PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Pyrazole-based photoinitiator with antibacterial activity

Treść / Zawartość
Identyfikatory
Warianty tytułu
PL
Fotoinicjator na bazie pirazolu o działaniu przeciwbakteryjnym
Języki publikacji
EN
Abstrakty
EN
1-(naphthalen-2-yl)-2-(1H-pyrazol-1-yl) ethanone (MPPY) was synthesized. The structure was characterized by spectral analysis (1H-NMR, FT-IR). The molar absorptivity of MPPY is high enough, similarly to acetonaphthone derivatives, to be used as an efficient type I photoinitiator. The influence of MPPY concentration and the addition of the co-initiator N-methyldiethanolamine (MDEA) on methyl methacrylate (MMA) polymerization were also investigated. Additionally, MPPY showed good antibacterial activity against Escherichia coli and Staphylococcus aureus (diffusion method).
PL
Zsyntetyzowano 1-(naftalen-2-ylo)-2-(1H-pirazol-1-ylo)etanon (MPPY). Strukturę scharakteryzowano metodą analizy spektralnej (1H-NMR, FT-IR). Molowa absorpcja MPPY jest na tyle wysoka, że można go stosować, podobnie jak pochodne acetonaftonu, jako skuteczny fotoinicjator typu I. Zbadano również wpływ stężenia MPPY oraz dodatku koinicjatora N-metylodietanoloaminy (MDEA) na polimeryzację metakrylanu metylu (MMA). Dodatkowo MPPY wykazywał aktywność przeciwbakteryjną w stosunku do Escherichia coli i Staphylococcus aureus (metoda dyfuzji).
Czasopismo
Rocznik
Strony
167--172
Opis fizyczny
Bibliogr. 36 poz., rys., tab., wykr.
Twórcy
  • Department of Chemistry, Faculty of Science and Letters, Yildiz Technical University, Davutpasa Campus, 34220 Istanbul, Turkey
  • Department of Chemistry, Faculty of Science and Letters, Yildiz Technical University, Davutpasa Campus, 34220 Istanbul, Turkey
Bibliografia
  • [1] Dietliker K.: “A compilation of photoinitiators commercially available for UV Today”, SITA Technology Limited, Edinburgh, London 2002.
  • [2] Davidson R.S.: “Exploring the Science, Technology and Applications of U.V. and E.B. Curing”, SITA Technology, London 1999.
  • [3] Dizman H.M., Arsu N.: Materials Today Communications 2023, 35, 105599. https://doi.org/10.1016/j.mtcomm.2023.105599
  • [4] Dumur F.: Polymers 2023, 15(21), 4202. https://doi.org/10.3390/polym15214202
  • [5] Yagci Y., Jockusch S., Turro N.J.: Macromolecules 2010, 43(15), 6245. https://doi.org/10.1021/ma1007545
  • [6] Bruder F.K., Hagen R., Rölle T. et al.: Angewandte Chemie International Edition 2011, 50(20), 4552. https://doi.org/10.1002/anie.201002085
  • [7] Dietlin C., Schweizer S., Xiao P. et al.: Polymer Chemistry 2015, 6, 3895. https://doi.org/10.1039/c5py00258c
  • [8] Esen D.S., Karasu F., Arsu N.: Progress in Organic Coatings 2011, 70(2-3), 102. https://doi.org/10.1016/j.porgcoat.2010.10.010
  • [9] Crivello J.V.: Nuclear Instruments and Methods in Physics Research B 1999, 151(1-4), 8. https://doi.org/10.1016/S0168-583X(99)00109-3
  • [10] Dumur F.: European Polymer Journal 2023, 187, 111883. https://doi.org/10.1016/j.eurpolymj.2023.111883
  • [11] Hammoud F., Pavlou A., Petropoulos A. et al.: Polymer Chemistry 2022, 13, 4817. https://doi.org/10.1039/D2PY00753C
  • [12] Crivello J.V., Dietliker K.: “Photoinitiators for Free Radical Cationic & Anionic Photopolymerization”, John Wiley and Sons, Chichester 1998.
  • [13] Green W.A.: “Industrial Photoinitiators: A Technical Guide”, CRC Press., Boca Raton 2010. https://doi.org/10.1201/9781439827468
  • [14] Aydın M., Arsu N., Yagci Y. et al.: Macromolecules 2005, 38(10), 4133. https://doi.org/10.1021/ma047560t
  • [15] Dogruyol S.K., Dogruyol Z., Kazancioglu E.O. et al.: European Polymer Journal 2023, 198, 112440. https://doi.org/10.1016/j.eurpolymj.2023.112440
  • [16] Fouassier J.P., Lalevee J.: “Photoinitiators for Polymer Synthesis: Scope, Reactivity and Efficiency”, Wiley- VCH, Weinheim 2012. https://doi.org/10.1002/9783527648245
  • [17] Segurola J., Allen N.S., Edge M. et al.: Progress in Organic Coatings 1999, 37(1-2), 23. https://doi.org/10.1016/S0300-9440(99)00052-1
  • [18] Jančovičová V., Kindernay J., Jakubíková Z. et al.: Chemical Papers 2007, 61(5), 383. https://doi.org/10.2478/s11696-007-0052-1
  • [19] Karrouchi K., Radi S., Ramli Y. et al.: Molecules 2018, 23(1), 134. https://doi.org/10.3390/molecules23010134
  • [20] Rosati O., Curini M., Marcotullio M.C. et al.: Bioorganic and Medicinal Chemistry 2007, 15(10), 3463. https://doi.org/10.1016/j.bmc.2007.03.006
  • [21] Szabo G., Fischer J., Kis-Varga A. et al.: Journal of Medicinal Chemistry 2008, 51, 142. https://doi.org/10.1021/jm070821f
  • [22] Benaamane N., Nedjar-Kolli B., Bentarzi Y. et al.: Bioorganic and Medicinal Chemistry 2008, 16(6), 3059. https://doi.org/10.1016/j.bmc.2007.12.033
  • [23] Keskin S., Arsu N.: Polymer Bulletin 2006, 57, 643. https://doi. org/10.1007/s00289-006-0620-5
  • [24] Keskin S., Arsu N.: Progress in Organic Coatings 2006, 57(4), 348. https://doi.org/10.1016/j.porgcoat.2006.09.014
  • [25] Dereli U., Cakmak B. H., Dogruyol S. K.: Journal of Photopolymer Science and Technology 2019, 32(6), 795. https://doi.org/10.2494/photopolymer.32.795
  • [26] Ozcan F., Dogruyol Z., Dogruyol S. K.: Polimery 2023, 68(4), 215. https://doi.org/10.14314/polimery.2023.4.3
  • [27] Birtane H., Şen F., Bozdağ B. et al.: Polymer Bulletin 2021, 78, 3588. https://doi.org/10.1007/s00289-020-03287-0
  • [28] Gokkaya D., Topuzogullari M., Arasoglu T. et al.: Polymer International 2021, 70(6), 836. https://doi.org/10.1002/pi.6170
  • [29] Yan J., Zeng B., Wang L. et al.: Photochemical and Photobiological Sciences 2020, 21, 1417. https://doi.org/10.1007/s43630-022-00231-1
  • [30] Perez R.M., Avila J.G., Perez S. et al.: Journal of Ethnopharmacology 1990, 29(1), 111. https://doi.org/10.1016/0378-8741(90)90104-2
  • [31] Decker C., Moussa K.: Macromolecules 1989, 22(12), 4455. https://doi.org/10.1021/ma00202a013
  • [32] Homocianu M., Airinei A., Dorohoi D.O. et al.: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2011, 82(1), 355. https://doi.org/10.1016/j.saa.2011.07.061
  • [33] Balta D.K., Temel G., Aydin M. et al.: European Polymer Journal 2010, 46(6), 1374. https://doi.org/10.1016/j.eurpolymj.2010.03.022
  • [34] Attar A., Yapaoz M.A: Preparative Biochemistry and Biotechnology 2018, 48(7), 629. https://doi.org/10.1080/10826068.2018.1479862
  • [35] Katwal R., Kaur H, Sharma G. et al.: Journal of Industrial and Engineering Chemistry 2015, 31, 173. https://doi.org/10.1016/j.jiec.2015.06.021
  • [36] Liu J.J, Zhao M., Zhang X. et al.: Mini Reviews in Medicinal Chemistry 2013, 13(13), 1966. https://doi.org/10.2174/13895575113139990078
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-3d69e62a-d95d-475b-9461-4bd71d77b49d
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.