Supramolecular grafting and stabilization of manganese complex on kryptofix23 modified Fe3O4@carbon nanosphere: as highly efficient, reusable, and clean nanocatalyst for xanthene’s unusual coupling
Source abstract
Abstract
Abstract Grafting and stabilization of metal complexes for increasing catalytic activity have remained an enormous challenge in the catalytic arena. However, designing a catalytic system with complementary properties including high surface area, high loading, and easy separation offers a promising route for efficient utilization of magnetic material for various applications. Herein, novel core-shell nanosphere catalyst (Fe3O4@C/KP23@MnCl2) was successfully synthesized with a magnetite core encapsulated in a carbon shell. It was modified using CPTES (3-chloropropyltriethoxysilane) and Kryptofix23 (KP23) ligand in the carbon surface for conversion to Fe3O4@C/KP23 support. The Manganese complex was coordinated onto the KP23 ligand decorated Fe3O4@C to improve the unusual coupling xanthenes in ethanol. It was found proposed nanocatalyst is greener, recyclable, and more suitable option for the large-scale application and provide some new insights into organic transformation.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Multicomponent Synthesis of Heterocycles · Catalytic Cross-Coupling Reactions · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (55)
Show source-provided references
1. Y. Wang, S. Furukawa, X. Fu, N. Yan, ACS Catal. 10, 311 (2019)10.1021/acscatal.9b03744 ↗
2. R.D. Andrei, E. Borodina, D. Minoux, N. Nesterenko, J.P. Dath, C. Cammarano, V. Hulea, Ind. Eng. Chem. Res. 59, 1746 (2020)10.1021/acs.iecr.9b05576 ↗
3. T.K. Todorova, M.W. Schreiber, M. Fontecave, ACS Catal. 10, 1754 (2019)10.1021/acscatal.9b04746 ↗
4. B. Delmon, J. Therm. Anal. Calorim. 90, 49 (2007)10.1007/s10973-007-8476-y ↗
5. S. Liu, F. Lu, R. Xing, J.J. Zhu, Eur. J. Chem. 17, 620 (2017)10.1002/chem.201001789 ↗
6. D.E. Elliott, W.X. Zhang, Chem. Eur. 35, 4922 (2011)
7. H.P. Cong, J.J. He, Y. Lu, S.H. Yu, Small 6, 169 (2010)10.1002/smll.200901360 ↗
8. X. Yang, X. Zhang, Y. Ma, Y. Huang, Y. Wang, Y. Chen, J. Mater. Chem. 19, 2710 (2019)10.1039/b821416f ↗
9. Y.G. Adewuyi, Environ. Sci. Technol. 39, 8557 (2005)10.1021/es0509127 ↗
10. L. Luo, Y. Wang, M. Zhu, X. Cheng, X. Zhang, X. Meng, X. Huang, H. Hao, Ind. Eng. Chem. Res. 58, 699 (2019)
11. Y. Fu, X. Wang, Ind. Eng. Chem. Res. 50, 7210 (2011)10.1021/ie200162a ↗
12. S.C. Tsang, V. Caps, I. Paraskevas, D. Chadwick, D. Thompsett, Angew. Chem. Int. Ed. 116, 5763 (2004)10.1002/ange.200460552 ↗
13. Q. Zhang, X. Yang, J. Guan, A.C.S. Appl, Nano Mater. 2, 4681 (2019)
14. W. Wu, Q. He, C. Jiang, Nanoscale Res. Lett. 3, 397 (2008)10.1007/s11671-008-9174-9 ↗
15. K. Aguilar-Arteaga, J.A. Rodriguez, E. Barrado, Anal. Chim. Acta 674, 157 (2010)10.1016/j.aca.2010.06.043 ↗
16. M. Liong, J. Lu, M. Kovochich, T. Xia, S.G. Ruehm, A.E. Nel, F. Tamanoi, J.I. Zink, ACS Nano 2, 889 (2008)10.1021/nn800072t ↗
17. T.J. Yoon, K.N. Yu, E. Kim, J.S. Kim, B.G. Kim, S.H. Yun, B.H. Sohn, M.H. Cho, J.K. Lee, S.B. Park, Small 2, 209 (2006)10.1002/smll.200500360 ↗
18. G.M. Lanza, P.M. Winter, S.D. Caruthers, A.M. Morawski, A.H. Schmieder, K.C. Crowder, S.A. Wickline, J. Nucl. Cardiol. 11, 733 (2004)10.1016/j.nuclcard.2004.09.002 ↗
19. D.B. Shieh, F.Y. Cheng, C.H. Su, C.S. Yeh, M.T. Wu, Y.N. Wu, C.Y. Tsai, C.L. Wu, D.H. Chen, C.H. Chou, Biomaterials 26, 7183 (2005)10.1016/j.biomaterials.2005.05.020 ↗
20. H. Gu, P.L. Ho, K.W. Tsang, L. Wang, B. Xu, J. Am. Chem. Soc. 125, 15702 (2003)10.1021/ja0359310 ↗
21. Y.C. Chang, D.H. Chen, J. Coll. Interf. Sci. 283, 446 (2005)10.1016/j.jcis.2004.09.010 ↗
22. J.F. Liu, Z.S. Zhao, G.B. Jiang, Environ. Sci. Technol. 42, 6949 (2008)10.1021/es800924c ↗
23. S.S. Banerjee, D.H. Chen, J. Hazard. Mater. 147, 792 (2007)10.1016/j.jhazmat.2007.01.079 ↗
24. N. Noroozi Pesyan, V. Golsanamloo, S. Ganbari, E. Şahin, Tetrahedron Lett. 53, 4096 (2012)10.1016/j.tetlet.2012.05.116 ↗
25. N. Kaur, P. Dhairwal, A. Brar, G. Kaur, A. Bhalla, C. Prakash, G.R. Chaudhary, Mater. Today Chem. 14, 100194 (2019)10.1016/j.mtchem.2019.100194 ↗
26. E. Doustkhah, M. Heidarizadeh, S. Rostamnia, A. Hassankhani, B. Kazemi, X. Liu, Mater. Lett. 216, 139 (2018)10.1016/j.matlet.2018.01.014 ↗
27. J. Pan, X. Li, X. Qiu, X. Luo, N. Jiao, Org. Lett. 20, 2762 (2018)10.1021/acs.orglett.8b00992 ↗
28. M. Nikpassand, L.Z. Fekri, S. Sahrapeima, S. Shariati, Lett. Org. Chem. 13, 578 (2016)10.2174/1570178613666160927111534 ↗
29. R.M. Ion, A. Planner, K. Wiktorowicz, D. Frackowiak, Acta Biochim. Pol. 45, 833 (1998)10.18388/abp.1998_4279 ↗
30. M. Ahmad, T.A. King, D.K. Ko, B.H. Cha, J. Lee, J. Phys. 35, 1473 (2002)
31. J.S. Martins, A.A. Bartolomeu, W.H. Dos Santos, L.C. da Silva Filho, E.F. De Oliveira, F.C. Lavarda, A. Cuin, C. Legnani, I.O. Maciel, B. Fragneaud, W.G. Quirino, J. Phys. Chem. 121, 12999 (2017)
32. P. Poupelin, G. Saint-Ruf, O. Foussard-Blanpin, G. Narcisse, G. Uchida-Ernouf, R. Lacroix, Chem. Inf. Dienst. 9, 50 (1978). https://doi.org/10.1002/chin.19782515410.1002/chin.197825154 ↗
33. R.C. Hunter, T.J. Beveridge, Appl. Environ. Microbiol. 71, 2501 (2005)10.1128/AEM.71.5.2501-2510.2005 ↗
34. N.K.S. Mogha, K. Chaudhary, G. Kumar, D.T. Masram, ACS Omega 3, 16377 (2018)10.1021/acsomega.8b01781 ↗
35. Y. Xia, H. Yang, C.T. Campbell, Acc. Chem. Res. 46, 1671 (2013)10.1021/ar400148q ↗
36. M. Nikoorazm, B. Tahmasbi, S. Gholami, P. Moradi, Appl. Organometal. Chem. 34, e5919 (2020)10.1002/aoc.5919 ↗
37. M. Nikoorazm, Z. Rezaei, B. Tahmasbi, J. Porous Mater. 27, 671 (2020)10.1007/s10934-019-00835-6 ↗
38. M. Nikoorazm, P. Moradi, N. Noori, J. Porous Mater. 27, 1159 (2020)10.1007/s10934-020-00894-0 ↗
39. M. Nikoorazm, P. Moradi, N. Noori, G. Azadi, J. Iran. Chem. Soc. 18, 467 (2021)10.1007/s13738-020-02040-8 ↗
40. B. Tahmasbi, A. Ghorbani-Choghamarani, New J. Chem. 43, 14485 (2019)10.1039/C9NJ02727K ↗
41. B. Tahmasbi, A. Ghorbani-Choghamarani, P. Moradi, New J. Chem. 44, 3717 (2020)10.1039/C9NJ06129K ↗
42. P. Moradi, M. Hajjami, RSC Adv. 11, 25867 (2021)10.1039/D1RA03578A ↗
43. M. Nikoorazm, N. Noori, B. Tahmasbi, S. Faryadi, Transit. Met. Chem. 42, 469 (2017)10.1007/s11243-017-0151-y ↗
44. M.O. Sydnes, Curr. Org. Chem. 18, 312 (2014)10.2174/13852728113176660145 ↗
45. R. Mohammadi, E. Eidi, M. Ghavami, M.Z. Kassaee, J. Mol. Catal. A Chem. 393, 309 (2014)10.1016/j.molcata.2014.06.005 ↗
46. H. Kefayati, S.J. Bazargard, P. Vejdansefat, S. Shariati, A.M. Kohankar, Dyes Pigm. 125, 309 (2016)10.1016/j.dyepig.2015.10.034 ↗
47. F. Rajabi, M. Pinilla-de Dios, M. Abdollahi, R. Luque, Catal. Commun. 120, 95 (2019)10.1016/j.catcom.2018.10.004 ↗
48. M. Kidwai, V. Bansal, A. Kumar, S. Mozumdar, Green Chem. 9, 742 (2007)10.1039/b702287e ↗
49. J. Liu, Z. Sun, Y. Deng, Y. Zou, C. Li, X. Guo, L. Xiong, Y. Gao, F. Li, D. Zhao, Angew. Chem. Int. Ed. 48, 5875 (2009)10.1002/anie.200901566 ↗
50. P. Russo, D. Acierno, M. Palomba, G. Carotenuto, R. Rosa, A. Rizzuti, C. Leonelli, J. Nanotechnol. 2012, 1–8 (2012)10.1155/2012/728326 ↗
51. D.J. Lockwood, JOSA 63, 374 (1973)10.1364/JOSA.63.000374 ↗
52. A. Tawansi, A. El-Khodary, H.M. Zidan, S.I. Badr, Polym. Test. 21, 381 (2002)10.1016/S0142-9418(01)00100-3 ↗
53. N.K. Subodh, K. Mogha, G. Chaudhary, D.T. Kumar, ACS Omega 3, 16377 (2018)10.1021/acsomega.8b01781 ↗
54. L. Moradi, M. Mirzaei, RSC Adv. 9, 19940 (2019)10.1039/C9RA03312B ↗
55. B. Karami, S.J. Hoseini, K. Eskandari, A. Ghasemi, H. Nasrabadi, Catal. Sci. Technol. 2, 331 (2012)10.1039/C1CY00289A ↗