journal article·2019-02

SBA-15@adenine–Pd: a novel and green heterogeneous nanocatalyst in Suzuki and Stille reactions and synthesis of sulfides

Taiebeh Tamoradi, Mohammad Ghadermazi, Arash Ghorbani-Choghamarani

Journal of Porous Materials· Volume 26· Issue 1
Publisher page

Abstract

In the present study, anchored palladium onto the surface of organically modified mesoporous silica was successfully prepared via simple and inexpensive procedure. The prepared nanocatalyst was considered as robust and clean nano-reactor catalyst for Suzuki and Stille reactions and synthesis of sulfide. This ecofriendly heterogeneous catalyst was characterized by Fourier transform infrared spectroscopy, transmission and scanning electron microscopies, energy-dispersive X-ray spectroscopy, inductively coupled plasma optical emission spectroscopy, X-ray diffraction, thermal gravimetric analysis, and N2 adsorption and desorption. Use of green medium, easy separation and workup, excellent reusability of the nanocatalyst, and short reaction time are outstanding advantages of this method.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Sulfur-Based Synthesis Techniques · Catalytic Cross-Coupling Reactions · Chemical Synthesis and Reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (48)

Show source-provided references
1. M. Nikoorazm, A. Ghorbani-Choghamarani, N. Noori, B. Tahmasbi, Appl. Organometal. Chem. 30, 843–851 (2016)10.1002/aoc.3512 ↗
2. L. Yin, J. Liebscher, Chem. Rev. 107, 133–173 (2007)10.1021/cr0505674 ↗
3. T. Tamoradi, A. Ghorbani-Choghamarani, M. Ghadermazi, New J. Chem. (2017). https://doi.org/10.1039/C7NJ02337E10.1039/C7NJ02337E ↗
4. M.R. Maurya, A.K. Chandrakar, S. Chand, J. Mol. Catal. A 263, 227–237 (2007)10.1016/j.molcata.2006.08.084 ↗
5. M. Darabi, T. Tamoradi, M. Ghadermazi, A. Ghorbani-Choghamarani, Trans. Metal Chem. (2017). https://doi.org/10.1007/s11243-017-0177-110.1007/s11243-017-0177-1 ↗
6. A. Orejon, A.M. Masdeu-Bulto, P. Salagre, S. Castillon, C. Claver, A. Padilla, B. Almena, F. Luis Serrano, Ind. Eng. Chem. Res. 47, 8032–8036 (2008)10.1021/ie8002599 ↗
7. Y.S. Fu, S.J. Yu, Angew. Chem. Int. Ed. 40, 437–440 (2001)10.1002/1521-3773(20010119)40:2<437::AID-ANIE437>3.0.CO;2-N ↗
8. P. McMorn, G.J. Hutchings, Chem. Soc. Rev. 33, 108–122 (2004)10.1039/b200387m ↗
9. N. Noori, M. Nikoorazm, A. Ghorbani-Choghamarani, Catal. Lett. (2017). https://doi.org/10.1007/s10562-016-1905-410.1007/s10562-016-1905-4 ↗
10. B. Xue, P. Chen, Q. Hong, J. Lin, K.L. Tan, J. Mater. Chem. 11, 2378–2381 (2001)10.1039/b100618p ↗
11. A. Ghorbani-Choghamarani, Z. Taherinia, RSC Adv. 6, 59410–59421 (2016)10.1039/C6RA02264B ↗
12. M.A. Zolfigol, V. Khakyzadeh, A.R. Moosavi-Zare, A. Rostami, A. Zare, N. Iranpoor, M.H. Beyzavi, R. Luque, Green Chem. 15, 2132–2140 (2013)10.1039/c3gc40421h ↗
13. B. Tahmasbi, A. Ghorbani‑Choghamarani, Catal. Lett. (2017). https://doi.org/10.1007/s10562-016-1927-y10.1007/s10562-016-1927-y ↗
14. S. Ghosh, R. Dey, S. Ahammed, B.C. Ranu, Clean. Technol. Environ. Policy 16, 1767–1771 (2014)10.1007/s10098-013-0658-7 ↗
15. B. Karimi, A. Zamani, Org. Biomol. Chem. 10, 4531–4536 (2012)10.1039/c2ob07176b ↗
16. A. Ghorbani-Choghamarani, F. Nikpour, F. Ghorbani, F. Havasi, RSC Adv. 5, 33212–33220 (2015)10.1039/C5RA01934F ↗
17. J. Panpranota, K. Pattamakomsana, J.G. Goodwin Jr., P. Praserthdama, Catal. Commun. 5, 583–590 (2004)10.1016/j.catcom.2004.07.008 ↗
18. N. Noori, M. Nikoorazm, A. Ghorbani-Choghamarani, Micro. Meso. Mater. 234, 166–175 (2016)10.1016/j.micromeso.2016.06.036 ↗
19. N. Marín-Astorgaa, G. Pecchia, J.L.G. Fierrob, P. Reyesa, J. Mol. Catal. A 231, 67–74 (2005)10.1016/j.molcata.2005.01.004 ↗
20. F. Havasi, A. Ghorbani-Choghamarani, F. Nikpour, Micro. Meso. Mater. 224, 26–35 (2016)10.1016/j.micromeso.2015.10.036 ↗
21. M. Khanmoradi, M. Nikoorazm, A. Ghorbani‑Choghamarani, Catal. Lett. (2017). https://doi.org/10.1007/s10562-016-1957-510.1007/s10562-016-1957-5 ↗
22. T. Itoh, T. Mase, Org. Lett. 6, 4587–4590 (2004)10.1021/ol047996t ↗
23. K. Swapna. S.N. Murthy, M.T. Jyothi, Y.V.D. Nageswar, Org. Biomol. Chem. 9, 5989–5996 (2011)10.1039/c1ob05597f ↗
24. T. Kondo, T. Mitsudo, Chem. Rev. 100, 3205–3220 (2000)10.1021/cr9902749 ↗
25. L. Rout, P. Saha, S. Jammi, T. Punniyamurthy, Eur. J. Org. Chem. 19, 640–643 (2008)10.1002/ejoc.200700978 ↗
26. D. Dreisinger, Hydrometallurgy 83, 1–4 (2006)10.1016/j.hydromet.2006.03.032 ↗
27. W. Roediger, W. Babidge, Mol. Cell. Biochem. 206, 159–167 (2000)10.1023/A:1007034417320 ↗
28. J. Davarpanah, A.R. Kiasat, Catal. Commun. 46, 75–80 (2014)10.1016/j.catcom.2013.11.022 ↗
29. G.M. Dhar, G.M. Kumaran, M. Kumar, K.S. Rawat, L.D. Sharma, B.D. Raju, K.S.R. Rao, Catal. Today 99, 309–314 (2005)10.1016/j.cattod.2004.10.005 ↗
30. G. Muthu Kumaran, S. Garg, K. Soni, M. Kumar, L.D. Sharma, G. Murali Dhar, K.S. Rama Rao, Appl. Catal. A 305, 123–129 (2006)10.1016/j.apcata.2006.02.057 ↗
31. Y.Y. Peng, J. Liu, X. Lei, Z. Yin, Green Chem. 12, 1072–1075 (2010)10.1039/c000739k ↗
32. L. Bai, J.X. Wang, Adv. Synth. Catal. 350, 315–320 (2007)10.1002/adsc.200700361 ↗
33. A. Ghorbani-Choghamarani, B. Tahmasbi, P. Moradi, Appl. Organometal. Chem. 30, 422–430 (2016)10.1002/aoc.3449 ↗
34. A. Ghorbani‑Choghamarani, B. Tahmasbi, N. Noori, R. ·Ghafouri‑nejad, J. Iran Chem. Soc. (2017). https://doi.org/10.1007/s13738-016-1020-x10.1007/s13738-016-1020-x ↗
35. P. Zhao, H. Yin, H. Gao, C. Xi., J. Org. Chem. 78, 5001–5006 (2013)10.1021/jo400709s ↗
36. L. Baia,.J.X. Wanga, Adv. Synth. Catal. 350, 315–320 (2007)10.1002/adsc.200700361 ↗
37. Y. Zhou, J. Chem. Res. 40, 305–307 (2016)10.3184/174751916X14605556925623 ↗
38. B.H. Mackl, R.G. Mayrick, Trans. Faraday Soc. 58, 238–243 (1962)10.1039/TF9625800238 ↗
39. G. Azadi, Z. Taherinia, A. Naghipour, A. Ghorbani-Choghamarani, J. Sulfur Chem. (2017). https://doi.org/10.1080/17415993.2017.128726510.1080/17415993.2017.1287265 ↗
40. A. Modak, J. Mondal, M. Sasidharan, A. Bhaumik, Green Chem. 13, 131317–131331 (2011)10.1039/c1gc15045f ↗
41. T. Chen, J. Gao, M. Shi, Tetrahedron 62, 6289–6294 (2006)10.1016/j.tet.2006.04.034 ↗
42. Q. Xu, W.L. Duan, Z.Y. Lei, Z.B. Zhu, M. Shi, Tetrahedron 61, 11225–11229 (2005)10.1016/j.tet.2005.09.010 ↗
43. S. Singha, M. Sahoo, K.M. Parida, Dalton Trans. 40, 7130–7136 (2011)10.1039/c1dt10697j ↗
44. H.A. Patel, A.L. Patel, A.V. Bedekar, Appl. Organometal. Chem. 29, 1–6 (2015)10.1002/aoc.3234 ↗
45. M. Nasrollahzadeh, A. Azarian, M. Maham, A. Ehsani, J. Ind. Eng. Chem. 21, 746–748 (2015)10.1016/j.jiec.2014.04.006 ↗
46. V.W. Faria, D.G.M. Oliveira, M.H.S. Kurz, F.F. Goncalves, C.W. Scheeren, G.R. Rosa, RSC Adv. 4, 13446–13452 (2014)10.1039/C4RA01104J ↗
47. M. Nasrollahzadeh, S.M. Sajadi, M. Maham, J. Mol. Catal. A 396, 297–303 (2015)10.1016/j.molcata.2014.10.019 ↗
48. S.J. Sabounchei, A. Hashemi, Inorg. Chem. Commun. 47, 123–127 (2014)10.1016/j.inoche.2014.07.027 ↗