How to cite this paper
Hassan, K., Shaban, E., ElHaddad, G., Sallam, A & Sayed, I. (2022). Synthesis, characterization, and antibacterial activity of azodyes incorporated acridine chromophore and their applications in polyester printing.Current Chemistry Letters, 11(1), 83-94.
Refrences
1 Mahmoud W.H., Sayed, F.N., Mohamed, G.G. (2016) Synthesis, characterization and in vitro antimicrobial and anti-breast cancer activity studies of metal complexes of novel pentadentate azo dye ligand. Appl. Organomet. Chem., 30 (11) 959-973.
2 Kantar C., Akal, H., Kaya, B., Islamoğlu, F., Türk, M., Şaşmaz, S. (2015) Novel phthalocyanines containing resorcinol azo dyes; synthesis, determination of pKa values, antioxidant, antibacterial and anticancer activity. J. Organomet. Chem., 783 28-39.
3 Ghasemi Z., Azizi, S., Salehi, R., Kafil, H.S. (2018) Synthesis of azo dyes possessing N-heterocycles and evaluation of their anticancer and antibacterial properties. Monatsh Chem Chem Mon., 149 (1) 149-157.
4 Saad F.A., El-Ghamry, H.A., Kassem, M.A., Khedr, A.M. (2019) Nano-synthesis, Biological Efficiency and DNA binding affinity of new homo-binuclear metal complexes with sulfa azo dye based ligand for further pharmaceutical applications. J Inorg Organomet Polym Mater., 29 (4) 1337-1348.
5 Muhammad‑Ali M.A., Hamza Salman, H., Jasim, E. (2019) Antioxidant ac tivity of some newly prepared symmetrically azodyes derived from sulfa drugs . Asian J. Pharm. Clin. Res., 12 (2) 479-483.
6 Gouda M.A., Eldien, H.F., Girges, M.M., Berghot, M.A. (2016) Synthesis and antitumor evaluation of thiophene based azo dyes incorporating pyrazolone moiety. J. Saudi Chem. Soc., 20 (2) 151-157.
7 Kennedy D.A., Vembu, N., Fronczek, F.R., Devocelle, M. (2011) Synthesis of mutual azo prodrugs of anti-inflammatory agents and peptides facilitated by α-aminoisobutyric acid. J. Org. Chem., 76 (23) 9641-7.
8 Wiley-VCH K.H. (2004) Industrial Dyes; Chemistry, Properties, Applications Edited by Klaus Hunger. Wiley-VCH: Weinheim. 2003. 660 pp. ISBN 3-527-30426-6. Org. Process Res. Dev., 8 (2) 296-297.
9 Benkhaya S., M'Rabet, S., El Harfi, A. (2020) Classifications, properties, recent synthesis and applications of azo dyes. Heliyon, 6 (1) e03271.
10 Finch C.A. (1986) Kirk-Othmer ‘Concise encyclopedia of chemical technology’. Edited by M. Grayson, Wiley-Interscience, New York, 1985. ISBN 0-471-86977-5. J.Br. Polym., 18 (6) 400.
11 Timpe H.J. (1991) Photochromism – molecules and systems. Herausgeber: Dürr, H., Bouas-Laurent, H. 1. Auflage, 1068 S. Amsterdam, Oxford, New York, Tokyo: Elsevier, Schriftenreihe: Studies in organic chemistry, 40. ISBN 0-444-87432-1. J. Prakt. Chem., 333 (5) 811-812.
12 Langhals H. (2004) Color Chemistry. Synthesis, Properties and Applications of Organic Dyes and Pigments. 3rd revised edition. By Heinrich Zollinger. Angew. Chem., Int. Ed., 43 (40) 5291-5292.
13 Chen R., Huo, L., Jaiswal, Y., Huang, J., Zhong, Z., Zhong, J., Williams, L., Xia, X., Liang, Y., Yan, Z. (2019) Design, Synthesis, Antimicrobial, and Anticancer Activities of Acridine Thiosemicarbazides Derivatives. Molecules, 24 (11) 2065.
14 Fu W., Li, X., Lu, X., Zhang, L., Li, R., Zhang, N., Liu, S., Yang, X., Wang, Y., Zhao, Y., et al. (2017) A novel acridine derivative, LS-1-10 inhibits autophagic degradation and triggers apoptosis in colon cancer cells. Cell Death Dis., 8 (10) e3086.
15 Wang N., Świtalska, M., Wang, L., Shaban, E., Hossain, M.I., El Sayed, I.E.T., Wietrzyk, J., Inokuchi, T. (2019) Structural Modifications of Nature-Inspired Indoloquinolines: A Mini review of their potential antiproliferative activity. Molecules, 24 (11) 2121.
16 Zadafiya S.K., Tailor, J.H., Malik, G.M. (2013) Disperse dyes based on thiazole, their dyeing application on polyester fiber and their antimicrobial activity. J. Chem., 851418.
17 Jasiński R., Miroslaw, B., Demchuk, O., Babyuk, D., Łapczuk-Krygier, A. (2016) In the search for experimental and quantumchemical evidence for zwitterionic nature of (2E)-3-[4-(dimethylamino)phenyl]-2-nitroprop-2-enenitrile - An extreme example of donor-π-acceptor push-pull molecule. J. Mol. Struct., 1108 689-697.
18 Ibrahim N.A., Abo-Shosha, M.H., El-Zairy, E.A.M.R., El-Zairy, E.M. (2006) New thickening agents for reactive printing of cellulosic fabrics. Carbohydr. Polym., 101 (6) 4430-4439.
19 Benkhaya S., M' rabet, S., El Harfi, A. (2020) A review on classifications, recent synthesis and applications of textile dyes. Inorg. Chem. Commun., 115 107891.
20 Ghorab M.M., Ragab, F.A., Heiba, H.I., El-Gazzar, M.G., Zahran, S.S. (2015) Synthesis, anticancer and radiosensitizing evaluation of some novel sulfonamide derivatives. Eur. J. Med. Chem., 92 682-692.
21 Molnar M., Harshad, B., Rastija, V., Pavić, V., Komar, M., Karnaš, M., Babic, J. (2018) Environmentally friendly approach to knoevenagel condensation of rhodanine in choline chloride: urea deep eutectic solvent and QSAR studies on their antioxidant activity. Molecules, 23 (8) 1897.
22 Karcı F. (2005) Synthesis of disazo dyes derived from heterocyclic components. Color. Technol., 121 (5) 275-280.
23 ISO 105-C06 Textiles: Tests for colour fastness. , in Part C06: Colour fastness to domestic and commercial laundering. 2010. p. 9.
24 ISO 105-X12 Textiles: Tests for colour fastness. Part X12: Colour fastness to rubbing. 2016. p. 5.
25 ISO 105-E04:Textiles -Tests for colour fastness- Part E04: Colour fastness to perspiration. 2013. p. 5.
26 ISO 105-P01:Textiles -Tests for colour fastness- Part P01: Colour fastness to dry heat (excluding pressing). 1993. p. 3.
27 ISO 105-B02:Textiles -Tests for colour fastness-Part B02: Colour fastness to artificial light: Xenon arc fading lamp test. 2013. p. 35.
28 Balouiri M., Sadiki, M., Ibnsouda, S.K. (2016) Methods for in vitro evaluating antimicrobial activity: A review. J. Pharm. Anal., 6 (2) 71-79.
29 Mohmed A., Fouda, A., Abdel-Rahman, M., Hassan, S., Gamal, S., Salah Salem, S., Shaheen, T.I. (2019) Fungal strain impacts the shape, bioactivity and multifunctional properties of green synthesized zinc oxide nanoparticle. Biocatal. Agric. Biotechnol., 19 101103.
30 Brown W.J. (1988) National Committee for Clinical Laboratory Standards agar dilution susceptibility testing of anaerobic gram-negative bacteria. Antimicrob Agents Chemother, 32 (3) 385.
31 Pfaller M.A., Burmeister, L., Bartlett, M.S., Rinaldi, M.G. (1988) Multicenter evaluation of four methods of yeast inoculum preparation. J Clin Microbiol, 26 (8) 1437-1441.
32 Kiehlbauch J.A., Hannett, G.E., Salfinger, M., Archinal, W., Monserrat, C., Carlyn, C. (2000) Use of the National Committee for Clinical Laboratory Standards guidelines for disk diffusion susceptibility testing in New York state laboratories. J Clin Microbiol, 38 (9) 3341-3348.
33 Fresco D., Coles, M., Heimberg, R.G., Liebowitz, M., Hami, S., Stein, M.B., Goetz, D. (2001) The liebowitz social anxiety scale: a comparison of the psychometric properties of self-report and clinician-administered formats. Psychol Med., 31(6) 1025-1035.
34 Laidlaw B. (1991) Standard methods for the determination of the colour fastness of textiles and leather, 5th edition (BS 1006:1990). J. Soc. Dye., 107 (2) 84.
35 Salami A.U., Kabir, Y.M., Ademola, B.K., Obinna, N.P., Ziyaei, H.A. (2020) Synthesis and dyeing performance of some amphiphilic naphthalimide azo disperse dyes on polyester fabrics. J. Serbian Chem. Soc., 85 (10) 1253-1264.
36 McLellan M.R., Lind, L.R., Kime, R.W. (1995) Hue angle determinations and statistical analysis for multiquadrant hunter L,a,b data. J. Food Qual., 18 (3) 235-240.
37 Rahman M.M., Haque, T.M.A., Sourav, N.S., Rahman, S., Yesmin, S., Mia, R., Al Noman, A., Begum, K. (2021) Synthesis and investigation of dyeing properties of 8-hydroxyquinoline-based azo dyes. J. Iran. Chem. Soc., 18 (4) 817-826.
38 Mahmoud Elkholy Y., Helmy Helal, M., wahba Erian, A. (2001) Novel synthesis of thiazole disperse dye derivatives. Pigm resin technol, 30 (3) 168-171.
39 Patel D.M., Patel, T.S., Dixit, B.C. (2013) Synthesis, characterization and dyeing performance of new bisazo–bisazomethine disperse dyes. J. Saudi Chem. Soc., 17 (2) 203-209.
40 Ketema A., Worku, A. (2020) Review on intermolecular forces between dyes used for polyester dyeing and polyester fiber. J. Chem., 7.
41 Al-Etaibi A.M., El-Apasery, M.A. (2020) A Comprehensive review on the synthesis and versatile Applications of biologically active pyridone-bBased disperse dyes. Int J Environ Res Public Health, 17 (13) 4714.
42 Otutu J.O., E.M, E., Ameru, S.U. (2014) Synthesis of disazo disperse dye compounds derived from 4- bromoaniline and 3-aminophenol as potential near infra-red absorbers. Chem. Mater., 6 (2) 40-46.
43 Salem S.S., Mohamed, A., El-Gamal, M., Talat, M., Fouda, A. (2019) Biological decolorization and degradation of azo dyes from textile wastewater effluent by aspergillus niger. EJCHEM., 62 (10) 1799-1813.
44 Alsharif S.M., Salem, S.S., Abdel-Rahman, M.A., Fouda, A., Eid, A.M., El-Din Hassan, S., Awad, M.A., Mohamed, A.A. (2020) Multifunctional properties of spherical silver nanoparticles fabricated by different microbial taxa. Heliyon, 6 (5) e03943.
45 Fouda A., Abdel-Maksoud, G., Abdel-Rahman, M.A., Eid, A.M., Barghoth, M.G., El-Sadany, M.A.-H. (2019) Monitoring the effect of biosynthesized nanoparticles against biodeterioration of cellulose-based materials by Aspergillus niger. Cellulose, 26 (11) 6583-6597.
2 Kantar C., Akal, H., Kaya, B., Islamoğlu, F., Türk, M., Şaşmaz, S. (2015) Novel phthalocyanines containing resorcinol azo dyes; synthesis, determination of pKa values, antioxidant, antibacterial and anticancer activity. J. Organomet. Chem., 783 28-39.
3 Ghasemi Z., Azizi, S., Salehi, R., Kafil, H.S. (2018) Synthesis of azo dyes possessing N-heterocycles and evaluation of their anticancer and antibacterial properties. Monatsh Chem Chem Mon., 149 (1) 149-157.
4 Saad F.A., El-Ghamry, H.A., Kassem, M.A., Khedr, A.M. (2019) Nano-synthesis, Biological Efficiency and DNA binding affinity of new homo-binuclear metal complexes with sulfa azo dye based ligand for further pharmaceutical applications. J Inorg Organomet Polym Mater., 29 (4) 1337-1348.
5 Muhammad‑Ali M.A., Hamza Salman, H., Jasim, E. (2019) Antioxidant ac tivity of some newly prepared symmetrically azodyes derived from sulfa drugs . Asian J. Pharm. Clin. Res., 12 (2) 479-483.
6 Gouda M.A., Eldien, H.F., Girges, M.M., Berghot, M.A. (2016) Synthesis and antitumor evaluation of thiophene based azo dyes incorporating pyrazolone moiety. J. Saudi Chem. Soc., 20 (2) 151-157.
7 Kennedy D.A., Vembu, N., Fronczek, F.R., Devocelle, M. (2011) Synthesis of mutual azo prodrugs of anti-inflammatory agents and peptides facilitated by α-aminoisobutyric acid. J. Org. Chem., 76 (23) 9641-7.
8 Wiley-VCH K.H. (2004) Industrial Dyes; Chemistry, Properties, Applications Edited by Klaus Hunger. Wiley-VCH: Weinheim. 2003. 660 pp. ISBN 3-527-30426-6. Org. Process Res. Dev., 8 (2) 296-297.
9 Benkhaya S., M'Rabet, S., El Harfi, A. (2020) Classifications, properties, recent synthesis and applications of azo dyes. Heliyon, 6 (1) e03271.
10 Finch C.A. (1986) Kirk-Othmer ‘Concise encyclopedia of chemical technology’. Edited by M. Grayson, Wiley-Interscience, New York, 1985. ISBN 0-471-86977-5. J.Br. Polym., 18 (6) 400.
11 Timpe H.J. (1991) Photochromism – molecules and systems. Herausgeber: Dürr, H., Bouas-Laurent, H. 1. Auflage, 1068 S. Amsterdam, Oxford, New York, Tokyo: Elsevier, Schriftenreihe: Studies in organic chemistry, 40. ISBN 0-444-87432-1. J. Prakt. Chem., 333 (5) 811-812.
12 Langhals H. (2004) Color Chemistry. Synthesis, Properties and Applications of Organic Dyes and Pigments. 3rd revised edition. By Heinrich Zollinger. Angew. Chem., Int. Ed., 43 (40) 5291-5292.
13 Chen R., Huo, L., Jaiswal, Y., Huang, J., Zhong, Z., Zhong, J., Williams, L., Xia, X., Liang, Y., Yan, Z. (2019) Design, Synthesis, Antimicrobial, and Anticancer Activities of Acridine Thiosemicarbazides Derivatives. Molecules, 24 (11) 2065.
14 Fu W., Li, X., Lu, X., Zhang, L., Li, R., Zhang, N., Liu, S., Yang, X., Wang, Y., Zhao, Y., et al. (2017) A novel acridine derivative, LS-1-10 inhibits autophagic degradation and triggers apoptosis in colon cancer cells. Cell Death Dis., 8 (10) e3086.
15 Wang N., Świtalska, M., Wang, L., Shaban, E., Hossain, M.I., El Sayed, I.E.T., Wietrzyk, J., Inokuchi, T. (2019) Structural Modifications of Nature-Inspired Indoloquinolines: A Mini review of their potential antiproliferative activity. Molecules, 24 (11) 2121.
16 Zadafiya S.K., Tailor, J.H., Malik, G.M. (2013) Disperse dyes based on thiazole, their dyeing application on polyester fiber and their antimicrobial activity. J. Chem., 851418.
17 Jasiński R., Miroslaw, B., Demchuk, O., Babyuk, D., Łapczuk-Krygier, A. (2016) In the search for experimental and quantumchemical evidence for zwitterionic nature of (2E)-3-[4-(dimethylamino)phenyl]-2-nitroprop-2-enenitrile - An extreme example of donor-π-acceptor push-pull molecule. J. Mol. Struct., 1108 689-697.
18 Ibrahim N.A., Abo-Shosha, M.H., El-Zairy, E.A.M.R., El-Zairy, E.M. (2006) New thickening agents for reactive printing of cellulosic fabrics. Carbohydr. Polym., 101 (6) 4430-4439.
19 Benkhaya S., M' rabet, S., El Harfi, A. (2020) A review on classifications, recent synthesis and applications of textile dyes. Inorg. Chem. Commun., 115 107891.
20 Ghorab M.M., Ragab, F.A., Heiba, H.I., El-Gazzar, M.G., Zahran, S.S. (2015) Synthesis, anticancer and radiosensitizing evaluation of some novel sulfonamide derivatives. Eur. J. Med. Chem., 92 682-692.
21 Molnar M., Harshad, B., Rastija, V., Pavić, V., Komar, M., Karnaš, M., Babic, J. (2018) Environmentally friendly approach to knoevenagel condensation of rhodanine in choline chloride: urea deep eutectic solvent and QSAR studies on their antioxidant activity. Molecules, 23 (8) 1897.
22 Karcı F. (2005) Synthesis of disazo dyes derived from heterocyclic components. Color. Technol., 121 (5) 275-280.
23 ISO 105-C06 Textiles: Tests for colour fastness. , in Part C06: Colour fastness to domestic and commercial laundering. 2010. p. 9.
24 ISO 105-X12 Textiles: Tests for colour fastness. Part X12: Colour fastness to rubbing. 2016. p. 5.
25 ISO 105-E04:Textiles -Tests for colour fastness- Part E04: Colour fastness to perspiration. 2013. p. 5.
26 ISO 105-P01:Textiles -Tests for colour fastness- Part P01: Colour fastness to dry heat (excluding pressing). 1993. p. 3.
27 ISO 105-B02:Textiles -Tests for colour fastness-Part B02: Colour fastness to artificial light: Xenon arc fading lamp test. 2013. p. 35.
28 Balouiri M., Sadiki, M., Ibnsouda, S.K. (2016) Methods for in vitro evaluating antimicrobial activity: A review. J. Pharm. Anal., 6 (2) 71-79.
29 Mohmed A., Fouda, A., Abdel-Rahman, M., Hassan, S., Gamal, S., Salah Salem, S., Shaheen, T.I. (2019) Fungal strain impacts the shape, bioactivity and multifunctional properties of green synthesized zinc oxide nanoparticle. Biocatal. Agric. Biotechnol., 19 101103.
30 Brown W.J. (1988) National Committee for Clinical Laboratory Standards agar dilution susceptibility testing of anaerobic gram-negative bacteria. Antimicrob Agents Chemother, 32 (3) 385.
31 Pfaller M.A., Burmeister, L., Bartlett, M.S., Rinaldi, M.G. (1988) Multicenter evaluation of four methods of yeast inoculum preparation. J Clin Microbiol, 26 (8) 1437-1441.
32 Kiehlbauch J.A., Hannett, G.E., Salfinger, M., Archinal, W., Monserrat, C., Carlyn, C. (2000) Use of the National Committee for Clinical Laboratory Standards guidelines for disk diffusion susceptibility testing in New York state laboratories. J Clin Microbiol, 38 (9) 3341-3348.
33 Fresco D., Coles, M., Heimberg, R.G., Liebowitz, M., Hami, S., Stein, M.B., Goetz, D. (2001) The liebowitz social anxiety scale: a comparison of the psychometric properties of self-report and clinician-administered formats. Psychol Med., 31(6) 1025-1035.
34 Laidlaw B. (1991) Standard methods for the determination of the colour fastness of textiles and leather, 5th edition (BS 1006:1990). J. Soc. Dye., 107 (2) 84.
35 Salami A.U., Kabir, Y.M., Ademola, B.K., Obinna, N.P., Ziyaei, H.A. (2020) Synthesis and dyeing performance of some amphiphilic naphthalimide azo disperse dyes on polyester fabrics. J. Serbian Chem. Soc., 85 (10) 1253-1264.
36 McLellan M.R., Lind, L.R., Kime, R.W. (1995) Hue angle determinations and statistical analysis for multiquadrant hunter L,a,b data. J. Food Qual., 18 (3) 235-240.
37 Rahman M.M., Haque, T.M.A., Sourav, N.S., Rahman, S., Yesmin, S., Mia, R., Al Noman, A., Begum, K. (2021) Synthesis and investigation of dyeing properties of 8-hydroxyquinoline-based azo dyes. J. Iran. Chem. Soc., 18 (4) 817-826.
38 Mahmoud Elkholy Y., Helmy Helal, M., wahba Erian, A. (2001) Novel synthesis of thiazole disperse dye derivatives. Pigm resin technol, 30 (3) 168-171.
39 Patel D.M., Patel, T.S., Dixit, B.C. (2013) Synthesis, characterization and dyeing performance of new bisazo–bisazomethine disperse dyes. J. Saudi Chem. Soc., 17 (2) 203-209.
40 Ketema A., Worku, A. (2020) Review on intermolecular forces between dyes used for polyester dyeing and polyester fiber. J. Chem., 7.
41 Al-Etaibi A.M., El-Apasery, M.A. (2020) A Comprehensive review on the synthesis and versatile Applications of biologically active pyridone-bBased disperse dyes. Int J Environ Res Public Health, 17 (13) 4714.
42 Otutu J.O., E.M, E., Ameru, S.U. (2014) Synthesis of disazo disperse dye compounds derived from 4- bromoaniline and 3-aminophenol as potential near infra-red absorbers. Chem. Mater., 6 (2) 40-46.
43 Salem S.S., Mohamed, A., El-Gamal, M., Talat, M., Fouda, A. (2019) Biological decolorization and degradation of azo dyes from textile wastewater effluent by aspergillus niger. EJCHEM., 62 (10) 1799-1813.
44 Alsharif S.M., Salem, S.S., Abdel-Rahman, M.A., Fouda, A., Eid, A.M., El-Din Hassan, S., Awad, M.A., Mohamed, A.A. (2020) Multifunctional properties of spherical silver nanoparticles fabricated by different microbial taxa. Heliyon, 6 (5) e03943.
45 Fouda A., Abdel-Maksoud, G., Abdel-Rahman, M.A., Eid, A.M., Barghoth, M.G., El-Sadany, M.A.-H. (2019) Monitoring the effect of biosynthesized nanoparticles against biodeterioration of cellulose-based materials by Aspergillus niger. Cellulose, 26 (11) 6583-6597.