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Please use this identifier to cite or link to this item: https://oldena.lpnu.ua/handle/ntb/55759
Title: Ionic Liquid-Functionalized Titanomagnetite Nanoparticles as Efficient and Recyclable Catalyst for Green Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones
Other Titles: Йонні рідкофункціоналізовані титаномагнетитні наночастинки як ефективний і відновлювальний каталізатор зеленого синтезу 2,3-дигідрохіназолін-4(1Н)-ону
Authors: Azarifar, Davood
Badalkhani, Omolbanin
Chehregosha, Morteza
Jaymand, Mehdi
Affiliation: Bu-Ali Sina University
Tabriz University of Medical Sciences
Bibliographic description (Ukraine): Ionic Liquid-Functionalized Titanomagnetite Nanoparticles as Efficient and Recyclable Catalyst for Green Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones / Davood Azarifar, Omolbanin Badalkhani, Morteza Chehregosha, Mehdi Jaymand // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 14. — No 1. — P. 62–69.
Bibliographic description (International): Ionic Liquid-Functionalized Titanomagnetite Nanoparticles as Efficient and Recyclable Catalyst for Green Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones / Davood Azarifar, Omolbanin Badalkhani, Morteza Chehregosha, Mehdi Jaymand // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 14. — No 1. — P. 62–69.
Is part of: Chemistry & Chemical Technology, 1 (14), 2020
Issue: 1
Issue Date: 24-Jan-2020
Publisher: Видавництво Львівської політехніки
Lviv Politechnic Publishing House
Place of the edition/event: Львів
Lviv
DOI: doi.org/10.23939/chcht14.01.062
Keywords: йонна рідина
наночастинки титаномагнетиту
нанокаталізатор
зелена хімія
органічний синтез
ionic liquid
titanomagnetite nanoparticles
nanocatalyst
green chemistry
organic synthesis
Number of pages: 8
Page range: 62-69
Start page: 62
End page: 69
Abstract: Методом ко-осадження синтезовано наночастинки титаномагнетиту (Fe3-xTixO4 NPs) та проведено їх функціоналізацію з використанням 3-триметоксилілпропілхлоридного силанового агента і аспарагінату тетрабутиламонію за допомогою нового однореакторного синтезу з метою одержання Fe3-xTixO4 NPs, модифікованих йонною рідиною. Встановлено, що синтезовані NPs є ефективним і відновлювальним нанокаталізатором однореакторного трикомпонентного синтезу 2,3-дигідрохіназолін-4(1H)-ону без використання розчинників. Показано, що легкість магнітної сепарації та ефективна відновлюваність каталізатора, високі виходи реакцій, малий час реакції, та відсутність розчинників є найважливішими перевагами нового методу. Синтезовані Fe3-xTixO4 NPs можна використовувати як нанокаталізатор у промисловості.
In the present study, titanomagnetite nanoparticles (Fe3-xTixO4 NPs) were synthesized via coprecipitation approach and then functionalized using 3- trimethoxysilylpropyl chloride silan coupling agent followed by tetrabutylammonium asparaginate through a facial and newly one-pot procedure to afford an ionic liquid (IL)-modified Fe3-xTixO4 NPs. The synthesized NPs were examined as potent and recyclable nanocatalysts for one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones under solvent-free conditions. Easy magnetic separation and efficient recyclability of the catalyst, excellent yields of the reactions, low reaction times as well as solvent-free conditions are the most important advantages of the present procedure that qualified the fabricated Fe3-xTixO4 NPs as a nanocatalyst for industrial applications.
URI: https://ena.lpnu.ua/handle/ntb/55759
Copyright owner: © Національний університет “Львівська політехніка”, 2020
© Azarifar D., Badalkhani O., Chehregosha M., Jaymand M., 2020
URL for reference material: https://doi.org/10.1039/c4gc00164h
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[3] Garrett C., Prasad K., Adv. Synth. Catal., 2004, 346, 889. https://doi.org/10.1002/adsc.200404071
[4] Lu A., Salabas E., Schth F., Angew. Chem. Int. Edit., 2007, 46, 1222. https://doi.org/10.1002/anie.200602866
[5] Polshettiwar V., Luque R., Fihri A. et al., Chem. Rev., 2011, 111, 3036. https://doi.org/10.1021/cr100230z
[6] Du Y., Yao F., Tuo Y., Cai M., J. Chem. Res., 2017, 41, 725. https://doi.org/10.3184/174751917X15122516000113
[7] Bell A., Science, 2003, 299, 1688. https://doi.org/10.1126/science.1083671
[8] Polshettiwar V., Varma R., Green Chem., 2010, 12, 743. https://doi.org/10.1039/b921171c
[9] Farnoudian-Habibi A., Massoumi B., Jaymand M., Spectrochim. Acta A, 2016, 168, 235. https://doi.org/10.1016/j.saa.2016.06.013
[10] Poorgholy N., Massoumi B., Jaymand M., Int. J. Biol. Macromol., 2017, 97, 654. https://doi.org/10.1016/j.ijbiomac.2017.01.063
[11] Muller R., Laurent S., Forge D. et al., Chem. Rev., 2008, 108, 2064. https://doi.org/10.1021/cr0306788
[12] Teja A., Koh P., Prog. Cryst. Growth Charact. Mater., 2009, 55, 22. https://doi.org/10.1016/j.pcrysgrow.2008.08.003
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[15] Bliem J., Pavelec J., Gamba O. et al., Phys Rev. B, 2015, 92, 075440. https://doi.org/10.1103/PhysRevB.92.075440
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[19] Rajesh U., Divya, Rawat D., RSC Adv., 2014, 4, 41323. https://doi.org/10.1039/P.4RA06803C
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[40] Mhaske S., Argade N., Tetrahedron, 2006, 62, 9787. https://doi.org/10.1016/j.tet.2006.07.098
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[42] Dabiri M., Salehi P., Baghbanzadeh M., Monatsh. Chem., 2007, 138, 1191. https://doi.org/10.1007/s00706-007-0635-0
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[45] Davoodnia A., Allameh S., Fakhari A., Tavakoli-Hoseini N., Chin. Chem. Lett., 2010, 21, 550. https://doi.org/10.1016/j.cclet.2010.01.032
[46] Esmaeilpour M., Javidi J., Zahmatkesh S., Fahimi N., Monatsh. Chem., 2017, 148, 947. https://doi.org/10.1007/s00706-016-1832-5
[47] Alinezhad H., Tajbakhsh M., Ghobati N., Res. Rev. Mater. Sci. Chem., 2014, 3, 123.
[48] Baghbanzadeh M., Salehi P., Dabiri M., Kozehgarya G., Synthesis, 2006, 2, 344. https://doi.org/10.1055/s-2005-924766
[49] Dabiri M., Salehi P., Otokesh S. et al., Tetrahedron Lett., 2005, 46, 6123. https://doi.org/10.1016/j.tetlet.2005.06.157
[50] Salehi P., Dabiri M., Baghbanzadeh M., Bahramnejad M., Synth. Commun., 2006, 36, 2287. https://doi.org/10.1080/00397910600639752
[51] Chen J., Wu D., He F. et al., Tetrahedron Lett., 2008, 49, 3814. https://doi.org/10.1016/j.tetlet.2008.03.127
[52] Salehi P., Dabiri M., Zolfigol M., Baghbanzadeh M., Synlett., 2005, 7, 1155. https://doi.org/10.1055/s-2005-865200
[53] Allen C., Richard P., Ward A. et al., Tetrahedron Lett., 2006, 47, 7367. https://doi.org/10.1016/j.tetlet.2006.08.007
[54] Azarifar D., Badalkhani O., Abbasi Y., Appl. Organomet. Chem., 2018, 32, e3949. https://doi.org/10.1002/aoc.3949
[55] Yang S., He H., Wu D. et al., Appl. Catal. B, 2009, 89, 527. https://doi.org/10.1016/j.apcatb.2009.01.012
[56] Su W., Yang B., Aust. J. Chem., 2002, 55, 695. https://doi.org/10.1071/CH02117
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Appears in Collections:Chemistry & Chemical Technology. – 2020. – Vol. 14, No. 1

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