium solution of 4 previously prepared was added drop wise over 1 h, and then 15 mL of sodium acetate solution (10%) was added to the mixture. The pH of the mixtures was in the range 9–11. The solid precipitate was collected on a filter and crystallised from methanol to give the title compounds 7. The freshly prepared compounds were characterized by their physical, elemental and spectroscopic data which were found to be in full agreement with those published earlier [24].

3-[2-(2-hydroxy-1-naphthyl)diazenyl]-4H-benzo[f]thieno[3,4-c]chromen-4-one dihydrate, 7a

Reaction of diazonium salt of 4 with 6a gave compound 7a as a red powder; yield 59%, 0.41 g, mp 185.7 °C; IR (KBr) νmax: 3558, 3544 (OH), 3164, 3153 (Ar. C–H), 1718 (C=O), 1617, 1439, 1412 (N = N) cm−1. UV (THF) λmax/nm (log ε): 242 (4.54), 254 (4.61), 277 (2.46), 290 (4.19), 298 (4.11), 335 (4.49), 356 (4.54), 374 (4.64), 391 (4.56). 1H NMR (250 MHz, DMSO-d 6 ): δH 7.21 (1H, s, 1-H), 7.61 (1H, d, J 8.9 Hz, 6-H), 8.37 (1H, d, J 8.8 Hz, 7-H), 8.13 (1H, d, J 8.0 Hz, 8-H), 7.71 (1H, dd, J 7.5 and 7.5 Hz, 9-H), 7.76 (1H, dd, J 7.5 and 7.8 Hz, 10-H), 8.63 (1H, d, J 9.0 Hz, 11-H), 7.75 (1H, d, J 8.0 Hz, 3′-H), 7.98 (2H, d, J 8.0 Hz, 4′-H and 5′-H), 7.50 (1H, dd, J 7.5 and 7.0 Hz, 6′-H), 8.00 (1H, dd, J 8.8 and 8.1 Hz, 7′-H), 7.33 (1H, d, J 8.8 Hz, 8′-H), 2.51 (1H, D2O-exchangeable, OH). 13C NMR (62.50 MHz, DMSO-d 6 ): δ C 118.2 (C-1), 134.3 (C-3), 116.3 (C-3a), 166.4 (C-4), 156.8 (C-5a), 125.6 (C-6 and C-3′), 139.5 (C-7), 131.4 (C-7a), 130.2 (C-8 and C-11b), 117.3 (C-9), 129.9 (C-10), 126.8 (C-11), 137.8 (C-1′ and 11a), 103.3 (C-11c), 158.5 (C-2′), 127.8 (C-4′), 129.6 (C-4a′), 128.7 (C-5′), 118.9 (C-6′), 132.7 (C-7′), 120.8 (C-8′), 147.7 (C-8a′). MS, m/z (%) = 236 (47), 288 (30), 296 (100), 373 (40), 393 (50), 328 (100), 340 (22), 421 (22). Anal. Calcd for C25H18N2O5S (458.49): C, 65.50; H, 3.93; N, 6.11; S, 6.98. Found: C, 65.48; H, 3.91; N, 6.09; S, 6.96.

3-[2-(4-acetyl-3-hydroxy-2-naphthyl)diazenyl]-1-[2-(4-oxo-4H-benzo[f]thieno[3,4-c]chromen-3-yl)diazenyl]-4H-benzo[f]thieno[3,4-c]chromen-4-one disulphate dihydrate, 7b

Reaction of diazonium salt of 4 with 6b gave compound 7b as an orange powder; yield 28%, 0.38 g, mp 194.9 °C; IR (KBr) νmax: 3280(OH), 3076 (Ar. C–H), 1720 (C=O), 1619, 1529, 1438 (N=N) cm−1. UV (THF) λmax/nm (log ε): 240 (4.34), 253 (4.43), 293 (3.95), 328 (4.25), 343 (4.20), 360 (4.31), 373 (4.39), 388 (4.28). 1H NMR (250 MHz, DMSO-d 6 ): δH 3.45 (3H, s, CH3), 6.94 (1H, s, H-1′′), 7.41 (OH, broad s, D2O-exchangeable), 7.12 (1H, s, H-1′), 8.52 (1H, dd, J 10.53 and 10.50 Hz, H-9), 8.35 (1H, dd, J 7.75 and 6.50 Hz, H-9′′), 8.00 (1H, dd, J 9.54 and 7.50 Hz, H-10), 7.88 (1H, dd, J 8.75 and 7.45 Hz, H-6′), 7.75 (1H, dd, J 10.50 and 10.45 Hz, H-7′), 7.62 (1H, dd, J 8.00 and 7.70 Hz, H-10′′), 9.01 (1H, d, J 7.50 Hz, H-11), 8.91 (1H, d, J 8.70 Hz, H-5′), 8.75 (1H, d, J 8.00 Hz, H-11′′), 8.18 (1H, d, J 8.00 Hz, H-6′′), 7.67 (1H, d, J 11.50 Hz, H-8′), 7.55 (1H, d, J 8.00 Hz, H-7′′), 7.51 (1H, d, J 10.00 Hz, H-8), 7.50 (1H, d, J 9.00 Hz, H-7), 7.44 (1H, d, J 8.00 Hz, H-8′′), 7.33 (1H, d, J 9.00 Hz, H-6). 13C NMR (62.50 MHz, DMSO-d 6 ): δ C 164.2 (CO), 134.7 (C-1), 145.0 (C-3), 115.4 (C-3a), 157.0 (C-4), 148.5 (5a), 120.0 (C-6), 130.7 (C-7), 133.7 (C-7a), 131.6 (C-8), 122.2 (C-9), 127.8 (C-10), 124.8 (C-11), 131.0 (C-11a), 103.8 (C-11b), 114.3 (C-11c), 121.0 (C-1′), 137.0 (C-2′), 155.0 (C-3′), 113.7 (C-4′), 122.7 (C-4a′), 133.0 (C-5′), 127.8 (C-6′), 126.2 (C-7′), 128.5 (C-8′), 103.2 (C-8a′), 119.0 (C-1′′), 139.1 (C-3′′), 115.0 (C-3a′′), 156.6 (C-4′′), 148.1 (5a′′), 123.6 (C-6′′), 129.6 (C-7′′), 133.2 (C-7a′′), 119.8 (C-8′′), 121.0 (C-9′′), 128.8 (C-10′′), 126.0 (C-11′′), 130.8 (C-11a′′), 103.5 (C-11b′′), 114.0 (C-11c′′), 33.0 (CH3). MS, m/z (%) = 237 (42), 250 (62), 258 (100), 276 (45), 313 (17), 373 (80), 404 (25), 521 (22), 644 (40), 660 (10). Anal. Calcd for C42H30N4O16S4 (974.96): C, 51.74; H, 3.10; N, 5.75; S, 13.16. Found: C, 51.65; H, 3.08; N, 5.80; S, 13.18.

3-(2-{3-acetyl-2-hydroxy-5,6-bis[2-(4-oxo-4H-benzo[f]thieno[3,4-c]chromen-3 yl)diazenyl]phenyl}diazenyl)-4H-benzo[f]thieno[3,4-c]chromen-4-one trisulphate, 7c

Reaction of diazonium salt of 4 with 6c gave compound 7c as an orange powder; yield 26%, 0.65 g, mp 200.2 °C; IR (KBr) νmax: 3547 (OH), 1730 (C=O), 1517, 1435 (N=N) cm−1. UV (THF) λmax/nm (log ε): 236 (5.33), 267 (5.01), 286 (4.98), 335 (5.18), 438 (4.28), 540 (3.33). 1H NMR (250 MHz, DMSO-d 6 ): δH 9.12 (1H, br s, H-4′), 9.00 (1H, d, J 8.75 Hz, H-7″), 8.83 (1H, d, J 9.50 Hz, H-7′″), 8.60 (1H, dd, J 8.75 Hz and J’ 6.75 Hz, H-9″), 8.54 (1H, dd, J 9.50 Hz and J 6.75 Hz, H-10′″), 8.52 (1H, d, J 11.75 Hz, 8′″), 8.50 (1H, s, H-1″), 8.35 (1H, d, J 8.75 Hz, H-6″), 8.12 (1H, d, J 8.75 Hz, H-8″), 7.95 (1H, d, J 8.25 Hz, H-11″), 7.93 (1H, d, J 12.75 Hz, H-7), 7.88 (1H, dd, J 8.00 Hz and J’ 7.75 Hz, H-9), 7.82 (1H, dd, J 8.50 Hz and J’ 8.25 Hz, H-10″), 7.81 (1H, s, H-1), 7.78 (1H, d, J 12.75 Hz, H-6), 7.73 (1H, dd, J 7.50 Hz and J’ 6.50 Hz, H-9′″), 7.74 (1H, d, J 12.00 Hz, H-11′″), 7.66 (1H, dd, J 13.00 Hz and J′ 7.25 Hz, H-10), 7.60 (1H, s, H-1′″), 7.58 (1H, d, J 9.00 Hz, H-6′″), 7.91 (1H, d, J 12.75 Hz, H-11), 7.95 (1H, d, J 8.25 Hz, H-8), 2.42 (3H, s, CH 3 -CO). 13C NMR (62.50 MHz, DMSO-d 6 ): δ C 125.8 (C-1), 132.6 (C-3), 114.4 (C-3a), 164.4 (C-4), 156.5 (C-5a), 121.8 (C-6), 137.8 (C-7), 131.5 (C-7a), 128.0 (C-8), 118.0 (C-9), 120.8 (C-10), 131.1 (C-11), 115.4 (C-11a), 148.2 (C-11b), 102.0 (C-11c), 133.0 (C-1′), 157.0 (C-2′), 122.6 (C-3′), 131.0 (C-4′), 138.2 (C-5′), 157.3 (C-6′), 126.3 (C-1″), 155.0 (C-3″), 113.5 (C-3a″), 165.0 (C-4″), 156.5 (C-5a″), 119.5 (C-6″), 130.3 (C-7″), 131.0 (C-7a″), 127.5 (C-8″), 117.8 (C-9″), 123.6 (C-10″), 129.5 (C-11″), 114.4 (C-11a″), 147.6 (C-11b″), 100.4 (C-11c″), 126.8 (C-1′″), 156.1 (C-3′″), 113.8 (C-3a′″), 163.7 (C-4′″), 155.3 (C-5a′″), 120.0 (C-6′″), 136.8 (C-7′″), 131.5 (C-7a′″), 131.5 (C-8′″), 132.1 (C-9′″), 138.7 (C-10′″), 136.2 (C-11′″), 103.7 (C-11a′″), 115.0 (C-11b′″), 100.5 (C-11c′″), 165.0 (COCH3), 25.8 (COCH 3 ). MS, m/z (%) = 234 (23), 242 (63), 341 (74), 361 (54), 405 (17), 460 (100), 480 (24), 525 (10), 582 (9), 602 (4). Anal. Calcd for C53H32N6O20S6 (1265.24): C, 50.31; H, 2.55; N, 6.64; S, 15.21. Found: C, 50.29; H, 2.54; N, 6.62; S, 15.23.

3-(2-{3-(tert-butyl)-2-hydroxy-5-methoxy-4,6-bis[2-(4-oxo-4H-benzo[f]thieno[3,4-c]chromen-3-yl)diazenyl]phenyl}diazenyl)-4H-benzo[f]thieno[3,4-c]chromen-4-one sulphate monohydrate, 7d

Reaction of diazonium salt of 4 with 6d gave compound 7d as a red powder; yield 19%, 0.43 g, mp 214.8 °C; IR (KBr) νmax: 3310 (OH), 3056 (Ar. C–H), 2960 (Csp3-H), 1734 (C=O), 1617, 1480, 1458 (N=N) cm−1. UV (THF) λmax/nm (log ε): 249 (5.34), 252 (5.34), 290 (4.94), 335 (4.52), 356 (4.44), 372 (4.46). 1H NMR (250 MHz, DMSO-d 6 ): δH 7.65 (1H, s, 1-H″), 7.81 (1H, m, 6-H″), 8.64 (1H, m, 7-H″), 8.97 (1H, d, J 8.0 Hz, 8-H″), 7.87 (1H, d, J 7.5 Hz, 9-H″), 8.46 (1H, dd, J 7.5 and 8.3 Hz, 10-H″), 7.77 (1H, m, 11-H″), 7.84 (1H, s, 1-H), 7.93 (1H, d, J 8.0 Hz, 6-H), 8.58 (1H, d, J 9.3 Hz, 7-H), 8.76 (1H, dd, J 7.0 and 8.6 Hz, 8-H), 7.80 (1H, dd, J 7.5 and 7.5 Hz, 9-H), 8.34 (1H, m, 10-H), 7.90 (1H, d, J 8.0 Hz, 11-H), 7.90 (1H, s, 1′′′-H), 7.73 (1H, d, J 8.0 Hz, 6′′′-H), 8.32 (1H, m, 7′′′-H), 8.10 (1H, m, 8′′′-H), 8.00 (1H, d, J 6.8 Hz, 9′″-H), 8.44 (1H, m, 10′″-H), 8.38 (1H, m, 11′″-H), 3.60 (3H, s, OCH3), 3.21 (9H, s, CH3). 13C NMR (62.50 MHz, DMSO-d 6 ): δ C 126.6 (C-1), 147.5 (C-3), 113.0 (C-3a), 163.2 (C-4), 156.7 (C-5a), 121.0 (C-6), 137.6 (C-7), 130.7 (C-7a), 128.8 (C-8), 118.3 (C-9), 122.6 (C-10), 130.2 (C-11), 154.8 (C-11a), 115.3 (C-11b), 102.1 (C-11c), 114.6 (C-1′), 149.0 (C-2′), 121.5 (C-3′), 119.1 (C-4′), 138.3 (C-5′), 102.0 (C-6′), 126.8 (C-1″), 147.5 (C-3″), 113.2 (C-3a″), 164.3 (C-4″), 156.1 (C-5a″), 119.4 (C-6″), 135.9 (C-7″), 131.2 (C-7a″), 127.2 (C-8″), 117.6 (C-9″), 123.6 (C-10″), 129.4 (C-11″), 155.0 (C-11a″), 114.6 (C-11b″), 101.0 (C-11c″), 126.1 (C-1′″), 148.0 (C-3′″), 114.4 (C-3a′″), 163.2 (C-4′″), 155.8 (C-5a′″), 121.0 (C-6′″), 137.2 (C-7′″), 131.5 (C-7a′″), 128.0 (C-8′″), 117.6 (C-9′″), 122.0 (C-10′″), 130.0 (C-11′″), 138.3 (C-11a′″), 115.2 (C-11b′″), 103.7 (C-11c′″), 56.0 (OCH3), 18.6 (3CH3), 25.7 (C(CH3)3). MS, m/z (%) = 1131 (7), 1113 (21), 1015 (4), 985 (5), 852 (17), 799 (100), 754 (54), 736 (30), 275 (39), 261 (100). Anal. Calcd for C56H38N6O13S4 (1131.19): C, 59.46; H, 3.39; N, 7.43; S, 11.34. Found: C, 59.45; H, 3.41; N, 7.45; S, 11.35.

3-{2-[3-(tert-butyl)-4-hydroxy-5-methylphenyl]diazenyl}-4H-benzo[f]thieno[3,4-c]chromen-4-one dihydrate, 7e

Reaction of diazonium salt of 4 with 6e gave compound 7e as a red powder; yield 69%, 0.33 g, mp 217.6 °C; IR (KBr) νmax: 3177 (Ar. C–H), 2954 (Csp3-H), 1718 (C=O), 1633, 1479, 1454 (N=N) cm−1. UV (THF) λmax/nm (log ε): 241 (4.50), 259 (4.51), 290 (4.18), 398 (5.05), 403 (5.05), 409 (5.06), 441.5 (5.06), 423 (5.03). 1H NMR (250 MHz, DMSO-d 6 ): δH 7.23 (1H, s, 1-H), 7.48 (1H, d, J 7.8 Hz, 6-H), 8.34 (1H, d, J 7.8 Hz, 7-H), 8.50 (1H, d, J 7.7 Hz, 8-H), 8.33 (1H, dd, J 7.5 and 7.0 Hz, 9-H), 7.30 (1H, dd, J 6.7 and 7.4 Hz, 10-H), 8.68 (1H, d, J 7.5 Hz, 11-H), 7.65 (1H, s, 2′-H), 7.30 (1H, s, 6′-H), 3.56 (3H, s, CH3), 3.01 (9H, s, CH3). 13C NMR (62.50 MHz, DMSO-d 6 ): δ C 119.2 (C-1), 132.4 (C-3), 115.6 (C-3a), 164.5 (C-4), 155.2 (C-5a), 126.3 (C-6), 139.7 (C-7), 133.1 (C-7a), 130.1 (C-8), 120.7 (C-9), 128.0 (C-10), 125.5 (C-11), 135.2 (C-11a), 130.0 (C-11b), 104.0 (C-11c), 114.5 (C-1′), 119.3 (C-2′), 122.4 (C-3′), 148.7 (C-4′), 105.8 (C-5′), 108.8 (C-6′), 12.8 (CH3), 18.8 (3CH3), 26.0 (C(CH3)3). MS, m/z (%) = 1347 (70), 1231 (2), 827 (4), 726 (100), 663 (17), 325 (100). Anal. Calcd for C26H26N2O5S (478.56): C, 65.25; H, 5.48; N, 5.85; S, 6.70. Found: C, 65.23; H, 5.51; N, 5.84; S, 6.72.

Cyclic voltammetry

Voltammetric measurements were carried out using a µ-Autolab (Ecochemie, Holland) controlled by the GPES electrochemical software. The working electrode was a glassy carbon electrode (0.3 mm diameter) properly polished using alumina paste prior to experiments. A Platinum gauze and a Ag/AgCl (3 M KCl) were used as counter and reference electrodes, respectively. Cyclic voltammograms were obtained with a scan rate of 50 mV s−1. Experiments were carried out at room temperature and in the presence of 0.1 M KCl or 0.02 M H2SO4 as supporting electrolyte, unless otherwise stated.

Biological assay

Bacterial strains and culture media

The studied microorganisms were both reference (from the American Type Culture Collection) and clinical (from Institut Pasteur and Ecole Nationale Vétérinaire d’Alford, France) strains of Providencia stuartii, Escherichia coli, Pseudomonas aeruginosa, Enterobacter aerogenes, Klebsiella pneumoniae, Candida albicans, Crytococcus neoformans and Trichophyton terrestre. Also, included were two clinical isolates of Trichophyton ajeloi and Trichophyton violaceum, obtained at the Laboratory of Microbiology and Antimicrobial Substances, University of Dschang and two clinical isolates of Candida parapsilosis and Staphylococcus aureus collected from Pasteur Centre (Yaounde-Cameroon). The bacterial and fungal species were grown at 37/28 °C and maintained on nutrient agar (NA, Conda, Madrid, Spain) and Sabouraud Dextrose Agar (SDA, Conda) slants respectively.

Preparation of microbial inoculum

The inocula of yeasts and bacteria were prepared from overnight cultures by picking numerous colonies and suspending them in sterile saline (NaCl) solution (0.90%). Absorbance was red at 530 nm for yeasts or at 600 nm for bacteria. Adjustment was done with a saline solution to match that of a 0.50 McFarland standard solution. From the prepared microbial solutions, other dilutions with saline solution were prepared to give a final concentration of 106 yeast cells/ml and 106 CFU/ml for bacteria [19, 26].

Conidia suspensions of dermatophyte species were prepared from 10 days old cultures respectively. The number of conidia was determined using a spectrophotometer and adjusted with sterile saline (NaCl) solution (0.90%) to an absorbance of 0.600 at 450 nm corresponding to a final concentration of about 1 × 105 spores/ml [27].

Antimicrobial activity

The antimicrobial activity was investigated by determining the minimum inhibitory concentrations (MICs), minimum bactericidal concentrations (MBC) and minimum fungicidal concentrations (MFCs).

MICs were determined by broth micro dilution [28, 29]. Stock solutions of the pure compounds were prepared in 10% v/v aqueous dimethylsulfoxide (DMSO) solution (Fisher chemicals, Strasbourg, France) at concentration of 1024 µg/ml. This was twofold serially diluted in Mueller-Hinton Broth (MHB) for bacteria and Sabouraud Dextrose Broth (SDB) for fungi to obtain a concentration range of 512–0.25 µg/ml. For every experiment, a sterility check (10% aqueous DMSO and medium), negative control (10% aqueous DMSO, medium and inoculum) and positive control (10% aqueous DMSO, medium, inoculum and water-soluble antibiotics) were included. One hundred microliters of each concentration was introduced into a well (96-wells microplate) containing 90 µl of SDB or MHB and 10 µl of inoculum was added to obtain a final concentration range of 256–0.125 µg/ml. The plates were covered with a sterile lid, and incubated on the shaker at 37 °C for 24 h (bacteria), 48 h (yeasts) or 5 days (dermatophytes). MICs were assessed visually after the corresponding incubation period and were taken as the lowest sample concentration at which there was no growth or virtually no growth. The assay was repeated thrice.

For the minimum microbicidal concentration (MMC) determination, 10 µl aliquots from each well that showed no growth of microorganism were plated on Mueller-Hinton Agar or Sabouraud Dextrose Agar and incubated at 37 °C for 24 h (bacteria), 48 h (yeasts) and at 28 °C for 10 days (dermatophytes). The lowest concentration that yielded no growth after the sub-culturing was taken as the MBCs or MFCs. Ciprofloxacin (Sigma-Aldrich, Steinheim, Germany) for bacteria, nystatin (Sigma-Aldrich, Steinheim, Germany) for yeasts and griseofulvin (Sigma-Aldrich, Steinheim, Germany) for dermatophytes were used as positive controls.

Results and discussion

Chemistry

The first step in the preparation of the coupling components was the synthesis of the relevant 2-aminothiophene 4 using the Gewald reaction [30, 31]. The synthesis of the thienocoumarins 4 from the multicomponent condensation of ketones, cyanoacetate and elemental sulphur was originally published early (Scheme 1) [25].
Figure 1
Scheme 1

Reactions’ sequences to compounds 7

Compound 4 was diazotized using nitrosyl sulphuric acid in the cold and coupled with the phenolic compounds 6a–e to yield the azo dyes 7a–e (Scheme 1 and Fig. 1) as previously described [24].
Figure 1
Fig. 1

Structures of the reactions’ products 7

Redox behaviors of the azo dyes

Compound 7a

Two distinct reduction peaks (Ic and IIc) were observed for the electroreduction of azo dyes 7a, the first one Ic at 0.0046 mv due to the cleavage of the azo group, –N=N– to give the reductive amines products I and II (Scheme 2). The second peak IIc at 0.3 mv, due to the reduction of C=O group of the intermediate I to CH2OH in product III (Scheme 2). Since the –N=N– group is more susceptible to reduction than the C=O groups, –N=N– group is reduced at less negative potential than other sites [32].
Figure 2
Scheme 2

Reduction and oxidation mechanisms of compound 7a and subsequent intermediates

The highly reactive intermediate product II provide quasi reversible oxidation–reduction peaks (Fig. 2) during reverse and subsequent forward scans due to the formation of oxidation product, 1,2-naphthaquinone IV and its subsequent reduction to dihydroxynaphthalene V (Scheme 2).
Figure 2
Fig. 2

Cyclic voltammogram of 1.2 × 10−3M 7a in 0.02 M sulfuric acid

Compound 7b

In the cyclic voltammograms of 7b (Fig. 3), four peaks were recorded, of which three cathodic peaks (Ic, IIc and IIIc) in the forward scan and one anodic peak (Ia) in the reverse scan, indicating the quasi-reversible electrochemical nature of the dye (Fig. 3). The anodic peak only appeared in the subsequent scan after the reduction step. Hence, this peak was obviously due to the corresponding oxidation of the reduction products. As reported in previous literatures [33], azo dyes with a hydroxyl group adjacent to an azo bridge can be reduced to yield the corresponding amine, which is most likely to be reoxidized in the return scan. The first peak (− 0.045 V) can be therefore attributed to the reduction of the –N=N– bridge adjacent to the hydroxyl group (Scheme 3).
Figure 3
Fig. 3

Cyclic voltammogram of 2 × 10−3M 7b in 0.02 M sulfuric acid

Figure 3
Scheme 3

Reduction and oxidation mechanisms of compound 7b and subsequent intermediates

The second peak (0.27 V) can therefore be attributed to the reduction of the second –N=N– bridge of compound A. The last peak (0.936 V) may be attributed to the catalytic hydrogen reduction of the carbonyl group (C=O) of the intermediate B to give compound E (scheme 3). The highly reactive intermediate product E provides a quasi reversible oxidation–reduction peaks (− 0.045 V) during reverse and subsequent forward scans (scheme 3).

Compound 7c

To understand the electrochemical behavior of dye 7c, the CV studies were carried out using solution with and without dye taking Ag wire as working electrode (Fig. 4). The potential scan used for the study was − 0.5–1.0 V. The dye solution, both showed single anodic peak approximately at − 0.0526 V and also one cathodic peak at approximately 0.168 V. The voltammetric curve of compound 7c showed that the reduction takes place in one step and one irreversible cathodic wave was observed in cyclic voltammogram (Fig. 4).
Figure 4
Fig. 4

Cyclic voltammogram of 2 × 10−3M 7c in 0.02 M sulfuric acid

The anodic peak is due to the reduction of compound 7c to compounds B and C through the intermediate A. The first step of the reduction process does not however require external supply of protons, because the starting reagent 7c is pre-protonated by the sulfuric acid crystallites. The clivage of the three azo bridges in the second step of the reduction requires six protons to yield compounds B and C. Intermediate B subsequently undergoes a quasi-reversible oxidation–reduction process during reverse and subsequent forward scans. The probable mechanism for the reduction process is displayed in scheme 4.
Figure 4
Scheme 4

Reduction and oxidation mechanisms of compound 7c and subsequent intermediates

Compound 7e

The voltammetric behavior of compound 7e was studied (Fig. 5). The single cathodic wave observed on the voltammograms of 7e apparently corresponds to the reduction of the azo group and appeared in the range 0.4–0.6 mV.
Figure 5
Fig. 5

Cyclic voltammograms of 2 × 10−3M 7e in 0.02 M sulfuric acid

The reduction process results in the clivage of the azo bridge leading to the formation of compounds I and II (Scheme 5). The intermediate II, further undergoes oxidation to afford compound III which in turn is reduced to give compound IV during reverse and subsequent forward scan.
Figure 5
Scheme 5

Reduction and oxidation mechanisms of compound 7e and subsequent intermediates

Antimicrobial activity

The azo compounds 7a–e and the entire precursors 1–4 and 6a–e were examined in vitro against bacterial and fungal species and the results are depicted in Table 1. All the compounds showed different degree of antimicrobial activities against the tested fungal and bacterial pathogens. Enterobacter aerogenes and E. coli were the most sensitive microorganisms while Trichophyton terrestre and Trichophyton violaceum were the most resistant. In general, bacterial species were more sensitive than fungal species; this can be due to the structural complexity of fungi compared with that of bacteria.
Table 1

Minimum Inhibitory Concentrations (MIC) and Minimum Microbicidal Concentrations (MMC) (µg/ml) of azo compounds and their entire precursors against fungal and bacterial strains

Microorganisms

Inhibition parameters

3

4

6a

6b

6c

6d

6e

7a

7b

7c

7d

7e

Reference drugsa

Providencia stuartii ATCC29916

MIC

> 256

> 256

128

> 256

> 256

64

> 256

16

256

32

128

32

2

MBC

nd

nd

> 256

nd

nd

256

nd

32

> 256

64

256

32

2

MBC/MIC

nd

nd

nd

nd

nd

8

nd

2

nd

2

2

1

1

Escherichia coli ATCC10536

MIC

32

128

128

32

32

64

64

4

32

32

16

16

8

MBC

128

256

256

128

128

128

128

8

> 256

128

64

64

8

MBC/MIC

4

2

2

4

4

2

2

2

nd

4

4

4

1

Enterobacter aerogenes ATCC13048

MIC

32

128

128

32

128

128

128

8

128

32

32

16

4

MBC

128

256

256

64

128

128

> 256

8

> 256

64

128

64

4

MBC/MIC

4

2

2

2

1

1

nd

1

nd

2

4

4

1

Pseudomonas aeruginosa ATCC27853

MIC

64

256

256

64

256

64

128

16

256

32

128

16

2

MBC

128

> 256

256

128

256

64

256

32

> 256

128

256

32

2

MBC/MIC

2

nd

1

2

1

1

2

2

nd

4

2

2

1

Klebsiella pneumoniae ATCC11296

MIC

128

256

128

128

> 256

64

> 256

16

> 256

32

256

16

4

MBC

256

> 256

256

256

nd

128

nd

32

nd

128

> 256

32

4

MBC/MIC

2

nd

2

2

nd

2

nd

2

nd

4

nd

2

1

Staphylococcus aureus

MIC

256

256

256

256

64

64

256

16

128

32

64

32

4

MBC

256

> 256

> 256

256

256

64

> 256

64

> 256

128

256

64

4

MBC/MIC

1

nd

nd

1

4

1

nd

4

nd

4

4

2

1

Trichophyton terrestre E1501

MIC

256

> 256

> 256

> 256

> 256

128

> 256

16

> 256

32

256

16

4

MFC

> 256

nd

nd

nd

nd

256

nd

16

nd

64

256

64

8

MFC/MIC

nd

nd

nd

nd

nd

2

nd

1

nd

2

1

4

2

Trichophyton violaceum

MIC

> 256

> 256

128

> 256

> 256

64

> 256

8

> 256

64

128

32

4

MFC

nd

nd

256

nd

nd

256

nd

16

nd

128

256

128

8

MFC/MIC

nd

nd

2

nd

nd

4

nd

2

nd

2

2

4

2

Trichophyton ajeloi

MIC

256

> 256

16

256

> 256

128

256

8

256

32

128

32

4

MFC

256

nd

64

256

nd

256

> 256

8

> 256

64

256

128

4

MFC/MIC

1

nd

4

1

nd

2

nd

1

nd

2

2

4

1

Candida parapsilosis ATCC22019

MIC

64

> 256

128

> 256

> 256

128

> 256

4

64

16

64

16

2

MFC

128

nd

128

nd

nd

> 256

nd

8

128

32

64

32

2

MFC/MIC

2

nd

1

nd

nd

nd

nd

2

2

2

1

2

1

Candida albicans ATCC9002

MIC

128

> 256

> 256

> 256

> 256

128

> 256

4

64

16

64

16

4

MFC

128

nd

nd

nd

nd

> 256

nd

8

128

32

64

64

4

MFC/MIC

1

nd

nd

nd

nd

nd

nd

2

2

2

1

4

1

Cryptococcus neoformans IP95026

MIC

32

> 256

32

> 256

> 256

128

> 256

2

256

16

32

8

4

MFC

64

nd

64

nd

nd

256

nd

2

> 256

32

64

16

4

MFC/MIC

2

nd

2

nd

nd

2

nd

1

nd

2

2

2

1

aCiprofloxacin for bacteria, Griseofulvin for dermatophytes and Nystatin for yeasts; nd : not determined; compounds 1 and 2 were not active against all the tested microorganisms at concentrations up to 256 µg/ml

No activity was noted with compounds 1 and 2 against all the tested microorganisms (not shown). However, the Knoevenagel condensation [34] of 1 and 2 afforded the coumarin intermediate 3 which exhibited a relatively higher antimicrobial activity. Moreover, diazotisation of compound 4 with nitrosyl sulphuric acid and coupling with phenol derivatives resulted into an effective enhancement of the antimicrobial activity in compounds 7a,c–e. Compounds 6a–e and 7a–e showed selective activities; their inhibitory effects being noted respectively on 10/12 (83.33%), 6/12 (50.00%), 4/12 (33.33%), 12/12 (100.00%), 5/12 (41.66%) and 12/12 (100%), 9/12 (75.00%), 12/12 (100%), 12/12 (100.00%), 12/12 (100%) of the studied microorganisms. Compounds 6d and 7a,c–e showed antimicrobial properties against all the tested microorganisms (MIC = 2–256 µg/ml). This finding suggests the antibacterial and antifungal potencies of these compounds. The lowest MIC value for these tested compounds (2 µg/ml) was obtained with compound 7a on Cryptococcus neoformans. The antimicrobial activities of compound 7a (MIC = 2–16 µg/ml) were in some cases equal or more important than those of ciprofloxacin (MIC = 2–8 µg/ml) and nystatin (MIC = 2–4 µg/ml) used as reference drugs; highlighting its good antimicrobial potency. The results of the MMC values indicate that most of them are not more than fourfold their corresponding MICs. This proves that the killing effects of many tested compounds could be expected on the most sensitive strains [35].

The present study highlighted the antimicrobial activity of the azo compounds and their precursors against the microorganisms including bacterial and fungal species. Although azo compounds have been reported to possess interesting activity against a wide range of microorganisms [3537], no study has hitherto been reported on the activity of the azo dyes 7a–e and their precursors 3, 4 and 6a–e against these types of pathogenic strains. As far as the structure–activity relationship is concerned, some structural features that might have influenced the antimicrobial activity of these azo compounds can be drawn from the comparison of the chemical structures of the screened compounds with different activities. Compound 7a was the most active azo compound, followed by 7e, 7c, 7d and 7b. It appears that, in general, hydroxyl, 2-tertbutyl, 4-methoxy and aromatic groups play a greater role in increasing the antimicrobial activity based on the substitution patterns of the aromatic rings.

Effects of azo functionality to the activity of compounds 7

It results from Table 1 that the microbicidal activity of compound 7c on P. stuartii ATCC29916, Klebsiella pneumoniae ATCC11296, Trichophyton terrestre E1501, Trichophyton violaceum, Trichophyton ajeloi, Candida parapsilosis, Candida albicans ATCC 9002 and Cryptococcus neoformans IP95026 is entirely due to the presence of azo groups in the molecule. The microbicidal activity of compound 7e on Providencia stuartii ATCC29916, Klebsiella pneumoniae ATCC11296, Staphylococcus aureus, Trichophyton terrestre E1501, Trichophyton violaceum, Trichophyton ajeloi, Candida parapsilosis, Candida albicans ATCC 9002, Candida parapsilosis ATCC 22019 and Cryptococcus neoformans IP95026 is also attributed to the presence of the azo function in the molecule. Conversely, it was noted that the azo functionality inhibited the activity on E. coli ATCC10536 and Enterobacter aerogenes ATCC13048 with the transformation of the starting materials 4 and 6b into compound 7b. These observations corroborate previous reports related to the role played by the azo function in similar biological active substances [38].

Conclusion

Thienylazoaryls compounds 7a–e were synthesized, studied electrochemically at a glassy carbon electrode and preliminarily evaluated for their in vitro antimicrobial properties. The reduction of the azo group in compounds 7 exhibited different behavior due to the constitutional structure of the dyes. It was observed that pre-protonated forms get involved in the reduction step and a different number of protons are involved. The protonation reaction was facilitated owing to the increasing electron density of the azo group, due to the donating effect of the hydroxyl group at the ortho position. Then, a decrease in the electron density on electroactive functional group led to an easy reduction process. Compounds 7a,c–e as well as their precursors 3 and 6d displayed good antibacterial and antifungal activities. The presence of hydroxyl, 2-tertbutyl, 4-methoxy and aromatic groups could explain their good antibacterial and antifungal activities. Further studies are needed to determine additional physicochemical and biological parameters in order to provide a deeper insight into the structure–activity relationship and to optimize the potentials of these compounds.

Abbreviations

T.L.C: 

thin layer chromatography

IR: 

infra-red

UV: 

ultra-violet

HREIMS: 

high resolution electron impact mass spectrometry

1H-NMR: 

proton nuclear magnetic resonance

13C-NMR: 

thirteen carbon nuclear magnetic resonance

DMSO: 

dimethylsulfoxide

TMS: 

tetramethylsilane

mp: 

melting points

THF: 

tetrahydrofuran

MIC: 

minimum inhibitory concentration

MBC: 

minimum bactericidal concentration

MFC: 

minimum fungicidal concentration

MHB: 

Mueller-Hinton Broth

SDB: 

sabouraud dextrose broth

MMC: 

minimum microbicidal concentration

CV: 

cyclic voltammogram

Declarations

Authors’ contributions

All authors equally contributed to the paper and have given approval to the final version of the paper. All authors read and approved the final manuscript.

Acknowledgements

ESF gratefully acknowledges financial support from DAAD (Grant No A/09/07421) for a scholarship. ADN is grateful to his supervisors Prof. Dr. J. S. Glaser and Dr. R. Marx for helpful suggestions in performing the NMR experiments. The necessary NMR spectrometers were provided by the Bavarian NMR Center (Bayerisches NMR-Zentrum). Additional financial supports for the work were obtained from the University of Dschang research grant committee and the Cameroonian Ministry of Higher Education special research allocation.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

With the authors.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Laboratory of Applied Synthetic Organic Chemistry, Department of Chemistry, Faculty of Science, University of Dschang, Dschang, Republic of Cameroon
(2)
Department of Organic Chemistry, University of Yaounde I, Yaounde, Republic of Cameroon
(3)
Laboratory of Microbiology and Antimicrobial Substances, Department of Biochemistry, Faculty of Science, University of Dschang, Dschang, Republic of Cameroon
(4)
Laboratory of Analytical and Molecular Chemistry, Faculty Polydisciplinaire of Safi, University Cadi Ayyad Marrakech, Safi, Morocco

References

  1. Filarowski A (2010) Perkin’s mauve: the history of the chemistry. Resonance 15(9):850–855View ArticleGoogle Scholar
  2. Bae JS, Freeman HS (2007) Aquatic toxicity evaluation of new direct dyes to the Daphnia magna. Dyes Pigm 73(1):81–85View ArticleGoogle Scholar
  3. Elisangela F, Andrea Z, Fabio DG, Cristiano RM, Regina DL, Artur CP (2009) Biodegradation of textile azo dyes by a facultative Staphylococcus arlettae strain VN-11 using a sequential microaerophilic/aerobic process. Int Biodeter Biodegrad 63:280–288View ArticleGoogle Scholar
  4. Rathod KM, Thakre NS (2013) Synthesis and antimicrobial activity of azo compounds containing m-cresol moiety. Chem Sci Trans 2(1):25–28View ArticleGoogle Scholar
  5. Gaffer HE, Fouda MMG, Khalifa ME (2016) Synthesis of some novel 2-amino-5-arylazothiazole disperse dyes for dyeing polyester fabrics and their antimicrobial activity. Molecules 21:122–131View ArticleGoogle Scholar
  6. Bae JS, Freeman HS, El-Shafei A (2003) Metallization of non-genotoxic direct dyes. Dyes Pigm 57(2):121–129View ArticleGoogle Scholar
  7. Garg HG, Praksh C (1972) Preparation of 4-arylazo-3,5-disubstituted-(2H)-1,2,6-thiadiazine 1,1-dioxides. J Med Chem 15(4):435–436View ArticleGoogle Scholar
  8. Węglarz-Tomczak E, Górecki Ł (2012) Azo dyes—biological activity and synthetic strategy. CHEMIK 66(12):1298–1307Google Scholar
  9. Menek N, Turgut G, Mustafa O (1999) Electrochemical behaviour of hexa[4-(phenylazo)phenoxy] cyclotriphasphazene. Turk J Chem 23:423–427Google Scholar
  10. Khazaal FA, Mohammed HJ (2016) Novel electrochemical behavior of 3-(5-(3-Methyl-1-phenylpyrazolazo)-1-nitroso-2-naphthol and use it for spectrophotometric determination of iron(III) in blood samples. Der Pharma Chemica 8(13):123–132Google Scholar
  11. Goyal RN, Verma MS, Singhal NK (1998) Voltammetric investigations of the reduction of direct orange-31 a bisazo dye. Croat Chem Acta 3:715–726Google Scholar
  12. Fox MR, Sumner HH (1986) The dyeing of cellulose fibers. Dyer’s Company Publication Trust, Bradford, p 149–159Google Scholar
  13. Shaikh A, Meshram JS (2015) Design, synthesis and pharmacological assay of novel azo derivatives of dihydropyrimidinones. Cogent Chemistry 1(1019809):1–9Google Scholar
  14. Sabnis RW (2016) The Gewald reaction in dye chemistry. Colora Technol 132:49–82View ArticleGoogle Scholar
  15. Khedr AM, Gaber M, Abd El-Zaher EH (2011) Synthesis, structural characterization, and antimicrobial activities of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes of triazole-based azodyes. Chin J Chem 29:1124–1132View ArticleGoogle Scholar
  16. Jain R, Sharma N, Radhapyari K (2009) Removal of hazardous azo dyes, metanil yellow from industrial wastewater using electrochemical technique. Eur Water 27(28):43–52Google Scholar
  17. Kariyajjanavar P, Narayana J, Nayaka YA, Umanaik M (2010) Electrochemical degradation and cyclic voltammetric studies of textile reactive azo dye cibacron navy WB. Portugaliae Electrochimica Acta 28(4):265–277View ArticleGoogle Scholar
  18. Fondjo ES, Djeukoua DKS, Tamokou J-D-D, Tsemeugne J, Kouamo S, Ngouanet D, Chouna JR, Nkeng-Efouet-Alango P, Kuiate J-R, Ngongang NA, Sondengam BL (2016) Synthesis, characterization, antimicrobial and antioxidant activities of the homocyclotrimer of 4-oxo-4 h-thieno[3,4-C]chromene-3-diazonium sulfate. Open Med Chem J 10:21–32View ArticleGoogle Scholar
  19. Tamokou J-D-D, Tsemeugne J, Sopbué FE, Sarkar P, Kuiate J-R, Djintchui AN, Sondengam BL, Bag PK (2016) Antibacterial and cytotoxic activities and SAR of some azo compounds containing thiophene backbone. Pharmacologia 7(4):182–192View ArticleGoogle Scholar
  20. Sahu DK, Ghosh G, Sahoo J, Kumar PS (2013) Evaluation of antimicrobial activity of some newly synthesized azo compounds derived from thiobarbituric acid. Int J Adv Chem Sci Appl 1(1):25–27Google Scholar
  21. Sopbué FE, Tsemeugne J, Tamokou J-D-D, Djintchui AN, Kuiaté J-R, Sondengam BL (2013) Synthesis and antimicrobial activities of some novel thiophene containing azo compounds. Heterocycl Commun 19:253–259Google Scholar
  22. Al-Mousawi SM, El-Apasery MA, Mahmoud HM (2013) Disperse Dyes based on aminothiophenes: their dyeing applications on polyester fabrics and their antimicrobial activity. Molecules 18:7081–7092View ArticleGoogle Scholar
  23. Ono M, Wada Y, Wu Y, Nemori R, Jinbo Y, Wang H, Lo KM, Yamaguchi N, Brunkhorst B, Otomo H, Wesolowski J, Way JC, Itoh I, Gillies S, Chen LB (1997) FP-21399 blocks HIV envelope protein-mediated membrane fusion and concentrates in lymph nodes. Nat Biotechnol 15(4):343–348View ArticleGoogle Scholar
  24. Tsemeugne J, Fondjo SE, Ngongang AD, Sabnis RW, Sondengam BL (2017) Coupling of the diazonium sulphate of 3-amino-4H-benzo[f]thieno[3,4-c](2H)chromen-4-one with phenol and naphthol derivatives in varied stoichiometries. Trends Org Chem 18:55–69Google Scholar
  25. Fondjo SE, Döpp D, Henkel G (2006) Reactions of some annelated 2-aminothiophenes with electron poor acetylenes. Tetrahedron 62:7121–7131View ArticleGoogle Scholar
  26. National Committee for Clinical Laboratory Standards (1992) Reference method for broth dilution antifungal susceptibility testing of yeast; approved standard, 2nd (eds) M27-A2. NCCLS, WayneGoogle Scholar
  27. Venugopal PV, Venugopal TV (1992) In vitro susceptibility of dermatophytes to imidazoles. Indian J Dermatol 37:34–35Google Scholar
  28. Nyaa TB, Tapondjou AL, Barboni L, Tamokou JD, Kuiate JR, Tane P, Park H (2009) NMR assignment and antimicrobial/antioxidant activities of 1β-hydroxyeuscaphic acid from the seeds of Butyrospermum parkii. J Nat Prod Sci 15:76–82Google Scholar
  29. Fogue SP, Lunga KP, Sopbue FE, Tamokou JD, Thaddée B, Tsemeugne J, Tienga TA, Kuiate JR (2012) Substituted 2-aminothiophenes: antifungal activities and effect on Microsporum gypseum protein profile. Mycoses Diagn Ther Prophyl Fungal Dis 55:310–317Google Scholar
  30. Gewald K (1961) Zur Reaktion von α-Oxo-mercaptanen mit Nitrilen. Angew Chem 73(3):114–115View ArticleGoogle Scholar
  31. Gewald K (1965) Heterocycles from CH acidic nitriles. VIII. 2-aminothiophene from α-oxo mercaptans and methylene-active nitriles. Chem Ber 98:3571–3577View ArticleGoogle Scholar
  32. Semiha Ç, Ender B, Mustafa O, Çiğdem A (2005) Electrochemical and spectroscopic study of 4-(Phenyldiazenyl)-2-{[tris(hydroxymethyl)methyl] amino- methylene}cyclohexa-3,5-dien-1(2H)-one mechanism of the azo and imine electroreduction. J Braz Chem Soc 16(4):711–717View ArticleGoogle Scholar
  33. Jiefei Y, Jinping J, Zifeng M (2004) Comparison of electrochemical behavior of hydroxyl-substituted and nonhydroxyl-substituted azo dyes at a glassy carbon electrode. J Chin Chem Soc 51:1319–1324View ArticleGoogle Scholar
  34. Knoevenagel E (1896) Über eine Darstellungsweise des Benzylidenacetessigesters. Ber Dtshe Chem Ges 29:172–174View ArticleGoogle Scholar
  35. Tamokou JD, Mpetga Simo DJ, Lunga PK, Tene M, Tane P, Kuiate JR (2012) Antioxidant and antimicrobial activities of ethyl acetate extract, fractions and compounds from the stem bark of Albizia adianthifolia (Mimosoideae). BMC Complement Altern Med 12(99):1–10Google Scholar
  36. Awad IM, Aly AA, Abdel AMA, Abdel ARA, Ahmed SH (1998) Synthesis of some 5-azo-(4′-substituted benzene-sulphamoyl)-8-hydroxyquinolines with antidotal and antibacterial activities. J Inorg Biochem 33(2):77–89View ArticleGoogle Scholar
  37. Samadhiya S, Halve H (2001) Synthetic utility of schiff bases as potential herbicidal agends. Orient J Chem 17:119–122Google Scholar
  38. Mkpenie V, Ebong G, Obot IB, Abasiekong B (2008) Evaluation of the effect of azo group on the biological activity of 1-(4-methylphenylazo)-2-naphthol. E J Chem 5:431–434View ArticleGoogle Scholar

Copyright

© The Author(s) 2017

Advertisement