catalytic applications of coated nanopalladium particles coated on modified GO by Thymbraspicata extract in Suzuki coupling reactions | ||
| شیمى کاربردى روز | ||
| Volume 16, Issue 58, April 2021, Pages 233-244 PDF (1.26 M) | ||
| Document Type: Original Article | ||
| DOI: 10.22075/chem.2021.19567.1784 | ||
| Authors | ||
| Malak Hekmati* 1; Mohammad Yousefi2; Hakimeh Ziyadi1; Ensieh Ghasemi1; parisa Safari Mehr3; hojat Veisi3; Behrooz Maleki4 | ||
| 1Department of Chemistry, School of Medicinal Chemistry, Tehran University of Medical Sciences, Tehran, Iran | ||
| 2Department of Chemistry, Imam Khomeini Memorial Unit, Rey, Islamic Azad University, Tehran, Iran | ||
| 3Department of Chemistry, Faculty of Basic Sciences, Payame Noor University, Tehran, Iran | ||
| 4Hakim Sabzevari University, Sabzevar | ||
| Receive Date: 14 January 2020, Revise Date: 01 July 2020, Accept Date: 05 January 2021 | ||
| Abstract | ||
| In this research coated palladium nanoparticles was synthesized on modified GO by thymbraspicata extract with simple and green procedure and used as adequate and renewable nanocatalyst for Suzuki coupling reactions between phenylboronic acid and different aryl halides. The Pd NPs/RGO Nanocatalyst was synthesized by surface modification of GO and in-Situ reduction. The extract of Thymbraspicata was used as a reducing and immobilizing agent for Pd nanoparticles. The results show that Pd(0) nanoparticles are completely dispersed on the GO functionalized surface. Pd NPs/RGO nanocatalyst as a recoverable nanocatalyst shows high catalytic activity in Suzuki coupling reaction. In addition, the synthesized catalyst can be reused several times without significant altering its catalytic activity. | ||
| Keywords | ||
| Green synthesis; Graphene; Pd Nanoparticle; Suzuki | ||
| References | ||
|
[1] A. Balanta, C. Godard, C. Claver, Chem. Soc. Rev. 40 (2011) 4973.
[2] S. Kotha, K. Lahiri, D. Kashinath, Tetrahedron. 58 (2002) 9633.
[3] R.K. Borah, A. Mahanta, A. Dutta, U. Bora, A.J. Thakur,Appl. Organomet. Chem. 31 (2017) e3784.
[4] R. Jana, T.P. Pathak, M.S. Sigman, Chem. Rev. 111 (2011) 1417.
[5] P. Gautam, M. Dhiman, V. Polshettiwar, B.M. Bhanage, Green Chem. 18 (2016) 5890.
[6] a) H. Veisi, M. Ghorbani, S. Hemmati, Mat. Sci. Eng. C 98 (2019) 584 ; b) H. Veisi, P. Safarimehr, S. Hemmati, Mat. Sci. Eng. C 96 (2019) 310.
[7] MR. Yadav, M. Nagaoka, M. Kashihara, RL. Zhong, T. Miyazaki, S. Sakaki, Y. Nakao, J. Am. Chem. Soc. 139 (2017) 9423.
[8] (a) M. Cametti, Z. Dzolic, Chem. Commun. 50 (2014) 8273–8286; (b) M. Liu, R. Zhang, W. Chen, Chem. Rev., 114(2014) 10, 5117; (c) C. Zhang, R. Zhang, S. He, L. Li, X. Wang, M. Liu, W. Chen, ChemCatChem, 96 (2017) 980.
[10] P. Avouris, Graphene: electronic and photonic properties and devices, Nano Lett. 10 (2010) 4285.
[11] C. Noguez, I.L. Garzon, Chem. Soc. Rev. 38 (2009) 757.
[12] J.D. Roy-Mayhew, I.A. Aksay, Chem. Rev. 114 (2014) 6323.
[13] J. Liu, M. Durstock, L. Dai, Energy Environ. Sci. 7 (2014) 1297.
[14] F. Yavari, N. Koratkar, J. Phys. Chem. Lett. 3 (2012) 1746.
[15] (a) L. Rashidzadeh, A. Noorbakhsh, J. Of Applied Chemistry, 48 (1397) 310, in Persian ; (b) Z. Wang, C. Xu, X.Li, Z. Liu,Colloids and Surfaces A: Physicochem. Eng. Aspects 485 (2015) 102.
[16] M. Hamzelooian, K. Ghasemi, F. Soleimanian, J. Of Applied Chemistry, 52 (1398) 103, in Persian.
[17] a) Z. Wang, C. Xu, M. Zhao, C. Zhao, RSC Adv. 4 (2014) 47021. ; b)Hemmati S, Mehrazin L, Ghorban H, Garakani SH, Mobaraki TH, Mohammadi P, Veisi H. RSC Adv., 8 (2018) 21020.
[18] S. Shi, F. Chen, E.B. Ehlerding, W. Cai, Bioconjug. Chem. 19 (2014)2033.
[19] J. Ando, T. Yano, K. Fujita, S. Kawata, Phys. Chem. Chem. Phys. 15 (2013) 13713.
[20] P.V. Kamat, J. Phys. Chem.Lett. 1 (2010) 520.
[21] S.I. El-Hout, S.M. El-Sheikh, H.M.A. Hassan, F.A. Harraz, I.A. Ibrahim, E.A. El-Sharkawy, Appl. Catal., A: Gen. . 503 (2015) 176.
[22]H. Veisi, T. Tamoradi, B. Karmakar, P. Mohammadi, S. Hemmati, Mat. Sci. Eng. C, 104 (2019) 109919.
[23] (a) M. Shahriary, H. Veisi, M. Hekmati, S. Hemmati, Mat. Sci. Eng. C. 90 (2018) 57; (b)S Abbasi, M Hekmati, Applied Organometallic Chemistry 2017, 31 (5) e3600
[24] F. R. Fortea, Pérez, I. Schlegel, M. Julve, D. Armentano, G. De Munno, S. E. Stiriba, J.Organomet.Chem. . 743 (2013) 102.
[25] Q. X. Liu, W. Zhang, X. J. Zhao, Z. X. Zhao, M. C. Shi, X. G. Wang, Eur. J. Org.
Chem. . (2013) 1253 .
[26] M. Ghiaci, M. Zargani, F. Moeinpour, A. khojastehnezhad, Appl. Organometal.Chem. . 28 (2014) 589.
[27] V. I. de Paula, C. A. Sato, R. Buffon, J. Braz. Chem. Soc. . 23 (2012) 258.
[28] S. M. ShakilHussain, M. B. Ibrahim, A. Fazal, R. Suleiman, M. Fettouhi, B. El Ali, Polyhedron, 70 (2014) 39.
[29] S. Sobhani, M. S. Ghasemzadeh, M. Honarmand, F. Zarifi, RSC Adv. . 4 (2014) 44166.
[30] S. Sobhani, F. Zarifi, Chinese J. Catal. (2015) 555. | ||
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