Alkyl Ammonium Tungstate Bonded to Fe3O4@SiO2 Nanoparticles; a highly efficient Catalyst for the Oxidation of Symmetrical Sulfides to Symmetrical Sulfoxides
محورهای موضوعی :
Iranian Journal of Catalysis
Seyed-Mola Khatami
1
,
Mehdi Khalaj
2
,
Majid Ghashang
3
1 - Department of Chemical Industry, Technical and Vocational University (TVU), Tehran, Iran
2 - Department of Chemistry, Islamic Azad University, Buinzahra Branch, Buinzahra, Iran
3 - Department of Chemistry, Najafabad Branch, Islamic Azad University, P.O. Box: 517; Najafabad, Iran
تاریخ دریافت : 1402/05/19
تاریخ پذیرش : 1402/07/26
تاریخ انتشار : 1402/09/10
کلید واژه:
Oxidation,
Magnetic nanocatalysis,
Organic-inorganic hybrids,
Symmetrical sulfide,
Symmetrical sulfoxide,
چکیده مقاله :
A magnetic organic-inorganic hybrid of Fe3O4@SiO2-functionalized propylpiperazine-1,4-diium tungstate (A) nanoparticles with a spherical structure was prepared and completely characterized by XRD, SEM, TGA-DTA, and FT-IR spectral techniques. The magnetic hybrid was used in the oxidation of symmetrical sulfides to symmetrical sulfoxides under ambient conditions. The excellent yields of sulfoxides, easy operation, and recovery, magnetic properties of the catalyst, and environmentally friendly system are the key advantages of this method.
منابع و مأخذ:
Peng, X. Cheng, Y. Chen, J. Yang, Front. Chem. 9 (2021) 714899.
Kumar Singh, V. Tiwari, K. Bihari Mishra, S. Gupta, J. Kandasamy, Beilstein J. Org. Chem. 13 (2017) 1139–1144.
P. Colomer, M.Á. Canales Mayordomo, B. Fernández de Toro, J. Jiménez-Barbero, O. Varela, Eur. J. Org. Chem. 2015 (2015) 1448-1455.
-L. Tong, Z.-F. Fan, J.-W. Yang, Q. Li, Y.-X. Chen, M.-S. Cheng, Y. Liu, Catalysts 9 (2019) 791.
L. Jain, B.S. Rana, B. Singh, A.K. Sinha, A. Bhaumik, M. Nandi, B. Sain, Green Chem. 12 (2010) 374-377.
Carmen Carreno, Chem. Rev. 95 (1995) 1717–1760.
C. Lenstra, V. Vedovato, E.F. Flegeau, J. Maydom, M.C. Willis, Org. Lett. 18 (2016) 2086-2089.
Wang, M. Chen, P. Zhang, W. Li, J. Zhang, J. Am. Chem. Soc. 140 (2018) 3467-3473.
Jia, M. Zhang, S.P. McCollom, A. Bellomo, S. Montel, J. Mao, S.D. Dreher, C.J. Welch, E.L. Regalado, R.T. Williamson, B.C. Manor, N.C. Tomson, P.J. Walsh, J. Am. Chem. Soc. 139 (2017) 8337-8345.
Fu, J. Dong, H. Du, J. Xu, J. Org. Chem. 85 (2020) 2752-2758.
-L. Yue, M. Klussmann, Synlett 27 (2016) 2505-2509.
Signore, S. Samaritani, C. Malanga, R. Menicagli, Synthesis (2006) 762-764.
Battace, T. Zair, H. Doucet, M. Santelli, Synthesis (2006) 3495-3505.
Wang, L. Tang, B. Cai, Z. Yin, Y. Li, L. Xiong, X. Kang, J. Xuan, Y. Pei, M. Zhu, J. Am. Chem. Soc. 144 (2022) 3787-3792.
M. Khodaei, K. Bahrami, A. Karimi, Synthesis (2008) 1682-1684.
Okada, H. Matsumuro, S. Kitagawa, T. Iwai, K. Yamazaki, Y; Kinoshita, Y. Kimura, M. Kirihara, Synlett 26 (2015) 2547-2552.
S. Kim, K. Nehru, S.S. Kim, D.W. Kim, H.C. Jung, Synthesis (2002) 2484-2486.
C.B. Page, B.R. Buckley, C. Elliott, Y. Chan, N. Dreyfus, F. Marken, Synlett 27 (2016) 80-82.
Zhao, H. Zhang, Y. Wang, J. Org. Chem. 81 (2016) 129-134.
Qian, L. Pei, Synlett (2006) 709-712.
H. Ali, D. Kriedelbaugh, T. Wencewicz, Synthesis (2007) 3507-3511.
Xu, L. Yan, S. Wang, P. Wang, A.-X. Yang, X. Li, H. Lua, Z.-Y. Cao, Org. Biomol. Chem. 19 (2021) 8691-8695.
Dehbashi, M. Aliahmad, M.R.M. Shafiee, M. Ghashang, Phosphorus Sulfur Silicon Relat. Elem. 188 (2013) 864-872.
Mary Imelda Jayaseeli, A. Ramdass, S. Rajagopal, Polyhedron 100 (2015) 59-66.
Jafarpour, A. Rezaeifard, M. Ghahramaninezhad, F. Feizpour, Green Chem. 17 (2015) 442-452.
Gogoi, M. Kalita, T. Bhattacharjee, P. Barman, Tetrahedron Lett. 55 (2014) 1028-1030.
-L. Tong, Z.-F. Fan, J.-W. Yang, Q. Li, Y.-X. Chen, M.-S. Cheng, Y. Liu, Catalysts 9 (2019) 791.
Jiang, R.C. Luo, X.T. Zhou, Y.J. Chen, H.B. Jia, Adv. Synth. Catal. 360 (2018) 4402-4411.
Aghavandi, A. Ghorbani-Choghamarani, J. Phys. Chem. Solids 170 (2022) 110952.
Rahimi, M. Azizi, M. Niksefat, M. Heidari, M. Naderi, A. Maleki, Inorg. Chem. Commun. 148 (2023) 110320.
Talukdar, G. Saikia, A. Das, S.Y. Sultana, N.S. Islam, J. Indust. Eng. Chem. 121 (2023) 249-263.
Aliyan, R. Fazaeli, Z. Foroutanfar, D. Richeson, Y. Li, Inorg. Chem. Commun. 149 (2023) 110353.
Khalaj, M. Ghazanfarpour-Darjani, M.R. Talei Bavil Olyai, S.F. Shamami, J. Sul. Chem. 37 (2016) 211.
Varmazyar, S. Sedaghat, A.N. Goli‐Kand, M. Khalaj, S. Arab‐Salmanabadi, J. Het. Chem. 121 (2023) 249-263.
Khalaj, M. Khalaj, J. Chem. Res. 40 (2016) 445.
Khalaj, M. Zarandi, RSC Adv. 12 (2022) 26527.
Khalaj, M. Taherkhani, M. Kalhor, New J. Chem. 45 (2021) 10718.
Khalaj, S.M. Mousavi‐Safavi, N. Farahani, J. Lipkowski, Appl. Organomet. Chem. 34 (2020) e5865.
Khalaj, Arab. J. Chem. 13 (2020) 6403.
Khalaj, M. Taherkhani, L. Payen, A. Klein, Molecules. 28 (2023) 3663.
Khalaj, Polycycl. Aromat. Compd. 43 (2023) 5629.
Maham, M. Khalaj, J. Chem. Res. 38 (2014) 502.
Sajadi, M. Khalaj, S.M. Jamkarani, M. Maham, M. Kashefi, Synth. Commun. 41 (2011) 3053.
Khalaj, M. Ghazanfarpour, RSC Adv. 5 (2015) 80698.
Khalaj, M. Ghazanfarpour-Darjani, F. Barat-Seftejani, A. Nouri, Synlett. 28 (2017) 1445.
Khalaj, M. Taherkhani, F. Naderi, S.M. Mousavi-Safavi, Monatshefte für Chemie-Chem. 149 (2018) 63.
Khalaj, N. Farahani, M. Sadeghpour, H. Rajabzadeh, S.M. Khatami, Synlett, 29 (2018) 894.
Khalaj, Monatshefte für Chemie-Chem. 151 (2020) 945.