Skip to main content
Log in

Synthetic and catalytic perspectives of polystyrene supported metal catalyst

  • Published:
Journal of the Iranian Chemical Society Aims and scope Submit manuscript

Abstract

The field of organic synthesis is evolving, demanding cleaner, more efficient and selective processes. With a focus on environmental cleanliness, recent years have witnessed remarkable progress in synthesizing and designing molecules, moving away from indiscriminate and wasteful practices. A notable approach involves the use of insoluble polymers and solid-supported agents. By employing suitably functionalized polymer supports, the concept of selectively capturing, filtering, and releasing the desired product in a pure form has emerged as a crucial need. While solid-supported reagents have a history in organic synthesis, recent advancements have introduced numerous improved reagents, many of which are commercially available. The appeal of solid-supported reagents lies in their ability to drive reactions to completion by using excess reagents. Simple filtration for product removal ensures clean chemistry, with the added benefit of isolating the solid-supported species. This isolation proves crucial in cases where the reagent acts as a catalyst or when spent materials can be regenerated and recycled. The attractiveness of this approach extends to immobilizing toxic reagents, enhancing their safety and acceptability by preventing their release into solution. Multiple reagents can be used simultaneously, and site isolation allows incompatible species to coexist, enabling unique one-pot transformations. Thus, a search for sustainable catalytic methods has intensified in recent times as a result of a need for environmentally friendly systems with high activity, efficiency, and selectivity. Heterogeneous catalysts have emerged as a significant field in the synthesis of crucial molecules, due to their improved thermal stability, selectivity, and recyclability. However, drawbacks such as metal leaching and reduced enantioselectivity for asymmetric synthesis persist. This review aims to shed light on the preparation of polymer-supported ligands and their heterogeneous catalytic system by exploring the synthetic methods used to attach ligands and metal complexes to polymer supports. The review emphasizes the diverse range of applications for the supported complexes, providing a comprehensive analysis of their scope and impact.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 45
Scheme 46
Scheme 47
Scheme 48
Scheme 49
Scheme 50
Scheme 51
Scheme 52
Scheme 53
Scheme 54
Scheme 55
Scheme 56
Scheme 57
Scheme 58
Scheme 59
Scheme 60
Scheme 61
Scheme 62
Scheme 63
Scheme 64
Scheme 65
Scheme 66
Scheme 67
Scheme 68
Scheme 69
Scheme 70
Scheme 71
Scheme 72
Scheme 73
Scheme 74
Scheme 75
Scheme 76
Scheme 77
Scheme 78
Scheme 79
Scheme 80
Scheme 81
Scheme 82
Scheme 83
Scheme 84
Scheme 85
Scheme 86
Scheme 87
Scheme 88
Scheme 89
Scheme 90
Scheme 91
Scheme 92
Scheme 93
Scheme 94
Scheme 95
Scheme 96
Scheme 97
Scheme 98
Scheme 99
Scheme 100
Scheme 101
Scheme 102
Scheme 103
Scheme 104
Scheme 105
Scheme 106
Scheme 107
Scheme 108
Scheme 109
Scheme 110
Scheme 111
Scheme 112
Scheme 113
Scheme 114
Scheme 115

Similar content being viewed by others

References

  1. J. Hagen, Industrial catalysis: a practical approach, 2nd edn. (Wiley-VCH Verlag, Weinheim, Germany, 2006)

    Google Scholar 

  2. N.C. Fletcher, Chiral 2,20 -bipyridines: Ligands for asymmetric induction. J. Chem. Soc. Perkin Trans. 1, 1831–1842 (2002)

    Article  Google Scholar 

  3. Y. Cao, C. Liang, L. Shen, Z. Zhang, T. Jiang, D. Li, W. Zou, J. Wang, K. Zong, D. Liang, D. Ji, Y. Cao, Front. Endocrinol. 13, 906849 (2022). https://doi.org/10.3389/fendo.2022.906849

    Article  Google Scholar 

  4. Y. Gou, G. Huang, J. Li, F. Yang, H. Liang, Coord. Chem. Rev. 441, 213975 (2021). https://doi.org/10.1016/j.ccr.2021.213975

    Article  CAS  Google Scholar 

  5. J. Li, T. Chen, Coord. Chem. Rev. 418, 213355 (2020). https://doi.org/10.1016/j.ccr.2020.213355

    Article  CAS  Google Scholar 

  6. J. Zhang, L. Xu, W.-Y. Wong, Coord. Chem. Rev. 355, 180–198 (2018). https://doi.org/10.1016/j.ccr.2017.08.007

    Article  CAS  Google Scholar 

  7. W. Zhuo, H. Xu, R. Huang, J. Zhou, Z. Tong, H. Xie, X. Zhang, J. Iran. Chem. Soc. 14, 2557–2566 (2017). https://doi.org/10.1007/s13738-017-1190-1

    Article  CAS  Google Scholar 

  8. K.R. Gruenwald, A.M. Kirillov, M. Haukka, J. Sanchiz, A.J.L. Pombeiro, Dalton Trans. 12, 2109 (2009) https://doi.org/10.1039/b813160k

  9. P. Saisaha, J.W. de Boer, W.R. Browne, Chem. Soc. Rev. 42(5), 2059–2074 (2013). https://doi.org/10.1039/c2cs35443h

    Article  CAS  PubMed  Google Scholar 

  10. S. Hübner, J.G. de Vries, V. Farina, Adv. Synth. Catal. 358(1), 3–25 (2015). https://doi.org/10.1002/adsc.201500846

    Article  CAS  Google Scholar 

  11. A. Dhakshinamoorthy, H. Garcia, Chem. Soc. Rev. 41(15), 5262 (2012). https://doi.org/10.1039/c2cs35047e

    Article  CAS  PubMed  Google Scholar 

  12. M.R. Buchmeiser (ed.), Polymeric materials in organic synthesis and catalysis (Wiley Interscience, Weinheim, 2005)

    Google Scholar 

  13. A. Taguchi, F. Schüth, Micropor. Mesopor. Mat. 77(1), 1–45 (2005). https://doi.org/10.1016/j.micromeso.2004.06.030

    Article  CAS  Google Scholar 

  14. S. Sabater, J.A. Mata, E. Peris, ACS Catal. 4(6), 2038–2204 (2014). https://doi.org/10.1021/cs5003959

    Article  CAS  Google Scholar 

  15. J.M. Fraile, J.I. García, J.A. Mayoral, Chem. Rev. 109(2), 360–417 (2009). https://doi.org/10.1021/cr800363y

    Article  CAS  PubMed  Google Scholar 

  16. J. Lu, P.H. Toy, Chem. Rev. 109(2), 815–838 (2009). https://doi.org/10.1021/cr8004444

    Article  CAS  PubMed  Google Scholar 

  17. B.M.L. Dioos, I.F.J. Vankelecom, P.A. Jacobs, Adv. Synth. Catal. 348(12–13), 1413–1446 (2006). https://doi.org/10.1002/adsc.200606202

    Article  CAS  Google Scholar 

  18. B. Altava, M.I. Burguete, J.M. Fraile, J.I. García, S.V. Luis, J.A. Mayoral, M.J. Vicent, Angew. Chem. Int. Ed. 39(8), 1503–1506 (2000). https://doi.org/10.1002/(sici)1521-3773(20000417)39:8%3c1503::aid-anie1503%3e3.0.co;2-b

    Article  CAS  Google Scholar 

  19. J.T. Ayres, C.K. Mann, J. Polym. Sci., Part B: Polym. Lett. 3(6), 505–508 (1965). https://doi.org/10.1002/pol.1965.110030617

  20. K.S. Devaky, V.R. Pillai, Eur. Polym. J. 24(3), 209–213 (1988). https://doi.org/10.1016/0014-3057(88)90210-8

    Article  CAS  Google Scholar 

  21. R. Slimi, R.B. Othman, N. Sleimi, A. Ouerghui, C. Girard, Polymers 8, 187 (2016). https://doi.org/10.3390/polym8050187

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. S. Chacko, T. Mathew, S. Kuriakose, J. Appl. Polym. Sci. 90(10), 2684–2690 (2003). https://doi.org/10.1002/app.12921

    Article  CAS  Google Scholar 

  23. A.H. Ahmed, Chem. Inform. 46(34) (2015). https://doi.org/10.1002/chin.20153425

  24. D. Kılınç, Ö. Şahin, Int. J. Hydrog. Energy 43(23), 10717–10727 (2018). https://doi.org/10.1016/j.ijhydene.2018.02

    Article  Google Scholar 

  25. H. Zhang, B. Xu, L. Zhou, Z.M. Zhang, J. Zhang, Green Synth. Catal. (2023). https://doi.org/10.1016/j.gresc.2023.04.002

    Article  Google Scholar 

  26. D.P. Zhuchkov, M.V. Nenasheva, M.V. Terenina, Y.S. Kardasheva, D.N. Gorbunov, E.A. Karakhanov, Pet. Chem. 61(1), 1–14 (2020). https://doi.org/10.1134/s0965544121010011

    Article  CAS  Google Scholar 

  27. P.C. Selvaraj, V. Mahadevan, J. Mol. Catal. A: Chem. 120(1–3), 47–54 (1997). https://doi.org/10.1016/s1381-1169(96)00422-0

    Article  CAS  Google Scholar 

  28. T.S. Reger, K.D. Janda, J. Am. Chem. Soc. 122(29), 6929–6934 (2000). https://doi.org/10.1021/ja000692r

    Article  CAS  Google Scholar 

  29. M. Islam, D. Hossain, P. Mondal, K. Tuhina, A.S. Roy, S. Mondal, Trans. Met. Chem. 36, 223–230 (2011). https://doi.org/10.1007/s11243-011-9459-1

    Article  CAS  Google Scholar 

  30. S. Sharma, S. Sinha, S. Chand, Ind. Eng. Chem. Res. 51, 8806–8814 (2012). https://doi.org/10.1021/ie201953y

    Article  CAS  Google Scholar 

  31. M. Islam, S. Mondal, P. Mondal, A.S. Roy, K. Tuhina, Catal. Lett. 141, 1171–1181 (2011). https://doi.org/10.1007/s10562-011-0606-2

    Article  CAS  Google Scholar 

  32. A. Maurya, N. Kesharwani, P. Kachhap, V.K. Mishra, N. Chaudhary, Appl. Organomet. Chem. 33, e5094 (2019). https://doi.org/10.1002/aoc.5094

    Article  CAS  Google Scholar 

  33. V.B. Valodkar, G.L. Tembe, M. Ravindranathan, R.N. Ram, J. Mol. Catal. A: Chem. 208, 21–32 (2004). https://doi.org/10.1016/j.molcata.2003.07.001

    Article  CAS  Google Scholar 

  34. Z. Dehbanipour, M. Moghadam, S. Tangestaninejad, V. Mirkhani, Appl. Organomet. Chem. 32, e4436 (2018) .https://doi.org/10.1002/aoc.4436

  35. S.M. Islam, S. Mondal, P. Mondal, A.S. Roy, K. Tuhina, J. Organomet. Chem.. 696, 4264–4274 (2012). https://doi.org/10.1016/j.jorganchem.2011.10.004

    Article  CAS  Google Scholar 

  36. M. Islam, S. Mondal, M. Manir, A. Singha Roy, P. Mondal, Chin. J. Chem. 28 , 1810–1820 (2010). https://doi.org/10.1002/cjoc.201090304

  37. S.M. Islam, N. Salam, P. Mondal, A.S. Roy, J. Mol. Catal. A: Chem. 387, 7–19 (2014). https://doi.org/10.1016/j.molcata.2014.02.007

    Article  CAS  Google Scholar 

  38. M. Tilliet, S. Lundgren, C. Moberg, Adv. Synth. Catal. 349, 2079–2084 (2007). https://doi.org/10.1002/adsc.200700112

    Article  CAS  Google Scholar 

  39. B. Movassagh, N. Rezaei, Tetrahedron 70, 8885–8892 (2014). https://doi.org/10.1016/j.tet.2014.09.092

    Article  CAS  Google Scholar 

  40. L. Harmand, P. Drabina, V. Pejchal, L. Husáková, Tetrahedron Lett. 56, 6240–6243 (2015) https://doi.org/10.1016/j.tetlet.2015.09.112

  41. G. Nováková, P. Drabina, B. Frumarová, M. Sedlák, Adv. Synthe. Catal. 358, 2541–2552 (2016). https://doi.org/10.1002/adsc.20160019

    Article  Google Scholar 

  42. M. Nasrollahzadeh, A. Zahraei, E. Pourbasheer, Monats. für Chem. 146 , 1329–1334 (2015). 0.1007/s00706–014–1367–6

  43. A. Bukowska, W. Bukowski, K. Bester, Appl. Organomet. Chem. 31, e3847 (2017). https://doi.org/10.1002/aoc.3847

    Article  CAS  Google Scholar 

  44. M.R. Maurya, S. Sikarwar, T. Joseph, S.B. Halligudi, J. Mol. Catal. A: Chem. 236, 132–138 (2005). https://doi.org/10.1016/j.molcata.2005.02.034

    Article  CAS  Google Scholar 

  45. N. Rezaei, B. Movassagh, Tetrahedron Lett. 57, 1625–1628 (2016). https://doi.org/10.1016/j.tetlet.2016.03.005

    Article  CAS  Google Scholar 

  46. S. Yan, S. Pan, T. Osako, Y. Uozumi, Synlett 27, 1232–1236 (2016). https://doi.org/10.1055/s-0035-1561361;ArtID:st-2015-d0963-l

    Article  CAS  Google Scholar 

  47. B. Kodicherla, P.C. Perumgani, M.R. Mandapati, Appl. Organomet. Chem. 28, 756–759 (2014). https://doi.org/10.1002/aoc.3193

    Article  CAS  Google Scholar 

  48. P.C. Perumgani, S. Keesara, S. Parvathaneni, M.R. Mandapati, New J. Chem. 40, 5113–5120 (2016). https://doi.org/10.1039/x0xx00000x

    Article  CAS  Google Scholar 

  49. A. Mandoli, R. Garzelli, S. Orlandi, D. Pini, M. Lessi, Catal. Today 140, 51–57 (2009). https://doi.org/10.1016/j.cattod.2008.07.007

    Article  CAS  Google Scholar 

  50. L. Maestre, E. Ozkal, C. Ayats, Á. Beltrán, M.M. Díaz-Requejo, P.J. Pérez, Chem. Sci. 6, 1510–1515 (2015). https://doi.org/10.1039/c4sc03277b

    Article  CAS  PubMed  Google Scholar 

  51. L. Wang, C. Huang, C. Cai, Catal. Commun. 11, 532–536 (2010). https://doi.org/10.1016/j.catcom.2009.12.012

    Article  CAS  Google Scholar 

  52. H. F. Jiang, A. Z. Wang, H. L. Liu, 2309–2312 (2008). https://doi.org/10.1002/ejoc.200701165

  53. M.R. Rodríguez, F. Molina, P. Etayo, M.A. Pericàs, P.J. Pérez, Europ. J. Inorg. Chem. 36, 3727–3730 (2021). https://doi.org/10.1002/ejic.202100526

    Article  CAS  Google Scholar 

  54. M.M. Islam, A.S. Roy, S.M. Islam, Catal. Lett. 146, 1128–1138 (2016). https://doi.org/10.1007/s10562-016-1728-3

    Article  CAS  Google Scholar 

  55. T. Erkenez, M. Tümer, Arab. J. Chem. 12, 2618–2631 (2019). https://doi.org/10.1016/j.arabjc.2015.04.026

    Article  CAS  Google Scholar 

  56. R. Slimi, R. Ben Othman, N. Sleimi, A. Ouerghui, Polymers. 8, 187 (2016). https://doi.org/10.3390/polym8050187

  57. J. Wang, J. Li, Y. Wang, S. He, H. You, F.E. Chen, ACS Catal. 12, 9629–9637 (2022). https://doi.org/10.1021/acscatal.2c02056

    Article  CAS  Google Scholar 

  58. J. Song, K. Zhang, Z. Huang, J. Zhao, Z. Yang, L. Zong, Catal. Sci. Technol. 12, 722–727 (2022). https://doi.org/10.1039/D1CY02002A

    Article  CAS  Google Scholar 

  59. L. Bahsis, B. El. Ayouchia, H. Pascual‐Álvarez, A.De Munno, G. Julve, Appl. Organomet. Chem. 33, e4669 (2019). https://doi.org/10.1002/aoc.4669

  60. V.N. Mikhailov, K. Korvinson, V.N. Sorokoumov, Russ. J. Gen. Chem. 86, 2473–2476 (2016). https://doi.org/10.1134/S1070363216110128

    Article  CAS  Google Scholar 

  61. E. Mohammadi, B. Movassagh, J. Mol. Catal. A: Chem. 418, 158–167 (2016). https://doi.org/10.1016/j.molcata.2016.03.045

    Article  CAS  Google Scholar 

  62. M. Bakherad, A. Keivanloo, B. Bahramian, J. Braz. Chem. Soc. 20, 907–912 (2009). https://doi.org/10.1590/S0103-50532009000500015

    Article  CAS  Google Scholar 

  63. V. Udayakumar, S. Alexander, V. Gayathri, K.R. Patil, J. Mol. Catal. A: Chem. 317, 111–117 (2010). https://doi.org/10.1016/j.molcata.2009.10.030

    Article  CAS  Google Scholar 

  64. Q. Meng, H. Zhang, H. Chen, Q. Teng, ChemistrySelect 6, 5375–5380 (2021). https://doi.org/10.1002/slct.202100968

    Article  CAS  Google Scholar 

  65. S. Alexander, V. Udayakumar, V. Gayathri, J. Mol. Catal. A: Chem. 314, 21–27 (2009). https://doi.org/10.1016/j.molcata.2009.08.012

    Article  CAS  Google Scholar 

  66. Y. He, C. Cai, Catal. Lett. 140, 153–159 (2010). https://doi.org/10.1007/s10562-010-0415-z

    Article  CAS  Google Scholar 

  67. S.M. Islam, R.A. Molla, A.S. Roy, K. Ghosh, RSC Adv. 4, 26181–26192 (2014). https://doi.org/10.1039/C4RA03338H

    Article  CAS  Google Scholar 

  68. T.K. Dey, P. Basu, S. Riyajuddin, A. Ghosh, K. Ghosh, S.M. Islam, New J. Chem. 43, 9802–9814 (2019). https://doi.org/10.1039/C9NJ01786K

    Article  CAS  Google Scholar 

  69. S.M. Islam, P. Mondal, K. Tuhina, A.S. Roy, S. Mondal, Inorg. Organomet. Polym. Mater. 20, 264–277 (2010). https://doi.org/10.1007/s10904-010-9352-y

    Article  CAS  Google Scholar 

  70. R. Antony, G.L. Tembe, M. Ravindranathan, J. Appl. Polym. Sci. 90, 370–378 (2003). https://doi.org/10.1002/app.12587

    Article  CAS  Google Scholar 

  71. J.H. Kim, J.W. Kim, M. Shokouhimehr, J. Org. Chem. 70, 6714–6720 (2005). https://doi.org/10.1021/jo050721m

    Article  CAS  PubMed  Google Scholar 

  72. K. Hallman, E. Macedo, K. Nordström, Tetrahedron: Asymmetry. 10, 4037–4046 (1999). https://doi.org/10.1016/S0957-4166(99)00416-4

  73. C.P. Perumgani, S.P. Parvathaneni, B. Kodicherla, S. Keesara, Inorganica Chimi. Acta. 455, 105–111 (2017). https://doi.org/10.1016/j.ica.2016.10.014

    Article  CAS  Google Scholar 

  74. B. Zhang, Z. Ye, M. Qin, Q. Wang, Y. Du, J. Appl. Polym. Sci. 138, 49666 (2021). https://doi.org/10.1002/app.49666

    Article  CAS  Google Scholar 

  75. W.J. Zhou, K.H. Wang, J.X. Wang, D.F. Huang, 416–419 (2010). https://doi.org/10.1002/ejoc.200901210

  76. E. Alacid, C. Nájera, Arkivoc, 8(2008). https://doi.org/10.3998/ark.5550190.0009.806

  77. S. Schweizer, J.M. Becht, C. Le Drian, Adv. Synthe. Catal. 34, 1150–1158 (2007). https://doi.org/10.1002/adsc.200600503

    Article  CAS  Google Scholar 

  78. S. George, K. Sreekumar, Appl. Organomet. Chem. 35, e6083 (2021). https://doi.org/10.1002/aoc.6083

    Article  CAS  Google Scholar 

  79. E. Mohammadi, B. Movassagh, New J. Chem. 42, 11471–11479 (2018). https://doi.org/10.1039/C8NJ01042K

    Article  CAS  Google Scholar 

  80. W. Mansour, M. Fettouhi, Q. Saleem, Appl. Organomet. Chem. 35, e6195 (2021). https://doi.org/10.1002/aoc.6195

    Article  CAS  Google Scholar 

  81. K. Yamamoto, R. Nameki, H. Sogawa, T. Takata, Tetrahedron Lett. 61, 151870 (2020). https://doi.org/10.1016/j.tetlet.2020.151870

    Article  CAS  Google Scholar 

  82. N.A.M. Shamsuddin, N.A.A. Rahman, K. Chandrasekaram, Y. Alias, Malay. J. Anal. Sci. 25, 987–997 (2021)

    Google Scholar 

  83. D. Sciosci, F. Valentini, F. Ferlin, S. Chen, Y. Gu, O. Piermatti, Green Chem. 22, 6560–6566 (2020). https://doi.org/10.1039/D0GC02634D

    Article  CAS  Google Scholar 

  84. M.J. Madhura, A.S. Jeevan Chakravarthy, S. Hariprasad, V. Gayathri, Catal. Lett. 1–9 (2022). https://doi.org/10.1007/s10562-022-04055-7

  85. G. Shi, Z. Dong, Molecules. 27 , 4777 (2022) https://doi.org/10.3390/molecules27154777

  86. S. M. Lakshminarayana, R. Boregowda, G. Virupaiah, Chem. Papers. 1–13 (2023). https://doi.org/10.1007/s11696-023-02721-7

  87. M.R. Maurya, B. Uprety, N. Chaudhary, F. Avecilla, Inorganica Chim. Acta. 434, 230–238 (2015). https://doi.org/10.1016/j.ica.2015.05.027

    Article  CAS  Google Scholar 

  88. M.R. Maurya, N. Chaudhary, F. Avecilla, J. Inorg. Biochem. 147, 181–192 (2015). https://doi.org/10.1016/j.jinorgbio.2015.01.012

    Article  CAS  PubMed  Google Scholar 

  89. S.M. Islam, A.S. Roy, P. Mondal, J. Mol. Catal. A: Chem. 358, 38–48 (2012). https://doi.org/10.1016/j.molcata.2012.02.009

    Article  CAS  Google Scholar 

  90. V.K. Singh, A. Maurya, N. Kesharwani, P. Kachhap, S. Kumari, Coord. Chem. 71, 520–541 (2018). https://doi.org/10.1080/00958972.2018.1434516

    Article  CAS  Google Scholar 

  91. M.K. Renuka, V. Gayathri, Catal. lett. 149, 1266 (2019). https://doi.org/10.1007/s10562-019-02710-0

    Article  CAS  Google Scholar 

  92. N. Kesharwani, N. Chaudhary, C. Haldar, Catal. Lett. 1–20 (2021). https://doi.org/10.1007/s10562-021-03594-9

  93. M.R. Maurya, A. Chauhan, S. Arora, P. Gupta, Catal. Today 3, 397–399 (2022). https://doi.org/10.1016/j.cattod.2022.03.006

    Article  CAS  Google Scholar 

  94. N. Kesharwani, N. Chaudhary, C. Haldar, Catal. Today 397, 604–617 (2022). https://doi.org/10.1016/j.cattod.2021.06.005

    Article  CAS  Google Scholar 

  95. M.R. Maurya, A. Patter, D. Singh, K. Ghosh, Catalysts 13(2), 234 (2023). https://doi.org/10.3390/catal13020234

    Article  CAS  Google Scholar 

  96. M.R. Maurya, M. Nandi, A. Patter, F. Avecilla, K. Ghosh, Catalysts 13(3), 615 (2023). https://doi.org/10.3390/catal1303061

    Article  CAS  Google Scholar 

  97. E.R. Shilpa, V. Gayathri, J. Saudi Chem. Soc. 22, 678–691 (2018). https://doi.org/10.1016/j.jscs.2017.12.004

    Article  CAS  Google Scholar 

  98. S.E. Rao, V. Gayathri, J. Appl. Polym. Sci. 135, 464800 (2018). https://doi.org/10.1002/app.46480

    Article  CAS  Google Scholar 

  99. R. Khatun, S. Biswas, S. Ghosh, S.M. Islam, J. Organomet. Chem. 858, 37–46 (2018). https://doi.org/10.1016/j.jorganchem.2018.01.001

    Article  CAS  Google Scholar 

  100. N. Nath, H.C. Pradhan, T. Maharana, A.K. Sutar, Int. J. Chem. Eng. 8, 127 (2017). https://doi.org/10.18178/ijcea.2017.8.2.643

    CAS  Google Scholar 

  101. A.K. Sutar, Y. Das, S. Pattanaik, A. Routaray, Am. J. Appl. Chem. 1, 28–36, (2013). https://doi.org/10.11648/j.ajac.20130102.13

  102. S. Islam, K. Ghosh, A.S. Roy, N. Salam, J. Inorg. Organomet. Polym. and Mater. 24, 457–467 (2014). https://doi.org/10.1007/s10904-013-0017-5]

    Article  CAS  Google Scholar 

  103. P. Basu, T.K. Dey, A. Ghosh, S.M. Islam, J. Inorg. Organomet. Polym. Matter 28, 1158–1170 (2018). https://doi.org/10.1007/s10904-018-0785-z

    Article  CAS  Google Scholar 

  104. B. Martín-Matute, S.I. Pereira, E. Peña-Cabrera, J. Adrio, A.M. Silva, Adv. Synth. Catal. 349, 1714–1724 (2007). https://doi.org/10.1002/adsc.200600647

    Article  CAS  Google Scholar 

  105. N. Taheri, M. Fallah-Mehrjardi, S. Sayyahi, Bull. Chem. Soc. Ethiop. 32, 531–540 (2018). https://doi.org/10.4314/bcse.v32i3.12

    Article  CAS  Google Scholar 

  106. O. Belda, S. Lundgren, C. Moberg, Org. Lett. 5, 2275–2278 (2003). https://doi.org/10.1021/ol034605m

    Article  CAS  PubMed  Google Scholar 

  107. J.J. Boruah, S.P. Das, RSC Adv. 8, 34491–34504 (2018). https://doi.org/10.1039/C8RA05969A

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  108. K. Arashiba, T. Itabashi, K. Nakajima, Y. Nishibayashi, Chem. Lett. 48, 693–695 (2019). https://doi.org/10.1246/cl.190193

    Article  CAS  Google Scholar 

  109. M.R. Maurya, A. Chauhan, A. Verma, U. Kumar, Catal. Today 388, 274–287 (2022). https://doi.org/10.1016/j.cattod.2020.06.031

    Article  CAS  Google Scholar 

  110. M.R. Maurya, A. Chauhan, Top. Catal. 1–15 (2022). https://doi.org/10.1007/s11244-022-01747-7

  111. G. Grivani, A. Halili, J. Iran. Chem. Soc. 11, 163–168 (2014). https://doi.org/10.1007/s13738-013-0286-5

    Article  CAS  Google Scholar 

  112. G. Grivani, N. Gholampoor, J. Iran. Chem. Soc. 9, 349–355 (2012). https://doi.org/10.1007/s13738-011-0030-y

    Article  CAS  Google Scholar 

  113. M. R. Maurya, A. Patter, A. Chauhan, N. Kumar, Top Catal. 1–17 (2023). https://doi.org/10.1007/s11244-023-01861-0

  114. K. Takeda, T. Oohara, M. Anada, H. Nambu, Angew. Chem.. 122, 7133–7137 (2010). https://doi.org/10.1002/anie.201003730

    Article  CAS  Google Scholar 

  115. C. Bianchini, M. Frediani, G. Mantovani, F. Vizza, Organometallics 20, 2660–2662 (2001). https://doi.org/10.1021/om0010868

    Article  CAS  Google Scholar 

  116. C. Bianchini, M. Frediani, F. Vizza, Chem. Commun. 5, 479–480 (2001). https://doi.org/10.1039/b010128l

    Article  Google Scholar 

  117. C. Yan, X. Zeng, W. Zhang, M. Luo, J. Organomet. Chem. 691, 3391–3396 (2006). https://doi.org/10.1016/j.jorganchem.2006.02.021

    Article  CAS  Google Scholar 

  118. V. Gayathri, Indian J. Chem.-Section A (IJCA), 58, 964 971(2020). https://doi.org/10.56042/ijca.v58i9.23704

  119. S.M. Islam, A.S. Roy, S. Dalapati, P. Mondal, J. Mol. Catal. A: Chem. 380, 94–103 (2013). https://doi.org/10.1016/j.molcata.2013.09.022

    Article  CAS  Google Scholar 

  120. D. Lončarević, J. Krstić, J. Dostanić, D. Manojlović, Chem. Eng. J. 157, 181–188 (2010). https://doi.org/10.1016/j.cej.2009.11.034

    Article  CAS  Google Scholar 

  121. P. Goyal, X. Zheng, M. Weck, Adv. Synth. Catal. 350, 1816–1822 (2008). https://doi.org/10.1002/adsc.200800175

    Article  CAS  Google Scholar 

  122. S. Chand, S. Sinha, J. Appl. Polym. Sci. 130, 2127–2135 (2013). https://doi.org/10.1002/app.39374

    Article  CAS  Google Scholar 

  123. T.K. Dey, K. Ghosh, P. Basu, R.A. Molla, S.M. Islam, New J. Chem. 42, 9168–9176 (2018). https://doi.org/10.1039/C8NJ00475G

    Article  CAS  Google Scholar 

  124. Y. Oe, Y. Uozumi, Adv. Synth. Catal. 350, 1771–1775 (2008). https://doi.org/10.1002/adsc.200800359

    Article  CAS  Google Scholar 

  125. M. Moghadam, V. Mirkhani, S. Tangestaninejad, I. Mohammadpoor-Baltork, H. Kargar, I. Sheikhshoaei, J. Iran. Chem. Soc. 8, 1019–1029 (2011). https://doi.org/10.1007/BF03246558

    Article  CAS  Google Scholar 

  126. S. Mujahed, F. Valentini, S. Cohen, L. Vaccaro, Chemsuschem 12, 4693–4699 (2019). https://doi.org/10.1002/cssc.201901728

    Article  CAS  PubMed  Google Scholar 

  127. V.A. Larionov, T. Cruchter, T. Mietke, Organometallics 36, 1457–1460 (2017). https://doi.org/10.1021/acs.organomet.7b00016

    Article  CAS  Google Scholar 

  128. C.A. Smith, F. Brandi, M. Al-Naji, R. Guterman, RSC Adv. 11, 15835–15840 (2021). https://doi.org/10.1039/D1RA01460A

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  129. R. Liu, S.C. Cheng, Y. Xiao, K.C. Chan, K.M. Tong, C.C. Ko, J. Catal. 407, 206–212 (2022). https://doi.org/10.1016/j.jcat.2022.01.024

    Article  CAS  Google Scholar 

  130. J.H. Rigby, M.A. Kondratenko, Org. Lett. 2, 3917–3919 (2000). https://doi.org/10.1021/ol0002931

    Article  CAS  PubMed  Google Scholar 

  131. S. Biswas, R. Khatun, M. Sengupta, S.M. Islam, Mol. Catal. 452, 129–137 (2018). https://doi.org/10.1016/j.mcat.2018.04.009

    Article  CAS  Google Scholar 

  132. A. Rahmatpour, R. Emen, G. Amini, J. Organomet. Chem. 892, 24–33 (2019). https://doi.org/10.1016/j.jorganchem.2019.04.004

    Article  CAS  Google Scholar 

  133. T.K. Dey, K. Ghosh, P. Basu, J. Appl. Polym. Sci. 136, 47650 (2019). https://doi.org/10.1002/app.47650

    Article  CAS  Google Scholar 

  134. K. Gauli, R.N. Ram, H.P. Soni, J. Mol. Catal. A: Chem. 242, 161–167 (2005). https://doi.org/10.1016/j.molcata.2005.07.014

    Article  CAS  Google Scholar 

  135. S. Lundgren, S. Lutsenko, C. Jönsson, C. Moberg, Org. Lett. 5, 3663–3665 (2003). https://doi.org/10.1021/ol0353363

    Article  CAS  PubMed  Google Scholar 

  136. G. Sourkouni-Argirusi, A. Kirschning, Org. Lett. 2, 3781–3784 (2000). https://doi.org/10.1021/ol006483t

    Article  CAS  PubMed  Google Scholar 

  137. J.P. Patel, J.R. Avalani, D.K. Raval, J. Chem. Sci. 125, 531–536 (2013). https://doi.org/10.1007/s12039-013-0408-8

    Article  CAS  Google Scholar 

  138. P. Patil, A. Yadav, L. Bavkar, B.N. Nippu, N.D. Satyanarayan, J. Mol. Struct. 1242, 130672 (2021). https://doi.org/10.1016/j.molstruc.2021.130672

    Article  CAS  Google Scholar 

  139. B.J. Khairnar, D.V. Mane, B.R. Chaudhari, J. Appl. Chem. 8, 425–434 (2019)

    CAS  Google Scholar 

  140. M. Aguilar-MartÝnez, J.T. Vargas-Durazo, A. Ochoa-Terßn, H. Santacruz-Ortega, K. Ochoa-Lara, A. Zizumbo-Lˇpez, Tetrahedron 91, 132195 (2021). https://doi.org/10.1016/j.tet.2021.132195

    Article  CAS  Google Scholar 

  141. M. Fantinel, N. Valiati, P.A. Moro, Tetrahedron 86, 132081 (2021). https://doi.org/10.1016/j.tet.2021.132081

    Article  CAS  Google Scholar 

  142. H. Kargar, M. Moghadam, L. Shariati, N. Feizi, J. Iran. Chem. Soc. 19(7), 3067–3077 (2022). https://doi.org/10.1007/s13738-022-02517-8

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors are thankful to the Maharishi Markandeshwar (Deemed to be University), Mullana, Haryana, India.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Sunil Kumar, Ravindra K. Rawal or Praveen Kumar Gupta.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kumari, S., Kumar, S., Karan, R. et al. Synthetic and catalytic perspectives of polystyrene supported metal catalyst. J IRAN CHEM SOC 21, 951–1010 (2024). https://doi.org/10.1007/s13738-024-02970-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13738-024-02970-7

Keywords

Navigation