Abstract
An efficient and recyclable Pd nano-catalyst was developed via immobilization of Pd nanoparticles on polyimide linked covalent organic frameworks (PCOFs) that was facilely prepared through condensation of melamine and 3,3′,4,4′-biphenyltetracarboxylic dianhydride. The Pd nanoparticles (Pd NPs) catalyst was thoroughly characterized by FT-IR, XRD, SEM, TEM. Furthermore, the catalytic activity of Pd NPs catalyst was evaluated by Suzuki–Miyaura coupling reaction and nitroarene reduction in water, respectively. The excellent yields of corresponding products revealing revealed that the Pd NPs catalyst could be applied as an efficient and reusable heterogeneous catalyst for above two reactions.
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Hulsey MJ, Lim CW, Yan N (2020) Chem Sci 11:1456–1468
Li Z, Ji SF, Liu YW, Cao X, Tian SB, Chen YJ, Niu ZG, Li YD (2020) Chem Rev 120:623–682
Molnár Á, Papp A (2017) Coord Chem Rev 349:1–65
Karimi B, Mansouri F, Mirzaei HM (2015) ChemCatChem 7:1736–1789
Gao YX, Ding Y (2020) Chemistry-a European Journal 26:8845–8856
Gholinejad M, Naghshbandi Z, Najera C (2019) ChemCatChem 11:1792–1823
Hong K, Sajjadi M, Suh JM, Zhang K, Nasrollahzadeh M, Jang HW, Varma RS, Shokouhimehr M (2020) ACS Applied Nano Materials 3:2070–2103
Shokouhimehr, Yek, Nasrollahzadeh (2019) Appl. Sci. 9:4183.
Kim A, Rafiaei SM, Abolhosseini S, Shokouhimehr M (2015) Energy Environ Focus 4:18–23
Shokouhimehr M, Asl MS, Mazinani B (2017) Res Chem Intermed 44:1617–1626
Zhang K, Hong K, Suh JM, Lee TH, Kwon O, Shokouhimehr M, Jang HW (2018) Res Chem Intermed 45:599–611
Yang X-F, Wang A, Qiao B, Li J, Liu J, Zhang T (2013) Acc Chem Res 46:1740–1748
Zhang H, Liu G, Shi L, Ye J (2018) Adv Energy Mater 8:1701343
Liu L, Corma A (2018) Chem Rev 118:4981–5079
Dong ZH, Yuan JW, Xiao YM, Mao P, Wang WT (2018) J Org Chem 83:11067–11073
Liu Y-X, Ma Z-W, Jia J, Wang C-C, Huang M-L, Tao J-C (2010) Appl Organomet Chem 24:646–649
Motevalizadeh SF, Alipour M, Ashori F, Samzadeh-Kermani A, Hamadi H, Ganjali MR, Aghahosseini H, Ramazani A, Khoobi M, Gholibegloo E (2018) Appl Organomet Chem 32:e4123
Khajehzadeh M, Moghadam M (2018) J Organomet Chem 863:60–69
Waller PJ, Gandara F, Yaghi OM (2015) Acc Chem Res 48:3053–3063
Ding SY, Wang W (2013) Chem Soc Rev 42:548–568
Feng X, Ding X, Jiang D (2012) Chem Soc Rev 41:6010–6022
Kandambeth S, Dey K, Banerjee R (2019) J Am Chem Soc 141:1807–1822
Gao X, Zou X, Ma H, Meng S, Zhu G (2014) Adv Mater 26:3644–3648
Fang Q, Wang J, Gu S, Kaspar RB, Zhuang Z, Zheng J, Guo H, Qiu S, Yan Y (2015) J Am Chem Soc 137:8352–8355
Guo J, Jiang D (2020) ACS Cent Sci 6:869–879
Wu C, Liu Y, Liu H, Duan C, Pan Q, Zhu J, Hu F, Ma X, Jiu T, Li Z, Zhao Y (2018) J Am Chem Soc 140:10016–10024
Liu R, Tan KT, Gong Y, Chen Y, Li Z, Xie S, He T, Lu Z, Yang H, Jiang D (2021) Chem Soc Rev 50:120–242
Niakan M, Masteri-Farahani M, Karimi S, Shekaari H (2021) J Mol Liq 324:115078
Niakan M, Asadi Z, Masteri-Farahani M (2019) ChemistrySelect 4:1766–1775
Huang P, Zeng X, Du F, Zhang L, Peng X (2019) Catal Lett 150:1011–1019
Hooshmand SE, Heidari B, Sedghi R, Varma RS (2019) Green Chem 21:381–405
Han Y, Di JQ, Zhao AD, Zhang ZH (2019) Appl Organomet Chem 33:e5172
Antony R, Marimuthu R, Murugavel R (2019) ACS Omega 4:9241–9250
Chakraborty S, Mruthunjayappa MH, Aruchamy K, Singh N, Prasad K, Kalpana D, Ghosh D, Sanna Kotrappanavar N, Mondal D (2019) ACS Sustain Chem Eng 7:14225–14235
Uberman PM, García CS, Rodríguez JR, Martín SE (2017) Green Chem 19:739–748
Du J, Chen J, Xia H, Zhao Y, Wang F, Liu H, Zhou W, Wang B (2020) ChemCatChem 12:2426–2430
Wang G, Yuan S, Wu ZQ, Liu WY, Zhan HJ, Liang YP, Chen XY, Ma BJ, Bi SX (2019) Appl Organomet Chem 33:e5159
Jiang L, Tian Y, Sun T, Zhu Y, Ren H, Zou X, Ma Y, Meihaus KR, Long JR, Zhu G (2018) J Am Chem Soc 140:15724–15730
Han Y, Zhang M, Zhang Y-Q, Zhang Z-H (2018) Green Chem 20:4891–4900
Rangel Rangel E, Maya EM, Sánchez F, de la Campa JG, Iglesias M (2015) Green Chem 17:466–473
Acknowledgements
The authors are grateful to the Doctor Fund of Henan University of Technology (No. 2015BS013) and The Colleges and Universities Key Research Program Foundation of Henan Province (No. 20A150014). The Project was also Supported by State Key Laboratory of Materials Processing and Die & Mould Technology, Huazhong University of Science and Technology (P2019-004)
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Dong, Z., Pan, H., Gao, P. et al. Palladium Immobilized on a Polyimide Covalent Organic Framework: An Efficient and Recyclable Heterogeneous Catalyst for the Suzuki–Miyaura Coupling Reaction and Nitroarene Reduction in Water. Catal Lett 152, 299–306 (2022). https://doi.org/10.1007/s10562-021-03637-1
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DOI: https://doi.org/10.1007/s10562-021-03637-1