journal article·2018-06

CuI@amine-functionalized halloysite as an efficient heterogeneous catalyst for promoting A3 coupling reaction under ultrasonic irradiation: a combination of experimental and DFT simulation

Samaheh Sadjadi, Naeimeh Bahri-Laleh

Journal of Porous Materials· Volume 25· Issue 3
Publisher page

Abstract

Two novel hybrid catalysts based on incorporation of CuI in amine-functionalized halloysite using two different amine functionalization agents, i.e. 3-aminopropyl-triethoxysilane, APTES, and N-[3-(trimethoxysilyl)propyl] ethylenediamine, AEAPTMS, have been synthesized and characterized by using SEM/EDX, XRD, FTIR, ICP, BET, and TGA. Furthermore, the ability of the ligands toward CuI adsorption in the gas and solution phases were compared quantitatively using DFT simulation. The results showed that AEAPTMS-functionalized halloysite has more affinity toward CuI adsorption, which decreases catalyst leaching. This catalyst was successfully used for promoting A3 coupling reaction of aldehydes, phenyl acetylene and amines under ultrasonic irradiation to furnish the corresponding propargylamines in short reaction time and high yields. The synthesized catalyst exhibited high reusability and could be recovered and reused, preserving its catalytic activity.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Catalytic Cross-Coupling Reactions · Chemical Synthesis and Characterization

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

References (53)

Show source-provided references
1. G. Villaverde, A. Corma, M. Iglesias, F. Sanchez, ACS Catal. 2, 399 (2012)10.1021/cs200601w ↗
2. S.V. Katkar, R.V. Jayaram, RSC Adv. 4, 47958 (2014)10.1039/C4RA06275B ↗
3. L.F. Bobadilla, T. Blasco, J.A. Odriozola, Phys. Chem. Chem. Phys. 15, 16927 (2013)10.1039/c3cp52924j ↗
4. M. Hosseini-Sarvari, F. Moeini, New J. Chem. 38, 624 (2014)10.1039/C3NJ01146A ↗
5. B.J. Borah, S.J. Borah, K.l.. Saikia, D.K. Dutta, Catal. Sci. Technol. 4, 4001 (2014)10.1039/C4CY00666F ↗
6. T. Zeng, W.W. Chen, C.M. Cirtiu, A. Moores, G. Song, C.-J. Li, Green Chem. 12, 570 (2010)10.1039/b920000b ↗
7. N. Salam, S.K. Kundu, R. Ali Molla, P. Mondal, A. Bhaumik, S. Manirul Islam, RSC Adv. 4, 47593 (2014)10.1039/C4RA07622B ↗
8. H. Naeimi, M. Moradian, Appl. Organomet. Chem. 27, 300 (2013)10.1002/aoc.2976 ↗
9. H. Zhu, M.L. Du, M.L. Zou, C.S. Xu, Y.Q. Fu, Dalton Trans. 41, 10465 (2012)10.1039/c2dt30998j ↗
10. Y. Zhang, J. Ouyang, H. Yang, Appl. Clay Sci. 95, 252 (2014)10.1016/j.clay.2014.04.019 ↗
11. P. Pasbakhsh, G.J. Churchman, Natural Mineral Nanotubes: Properties and Applications, 1st edn. (Apple Academic Press, Oakville, 2015), pp. 1–49810.1201/b18107 ↗
12. Y. Zhang, H. Yang, Phys. Chem. Miner. 39, 789 (2012)10.1007/s00269-012-0533-9 ↗
13. Y. Zhang, A. Tang, H. Yang, J. Ouyang, Appl. Clay Sci. 119, 8 (2016)10.1016/j.clay.2015.06.034 ↗
14. S. Sadjadi, M. Eskandari, Ultrason. Sonochem. 20, 640 (2013)10.1016/j.ultsonch.2012.09.006 ↗
15. D. Grabka, M. Raczyńska-Żak, K. Czech, P.M. Słomkiewicz, M.A. Jóźwiak, Appl. Clay Sci. 114, 321 (2015)10.1016/j.clay.2015.06.012 ↗
16. R.S. Murali, M. Padaki, T. Matsuura, M.S. Abdullah, A.F. Ismail, Sep. Purif. Technol. 132, 187 (2014)10.1016/j.seppur.2014.05.020 ↗
17. B. Szczepanik, P. Slomkiewicz, Appl. Clay Sci. 124–125, 31 (2016)10.1016/j.clay.2016.01.045 ↗
18. P. Yuan, A. Thill, F. Bergaya, Nanosized Tubular Clay Minerals, 1st edn. (Elsevier, San Diego, 2016), pp. 1–778
19. S. Sadjadi, Organic Nanoreactors: From Molecular to Supramolecular Organic Compounds, 1st edn. (Elsevier, London, 2016), pp. 1–584
20. S. Sadjadi, M.M. Heravi, M. Daraie, Res. Chem. Intermed. 43, 843 (2017)10.1007/s11164-016-2668-7 ↗
21. S. Sadjadi, M.M. Heravi, M. Daraie, Res. Chem. Intermed. 43, 2201 (2017)10.1007/s11164-016-2756-8 ↗
22. S. Sadjadi, M. Eskandari, Monatsh. Chem. 143, 653 (2012)10.1007/s00706-011-0655-7 ↗
23. N. Hadian, S. Hakim, M. Nekoomanesh-Haghighi, N. Bahri-Laleh, Polyolefins J. 1, 33 (2014)
24. S. Sadjadi, M.M. Heravi, M. Daraie, J. Mol. Liq. 231, 98 (2017)10.1016/j.molliq.2017.01.072 ↗
25. S. Sadjadi, Encapsulated Catalyst, 1st edn. (Elsevier, London, 2016), pp. 1–552
26. S. Sadjadi, S. Sadjadi, R. Hekmatshoar, Ultrason. Sonochem. 17, 764 (2010)10.1016/j.ultsonch.2010.01.017 ↗
27. M.J. Frisch, G.W. Trucks, H.B. Schlegel, Gaussian 09. (Gaussian, Inc., Wallingford, 2009)
28. Y. Zhao, D.G. Truhlar, Theor. Chem. Acc. 120, 215 (2008)10.1007/s00214-007-0310-x ↗
29. A. Correa, N. Bahri-Laleh, L. Cavallo, Macromol. Chem. Phys. 214, 1980 (2013)10.1002/macp.201300248 ↗
30. R. Ditchfield, W.J. Hehre, J.A. Pople, J. Chem. Phys. 54, 724 (1971)10.1063/1.1674902 ↗
31. C. Cappelli, A. Rizzo, B. Mennucci, J. Tomasi, R. Cammi, G.L.J.A. Rikken, R. Mathevet, C. Rizzo, J. Chem. Phys. 118, 10712 (2003)10.1063/1.1571813 ↗
32. S. Bordeepong, D. Bhongsuwan, T. Pungrassami, T. Bhongsuwan, Songklanakarin J. Sci. Technol. 33, 599 (2011)
33. L. Zatta, J.E.F. da Costa Gardolinski, F. Wypych, Appl. Clay Sci. 51, 165 (2011)10.1016/j.clay.2010.10.020 ↗
34. P. Yuan, P.D. Southon, Z. Liu, M.E.R. Green, J.M. Hook, S.J. Antill, C.J. Kepert, J. Phys. Chem. C 112, 15742 (2008)10.1021/jp805657t ↗
35. H. Naeimi, R. Shaabani, Ultrason. Sonochem. 34, 246 (2017)10.1016/j.ultsonch.2016.05.043 ↗
36. A. Elhampour, M. Malmir, E. Kowsari, F. Boorboorajdari, F. Nemati, RSC Adv. 6, 96623 (2016)10.1039/C6RA18810A ↗
37. L. Shi, Y.Q. Tu, M. Wang, F.M. Zhang, C.A. Fan, Org. Lett. 6, 1001 (2004)10.1021/ol049936t ↗
38. M.M. Heravi, S. Sadjadi, S. Sadjadi, H.A. Oskooie, F.F. Bamoharram, Ultrason. Sonochem. 16, 708 (2009)10.1016/j.ultsonch.2009.02.010 ↗
39. M.M. Heravi, S. Sadjadi, S. Sadjadi, H.A. Oskooie, F.F. Bamoharram, Ultrason. Sonochem. 16, 718 (2009)10.1016/j.ultsonch.2009.04.004 ↗
40. N.P. Eagalapati, A. Rajack, Y.L.N. Murthy, J. Mol. Catal. A 381, 126 (2014)10.1016/j.molcata.2013.10.009 ↗
41. B. Jyoti Borah, S. Jyoti Borah, K. Saikia, D. Kumar, Dutta, Catal. Sci. Technol. 44, 4001 (2014)10.1039/C4CY00666F ↗
42. F. Movahedia, H. Masrouria, M.Z. Kassaee, J. Mol. Catal. A 395, 52 (2014)10.1016/j.molcata.2014.08.007 ↗
43. K.V.V. Satyanarayana, P. Atchuta Ramaiah, Y.L.N. Murty, M.R. Chandra, S.V.N. Pammi, Catal. Commun. 25, 50 (2012)10.1016/j.catcom.2012.03.031 ↗
44. B. Karimi, M. Gholinejad, M. Khorasani, Chem. Commun. 48, 8961 (2012)10.1039/c2cc33320a ↗
45. X. Xiong, H. Chen, R. Zhu, Catal. Commun. 54, 94 (2014)10.1016/j.catcom.2014.05.030 ↗
46. M.J. Albaladejo, F. Alonso, Y. Moglie, M. Yus, Eur. J. Org. Chem. 2012, 3093 (2012)10.1002/ejoc.201200090 ↗
47. M.S. Hosseini, F. Moeini, New J. Chem. 38, 624 (2014)10.1039/C3NJ01146A ↗
48. F. Nador, M.A. Volpe, F. Alonso, A. Feldhoff, A. Kirschning, G. Radivoy, Appl. Catal. A 455, 39 (2013)10.1016/j.apcata.2013.01.023 ↗
49. M. Kidwai, A. Jahan, J. Iran. Chem. Soc. 8, 462 (2011)10.1007/BF03249079 ↗
50. N. Bahri-Laleh, Appl. Surf. Sci. 379, 395 (2016)10.1016/j.apsusc.2016.04.034 ↗
51. R. Bazvand, N. Bahri-Laleh, M. Nekoomanesh-Haghighi, H. Abedini, Des. Monomers Polym. 18, 599 (2015)10.1080/15685551.2015.1041089 ↗
52. N. Bahri-Laleh, A. Poater, L. Cavallo, S.A. Mirmohammadi, Dalton Trans. 43, 15143 (2014)10.1039/C4DT01617C ↗
53. N. Bahri-Laleh, L. Falivene, L. Cavallo, Polyolefins J. 1, 139 (2014)