Switching of support materials for the hydrogenation of nitroarenes: A review

References

• Mitsudome, T.; Kaneda, K. Gold Nanoparticle Catalysts for Selective Hydrogenations. Green Chem. 2013, 15, 2636–2654.
   Web of Science ®Google Scholar
• Lara, P.; Philippot, K. The Hydrogenation of Nitroarenes Mediated by Platinum Nanoparticles: An Overview. Catal. Sci. Technol. 2014, 4(8), 2445–2465. DOI: 10.1039/C4CY00111G.
   Web of Science ®Google Scholar
• Nozawa-Kumada, K.; Abe, E.; Ito, S.; Shigeno, M.; Kondo, Y. Super Electron Donor-mediated Reductive Transformation of Nitrobenzenes: A Novel Strategy to Synthesize Azobenzenes and Phenazines. Org. Biomol. Chem. 2018, 16(17), 3095–3098. DOI: 10.1039/C8OB00271A.
   PubMed Web of Science ®Google Scholar
• Downing, R. S.; Kunkeler, P. J.; Van Bekkum, H. Catalytic Syntheses of Aromatic Amines. Catal. Today. 1997, 37(2), 121–136. DOI: 10.1016/S0920-5861(97)00005-9.
   Web of Science ®Google Scholar
• Wegener, G.; Brandt, M.; Duda, L.; Hofmann, J.; Klesczewski, B.; Koch, D.; Kumpf, R. J.; Orzesek, H.; Pirkl, H. G.; Six, C, et al. Trends in Industrial Catalysis in the Polyurethane Industry. Appl. Catal., A. 2001, 221(1–2), 303–335. DOI: 10.1016/S0926-860X(01)00910-3.
   Web of Science ®Google Scholar
• El-Hout, S. I.; El-Sheikh, S. M.; Hassan, H. M.; Harraz, F. A.; Ibrahim, I. A.; El-Sharkawy, E. A. A Green Chemical Route for Synthesis of Graphene Supported Palladium Nanoparticles: A Highly Active and Recyclable Catalyst for Reduction of Nitrobenzene. Appl. Catal., A. 2015, 503, 176–185.
   Web of Science ®Google Scholar
• Wang, J.; Yuan, Z.; Nie, R.; Hou, Z.; Zheng, X. Hydrogenation of Nitrobenzene to Aniline over Silica Gel Supported Nickel Catalysts. Ind. Eng. Chem. Res. 2010, 49, 4664–4669.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Manna, A. K.; Satyanarayana, G., and Subrahmanyam, C. Palladium Nanoparticles on Silica Nanospheres for Switchable Reductive Coupling of Nitroarenes. Cataly. Lett. 2020, 150, 2309–2321. DOI:10.1007/s10562-020-03127-w.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Satyanarayana, G.; Subrahmanyam, C. Bimetallic Pd–Au/TiO 2 Nanoparticles: An Efficient and Sustainable Heterogeneous Catalyst for Rapid Catalytic Hydrogen Transfer Reduction of Nitroarenes. ACS Omega. 2018, 3(10), 13065–13072. DOI: 10.1021/acsomega.8b02064.
   PubMed Web of Science ®Google Scholar
• Lakshminarayana, B.; Ashok Kumar, K. V.; Selvaraj, M.; Satyanarayana, G.; Subrahmanyam, C. PVP-PS Supported Ultra-small Pd Nanoparticles for the Room Temperature Reduction of 4-nitrophenol. J. Environ. Chem. Eng. 2020, 8(4), 103899. DOI: 10.1016/j.jece.2020.103899.
   Web of Science ®Google Scholar
• Amanchi, S. R.; Kumar, K. A.; Lakshminarayana, B.; Satyanarayana, G.; Subrahmanyam, C. Photocatalytic Hydrogenation of Nitroarenes: Supporting Effect of CoO x on TiO 2 Nanoparticles. New J. Chem. 2019, 43(2), 748–754. DOI: 10.1039/C8NJ05260C.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Mahendar, L.; Ghosal, P.; Satyanarayana, G.; Subrahmanyam, C. Nano‐sized Recyclable PdO Supported Carbon Nanostructures for Heck Reaction: Influence of Carbon Materials. ChemistrySelect. 2017, 2, 2700–2707. DOI: 10.1002/slct.201602051.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Mahendar, L.; Ghosal, P.; Sreedhar, B.; Satyanarayana, G.; Subrahmanyam, C. Fabrication of Pd/CuFe 2 O 4 Hybrid Nanowires: A Heterogeneous Catalyst for Heck Couplings. New journal of Chemistry. 2018, 42(3), 1646–1654. DOI: 10.1039/C7NJ04361A.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Vinodkumar, T.; Satyanarayana, G.; Subrahmanyam, C. Novel Ultra-small Pd NPs on SOS Spheres: A New Catalyst for Domino Intramolecular Heck and Intermolecular Sonogashira Couplings. RSC Adv. 2020, 10(8), 4568–4578. DOI: 10.1039/C9RA09429F.
   PubMed Web of Science ®Google Scholar
• Lakshminarayana, B.; Mahendar, L.; Chakraborty, J.; Satyanarayana, G.; Subrahmanyam, C. Organic Transformations Catalysed by Palladium Nanoparticles on Carbon Nanomaterials. J. Chem. Sci. 2018, 130(5), 47. DOI: 10.1007/s12039-018-1449-9.
   Web of Science ®Google Scholar
• Lakshminarayana, B.; Chakraborty, J.; Satyanarayana, G.; Subrahmanyam, C. Recyclable Pd/CuFe 2 O 4 Nanowires: A Highly Active Catalyst for C–C Couplings and Synthesis of Benzofuran Derivatives. RSC Adv. 2018, 8(37), 21030–21039. DOI: 10.1039/C8RA03697G.
   PubMed Web of Science ®Google Scholar
• Dickerson, T. J.; Reed, N. N.; Janda, K. D. Soluble Polymers as Scaffolds for Recoverable Catalysts and Reagents. Chem. Rev. 2002, 102(10), 3325–3344.
   PubMed Web of Science ®Google Scholar
• Fan, Q. H.; Li, Y.-M.; Chan, A. S. C. Recoverable Catalysts for Asymmetric Organic Synthesis. Chem. Rev. 2002, 102, 3385–3466. DOI: 10.1021/cr010341a.
   PubMed Web of Science ®Google Scholar
• Van Heerbeek, R.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Dendrimers as Support for Recoverable Catalysts and Reagents. Chem. Rev. 2002, 102, 3717–3756.
   PubMed Web of Science ®Google Scholar
• Yin, L. X.; Liebscher, J. Carbon−carbon Coupling Reactions Catalysed by Heterogeneous Palladium Catalysts. Chem. Rev. 2007, 107, 133–173. DOI: 10.1021/cr0505674.
   PubMed Web of Science ®Google Scholar
• Elliott, D. C.; Hart, T. R. Catalytic Hydroprocessing of Chemical Models for Bio-oil. Energy Fuels. 2008, 23, 631–637.
   Web of Science ®Google Scholar
• Lam, E.; Luong, J. H. Carbon Materials as Catalyst Supports and Catalysts in the Transformation of Biomass to Fuels and Chemicals. ACS Catal. 2014, 4, 3393–3410. DOI: 10.1021/cs5008393.
   Web of Science ®Google Scholar
• Gawande, M. B.; Pandey, R. K.; Jayaram, R. V. Role of Mixed Metal Oxides in Catalysis Science−versatile Applications in Organic Synthesis. Catal. Sci. Technol. 2012, 2, 1113–1125.
   Web of Science ®Google Scholar
• Bond, G. C. Catalysis by Metals. Academic Press; New York. 1962, 126, 70–71.
   Google Scholar
• Tanabe, K.; Holderich, W. F. Industrial Application of Solid Acid–base Catalysts. Appl.Catal.A. 1999, 181, 399–434. DOI: 10.1016/S0926-860X(98)00397-4.
   Web of Science ®Google Scholar
• Reddy, B. M.; Khan, A. Recent Advances on TiO2−ZrO2 Mixed Oxides as Catalysts and Catalyst Supports. Catal. Rev. Sci. Eng. 2005, 47, 257–296. DOI: 10.1081/CR-200057488.
   Web of Science ®Google Scholar
• Sonavane, S. U., and Jayaram, R. V. Selective Reduction of C=O in α, β-unsaturated Carbonyls through Catalytic Hydrogen Transfer Reaction over Mixed Metal Oxides. Synlett. 2004, 2004(1), 146–148. DOI:10.1055/s-2003-43359.
   Web of Science ®Google Scholar
• Gates, B. Supported Metal Clusters: Synthesis, Structure, and Catalysis. Chem. Rev. 1995, 95;, 511–522. DOI: 10.1021/cr00035a003.
   Web of Science ®Google Scholar
• Rascon, F.; Wischert, R.; Coperet, C. Molecular Nature of Support Effects in Single-site Heterogeneous Catalysts: Silica Vs. Alumina. Chem. Sci. 2011, 2, 1449–1456. DOI: 10.1039/c1sc00073j.
   Web of Science ®Google Scholar
• Mol, J. C. Industrial Applications of Olefin Metathesis. J. Mol. Catal. A Chem. 2004, 213, 39–45. DOI: 10.1016/j.molcata.2003.10.049.
   Web of Science ®Google Scholar
• Sushko, P. V.; Mukhopadhyay, S.; Mysovsky, A. S.; Sulimov, V. B.; Taga, A.; Shluger, A. L. Structure and Properties of Defects in Amorphous Silica: New Insights from Embedded Cluster Calculations. J. Phys.: Condens. Matter. 2005, 17, S2115.
   Web of Science ®Google Scholar
• Ray, S.; Das, P.; Bhaumik, A.; Dutta, A.; Mukhopadhyay, C. Covalently Anchored Organic Carboxylic Acid on Porous Silica Nano Particle: A Novel Organometallic Catalyst (PSNP-CA) for the Chromatography-free Highly Product Selective Synthesis of Tetrasubstituted Imidazoles. Appl. Catal., A. 2013, 458, 183–195. DOI: 10.1016/j.apcata.2013.03.024.
   Web of Science ®Google Scholar
• Ray, S.; Brown, M.; Bhaumik, A.; Dutta, A.; Mukhopadhyay, C. A New MCM-41 Supported HPF 6 Catalyst for the Library Synthesis of Highly Substituted 1, 4-dihydropyridines and Oxidation to Pyridines: Report of One-dimensional Packing Towards LMSOMs and Studies on Their Photophysical Properties. Green Chem. 2013, 15, 1910–1924. DOI: 10.1039/c3gc40441b.
   Web of Science ®Google Scholar
• Kundu, P. K.; Dhiman, M.; Modak, A.; Chowdhury, A.; Polshettiwar, V.; Maiti, D. Palladium Nanoparticles Supported on Fibrous Silica (Kcc‐1‐pei/pd): A Sustainable Nanocatalyst for Decarbonylation Reactions. ChemPlusChem. 2016, 81, 1142–1146. DOI: 10.1002/cplu.201600245.
   PubMed Web of Science ®Google Scholar
• Gautam, P.; Dhiman, M.; Polshettiwar, V.; Bhanage, B. M. KCC-1 Supported Palladium Nanoparticles as an Efficient and Sustainable Nanocatalyst for Carbonylative Suzuki–Miyaura Cross-coupling. Green Chem. 2016, 18, 5890–5899. DOI: 10.1039/C6GC02012G.
   Web of Science ®Google Scholar
• Dhiman, M.; Chalke, B.; Polshettiwar, V. Efficient Synthesis of Monodisperse Metal (Rh, Ru, Pd) Nanoparticles Supported on Fibrous Nanosilica (KCC-1) for Catalysis. ACS Sustain. Chem. Eng. 2015, 3, 3224–3230. DOI 10.1021/acssuschemeng.5b00812.
   Web of Science ®Google Scholar
• Bergbreiter, D. E. Using Soluble Polymers to Recover Catalysts and Ligands. Chem. Rev. 2002, 102, 3345–3384. DOI: 10.1016/j.jcat.2006.12.011.
   PubMed Web of Science ®Google Scholar
• Dickerson, T. J.; Reed, N. N.; Janda, K. D. Soluble Polymers as Scaffolds for Recoverable Catalysts and Reagents. Chem. Rev. 2002, 102, 3325–3344. DOI 10.1021/cr010335e.
   PubMed Web of Science ®Google Scholar
• van Heerbeek, R.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Dendrimers as Support for Recoverable Catalysts and Reagents. Chem. Rev. 2002, 102, 3717–3756. DOI: 10.1021/cr0103874.
   PubMed Web of Science ®Google Scholar
• Leadbeater, N. E.; Marco, M. Preparation of Polymer-supported Ligands and Metal Complexes for Use in Catalysis. Chem. Rev. 2002, 102, 3217–3274. DOI: 10.1021/cr010361c.
   PubMed Web of Science ®Google Scholar
• McNamara, C. A.; Dixon, M. J.; Bradley, M. Recoverable Catalysts and Reagents Using Recyclable Polystyrene-based Supports. Chem. Rev. 2002, 102, 3275–3300. DOI: 10.1021/cr0103571.
   PubMed Web of Science ®Google Scholar
• Jang, S. Polymer-bound Palladium-catalysed Cross-coupling of Organoboron Compounds with Organic Halides and Organic Triflates. Tetrahedron Lett. 1997, 38, 1793. DOI: 10.1016/S0040-4039(97)00171-8.
   Google Scholar
• Ouyang, G.; Wang, C. X.; Yang, G. W. Surface Energy of Nanostructural Materials with Negative Curvature and Related Size Effects. Chem. Rev. 2009, 109, 4221–4247. DOI: 10.1021/cr900055f.
   PubMed Web of Science ®Google Scholar
• Ndolomingo, M. J.; Bingwa, N., and Meijboom, R. Review of Supported Metal Nanoparticles: Synthesis Methodologies, Advantages and Application as Catalysts. J. Mater. Sci. 2020, 55, 6195–6241. DOI:10.1007/s10853-020-04415-x.
   Web of Science ®Google Scholar
• Astruc, D.; Lu, F.; Aranzaes, J. R. Nanoparticles as Recyclable Catalysts: The Frontier between Homogeneous and Heterogeneous Catalysis. Angew. Chem. Int. Ed. 2005, 44, 7852–7872.
   PubMed Web of Science ®Google Scholar
• Polshettiwar, V.; Varma, R. S. Green Chemistry by Nanocatalysis. Green Chem. 2010, 12, 743–754. DOI: 10.1039/b921171c.
   Web of Science ®Google Scholar
• Thielbeer, F.; Donaldson, K.; Bradley, M. Zeta Potential Mediated Reaction Monitoring on Nano and Microparticles. Bioconjug. Chem. 2011, 22, 144–150. DOI: 10.1021/bc1005015.
   PubMed Web of Science ®Google Scholar
• van Deelen, T. W.; Mejia, C. H.; de Jong, K. P. Control of Metal-support Interactions in Heterogeneous Catalysts to Enhance Activity and Selectivity. Nature Catal. 2019, 2, 955–970.
   Web of Science ®Google Scholar
• Lokteva, E. S.; Golubina, E. V. Metal–support Interactions in the Design of Heterogeneous Catalysts for Redox Processes. Pure Appl. Chem. 2019, 91, 609–631. DOI: 10.1515/pac-2018-0715.
   Web of Science ®Google Scholar
• Ruppert, A. M., and Weckhuysen, B. M. Active phase-support interactions: metal–support Interactions. In Handbook of Heterogeneous Catalysis, 2nd Ed., Wiley-VCH, Weinheim, Ertl, G.; Knozinger, H.; Schuth, F.; Weitkamp, J. (Eds.), 2008; pp 1178–1188.
   Google Scholar
• Bingwa, N.; Patala, R.; Noh, J. H.; Ndolomingo, M. J.; Tetyana, S.; Bewana, S.; Meijboom, R. Synergistic Effects of Gold–palladium Nanoalloys and Reducible Supports on the Catalytic Reduction of 4-nitrophenol. Langmuir. 2017, 33, 7086–7095. DOI: 10.1021/acs.langmuir.7b00903.
   PubMed Web of Science ®Google Scholar
• Ordonez, S.; Daz, E.; Bueres, R. F.; Asedegbega-Nieto, E.; Sastre, H. Carbon Nanofibre-supported Palladium Catalysts as Model Hydrodechlorination Catalysts. J Catal. 2010, 272, 158–168. DOI: 10.1016/j.jcat.2010.03.001.
   Web of Science ®Google Scholar
• He, Z.; Dong, B.; Wang, W.; Yang, G.; Cao, Y.; Wang, H.; Yang, Y.; Wang, Q.; Peng, F.; Yu, H. Elucidating Interaction between Palladium and N-doped Carbon Nanotubes: Effect of Electronic Property on Activity for Nitrobenzene Hydrogenation. ACS Catal. 2019, 9, 2893–2901. DOI: 10.1021/acscatal.8b03965.
   Web of Science ®Google Scholar
• Fan, X.; Zhang, G.; Zhang, F. Multiple Roles of Graphene in Heterogeneous Catalysis. Chem. Soc. Rev. 2015, 44, 3023–3035. DOI: 10.1039/C5CS00094G.
   PubMed Web of Science ®Google Scholar
• Klaewkla, R.; Arend, M., and Hoelderich, W. F. A Review of Mass Transfer Controlling the Reaction Rate in Heterogeneous Catalytic Systems. Mass Transf. Adv. Aspects, Ch. 2011, 29, 667–684.
   Google Scholar
• Ertl, G.; Kno¨zinger, H., and Weitkamp, J. (Eds.). Handbook of Heterogeneous Catalysis (Vol. 2, pp. 427-440). 1997. Weinheim: VCH.
   Google Scholar
• Torres, G. C.; Jablonski, E. L.; Baronetti, G. T.; Castro, A. A.; De Miguel, S. R.; Scelza, O. A.; Blanco, M. D.; Pefia Jimenez, M. A.; Fierro, J. L. G. Effect of the Carbon Pre-treatment on the Properties and Performance for Nitrobenzene Hydrogenation of Pt/C Catalysts. Appl. Catal. A: General. 1997, 161, 213–226. DOI: 10.1016/S0926-860X(97)00071-9.
   Web of Science ®Google Scholar
• Li, Z.; Li, J.; Liu, J.; Zhao, Z.; Xia, C.; Li, F. Palladium Nanoparticles Supported on Nitrogen‐Functionalized Active Carbon: A Stable and Highly Efficient Catalyst for the Selective Hydrogenation of Nitroarenes. ChemCatChem. 2014, 6, 1333–1339.
   Web of Science ®Google Scholar
• Veerakumar, P.; Panneer Muthuselvam, I.; Hung, C. T.; Lin, K. C.; Chou, F. C.; Liu, S. B. Biomass-derived Activated Carbon Supported Fe3O4 Nanoparticles as Recyclable Catalysts for Reduction of Nitroarenes. ACS Sustainable Chem. Eng. 2016, 4, 6772–6782. DOI: 10.1021/acssuschemeng.6b01727.
   Web of Science ®Google Scholar
• Jyothi, T. M.; Rao, B. S.; Sugunan, S. Reduction of Nitroarenes with Isopropanol and Potassium Hydroxide over Metal Oxide Catalysts. Indian J. Chem. 2000, 39A, 1041–1043.
   Google Scholar
• Kulkarni, A. S.; Jayaram, R. V. Liquid Phase Catalytic Transfer Hydrogenation of Aromatic Nitro Compounds on La1−xSrxFeO3 Perovskites Prepared by Microwave Irradiation. J. Mol. Catal. A. 2004, 223, 107–110. DOI: 10.1016/j.molcata.2003.12.042.
   Web of Science ®Google Scholar
• Alonso, F.; Riente, P.; Reinoso, F. R.; Martez, J. R.; Escribano, A. S.; Yus, M. A Highly reusable Carbon-supported Platinum Catalyst for the Hydrogen-transfer Reduction of Ketones. ChemCatChem. 2009, 1, 75–77. DOI: 10.1002/cctc.200900045.
   Web of Science ®Google Scholar
• Subramanian, T.; Pitchumani, K. Selective Reduction of Nitroarenes by Using Zeolite-supported Copper Nanoparticles with 2-propanol as a Sustainable Reducing Agent. ChemCatChem. 2012, 4, 1917–1921. DOI: 10.1002/cctc.201200443.
   Web of Science ®Google Scholar
• Kadam, H. K.; Tilve, S. G. Advancement in Methodologies for Reduction of Nitroarenes. RSC Adv. 2015, 5, 83391–83407. DOI: 10.1039/C5RA10076C.
   Web of Science ®Google Scholar
• Huang, L.; Lv, Y.; Wu, S.; Liu, P.; Xiong, W.; Hao, F.; Luo, H. A. Activated Carbon Supported Bimetallic Catalysts with Combined Catalytic Effects for Aromatic Nitro Compounds Hydrogenation under Mild Conditions. Appl. Catal., A. 2019, 577, 76–85. DOI: 10.1016/j.apcata.2019.03.017.
   Web of Science ®Google Scholar
• Noschese, A.; Buonerba, A.; Canton, P.; Milione, S.; Capacchione, C.; Grassi, A. Highly Efficient and Selective Reduction of Nitroarenes into Anilines Catalysed by Gold Nanoparticles Incarcerated in a Nanoporous Polymer Matrix: Role of the Polymeric Support and Insight into the Reaction Mechanism. J. Catal. 2016, 340, 30–40.
   Web of Science ®Google Scholar
• Fang, H.; Wen, M.; Chen, H.; Wu, Q.; Li, W. Graphene Stabilized Ultra-small CuNi Nanocomposite with High Activity and Recyclability toward Catalysing the Reduction of Aromatic Nitro-compounds. Nanoscale. 2016, 8, 536–542. DOI: 10.1039/C5NR05016B.
   PubMed Web of Science ®Google Scholar
• Tang, Q.; Yuan, Z.; Jin, S.; Yao, K.; Yang, H.; Chi, Q.; Liu, B. Biomass-derived Carbon-supported Ni Catalyst: An Effective Heterogeneous Non-noble Metal Catalyst for the Hydrogenation of Nitro Compounds. React. Chem. Eng. 2020, 5, 58–65. DOI: 10.1039/C9RE00366E.
   Web of Science ®Google Scholar
• Duan, Y.; Song, T.; Dong, X.; Yang, Y. Enhanced Catalytic Performance of Cobalt Nanoparticles Coated with a N, P-codoped Carbon Shell Derived from Biomass for Transfer Hydrogenation of Functionalized Nitroarenes. Green Chem. 2018, 20, 2821–2828. DOI: 10.1039/C8GC00619A.
   Web of Science ®Google Scholar
• Zhu, Q.; Sun, X.; Zhao, H.; Xu, D.; Dong, Z. The Selective Transfer Hydrogenation and N-formylation of Nitroarenes by Facilely-prepared N, S Co-doped Carbon Encapsulated Cobalt Nanoparticles Catalyst. Ind. Eng. Chem. Res. 2020, 59, 5615–5623. DOI 10.1021/acs.iecr.9b06366.
   Web of Science ®Google Scholar
• Iijima, S. Helical Microtubules of Graphitic Carbon. Nature. 1991, 354, 56–58. DOI: 10.1038/354056a0.
   Web of Science ®Google Scholar
• John, J.; Gravel, E.; Namboothiri, I. N.; Doris, E. Advances in Carbon Nanotube-noble Metal Catalysed Organic Transformations. Nanotechnol. Rev. 2012, 1, 515–539. DOI: 10.1515/ntrev-2012-0025.
   Web of Science ®Google Scholar
• Chen, P.; Yang, F.; Kostka, A.; Xia, W. Interaction of Cobalt Nanoparticles with Oxygen-and Nitrogen-functionalized Carbon Nanotubes and Impact on Nitrobenzene Hydrogenation Catalysis. ACS Catal. 2014, 4, 1478–1486. DOI: 10.1021/cs500173t.
   Web of Science ®Google Scholar
• Dong, B.; Li, Y.; Ning, X.; Wang, H.; Yu, H.; Peng, F. Trace Iron Impurities Deactivate Palladium Supported on Nitrogen-doped Carbon Nanotubes for Nitrobenzene Hydrogenation. Appl. Catal. A: General. 2017, 545, 54–63. DOI: 10.1016/j.apcata.2017.07.035.
   Web of Science ®Google Scholar
• Carturan, G.; Facchin, G.; Cocco, G.; Navazio, G.; Gubitosa, G. Hydrogenation of Nitrocompounds with Supported Palladium Catalysts: Influence of Metal Dispersion and Nitrocompound Nature. J. Catal. 1983, 82, 56–65. DOI: 10.1016/0021-9517(83)90117-3.
   Web of Science ®Google Scholar
• Chinthaginjala, J. K.; Villa, A.; Su, D. S.; Mojet, B. L.; Lefferts, L. Nitrite Reduction over Pd Supported CNFs: Metal Particle Size Effect on Selectivity. Catal. Today. 2012, 183, 119–123. DOI: 10.1016/j.cattod.2011.11.003.
   Web of Science ®Google Scholar
• Semagina, N.; Renken, A.; Kiwi-Minsker, L. Palladium Nanoparticle Size Effect in 1-hexyne Selective Hydrogenation. J. Phys. Chem. C. 2007, 111, 13933–13937. DOI: 10.1021/jp073944k.
   Web of Science ®Google Scholar
• Neri, G.; Musolino, M. G.; Milone, C.; Pietropaolo, D.; Galvagno, S. Particle Size Effect in the Catalytic Hydrogenation of 2, 4-dinitrotoluene over Pd/C Catalysts. Appl. Catal. A: General. 2001, 208, 307–316. DOI: 10.1016/S0926-860X(00)00717-1.
   Web of Science ®Google Scholar
• Semagina, N.; Renken, A.; Laub, D.; Kiwi-Minsker, L. Synthesis of Monodispersed Palladium Nanoparticles to Study Structure Sensitivity of Solvent-free Selective Hydrogenation of 2-methyl-3-butyn-2-ol. J. Catal. 2007, 246, 308–314.
   Web of Science ®Google Scholar
• Jawale, D. V.; Gravel, E.; Boudet, C.; Shah, N.; Geertsen, V.; Li, H.; Namboothiri, I. N. N.; Doris, E. Selective Conversion of Nitroarenes Using a Carbon Nanotube–ruthenium Nanohybrid. Chem. Comm. 2015, 51, 1739–1742. DOI: 10.1039/C4CC09192B.
   PubMed Web of Science ®Google Scholar
• Uozumi, Y.; Yamada, Y. M.; Ohno, A. Hydrogenation of Nitroarenes Using a Carbon Nanotube–Ruthenium Nanohybrid. Synfacts. 2015, 11, 0442–0442−.
   Google Scholar
• Tomkins, P.; Gebauer-Henke, E.; Leitner, W.; Müller, T. E. Concurrent Hydrogenation of Aromatic and Nitro Groups over Carbon-supported Ruthenium Catalysts. ACS Catal. 2015, 5, 203–209. DOI: 10.1021/cs501122h.
   Web of Science ®Google Scholar
• Gu, X.; Qi, W.; Xu, X.; Sun, Z.; Zhang, L.; Liu, W.; Pan, X.; Su, D. Covalently Functionalized Carbon Nanotube Supported Pd Nanoparticles for Catalytic Reduction of 4-nitrophenol. Nanoscale. 2014, 6, 6609–6616. DOI: 10.1039/C4NR00826J.
   PubMed Web of Science ®Google Scholar
• Dreyer, D. R.; Park, S.; Bielawski, C. W.; Ruoff, R. S. The Chemistry of Graphene Oxide. Chem. Soc. Rev. 2010, 39, 228–240. DOI: 10.1039/B917103G.
   PubMed Web of Science ®Google Scholar
• Wei, Z.; Pan, R.; Hou, Y.; Yang, Y.; Liu, Y. Graphene-supported Pd Catalyst for Highly Selective Hydrogenation of Resorcinol to 1, 3-cyclohexanedione through Giant π-conjugate Interactions. Sci. Rep. 2015, 5, 15664–15673. DOI: 10.1038/srep15664.
   PubMed Web of Science ®Google Scholar
• Su, Q.; Pang, S.; Alijani, V.; Li, C.; Feng, X.; Müllen, K. Composites of Graphene with Large Aromatic Molecules. Adv. Mater. 2009, 21, 3191–3195. DOI: 10.1002/adma.200803808.
   Web of Science ®Google Scholar
• Xiao, F.; Pignatello, J. J. π–π Interactions between (Hetero) Aromatic Amine Cations and the Graphitic Surfaces of Pyrogenic Carbonaceous Materials. Environ. Sci. Technol. 2015, 49, 906–914. DOI: 10.1021/es5043029.
   PubMed Web of Science ®Google Scholar
• Balamurugan, K.; Subramanian, V. Adsorption of Chlorobenzene onto (5,5) Armchair Single-Walled Carbon Nanotube and Graphene Sheet: Toxicity versus Adsorption Strength. J. Phys. Chem. C. 2013, 117, 21217–21227. DOI: 10.1021/jp403646h.
   Web of Science ®Google Scholar
• Feng, Y. S.; Ma, J. J.; Kang, Y. M.; Xu, H. J. PdCu Nanoparticles Supported on Graphene: An Efficient and Recyclable Catalyst for Reduction of Nitroarenes. Tetrahedron. 2014, 70, 6100–6105. DOI: 10.1016/j.tet.2014.04.034.
   Web of Science ®Google Scholar
• Jagadeesh, R. V.; Natte, K.; Junge, H.; Beller, M. Nitrogen-doped Graphene-activated Iron-oxide-based Nanocatalysts for Selective Transfer Hydrogenation of Nitroarenes. ACS Catal. 2015, 5, 1526–1529. DOI: 10.1021/cs501916p.
   Web of Science ®Google Scholar
• Dideikin, A. T.; Vul, A. Y. Graphene Oxide and Derivatives: The Place in Graphene Family. Front. Phys. 2019, 6, 149. DOI: 10.3389/fphy.2018.00149.
   Web of Science ®Google Scholar
• Xiao, D.; Sun, W.; Dai, H.; Zhang, Y.; Qin, X.; Li, L.; Wei, Z.; Chen, X. Influence of Charge States on the π–π Interactions of Aromatic Side Chains with Surface of Graphene Sheet and Single-walled Carbon Nanotubes in Bioelectrodes. J. Phys. Chem. C. 2014, 118, 20694–20701. DOI: 10.1021/jp506336c.
   Web of Science ®Google Scholar
• Kandathil, V.; Kulkarni, B.; Siddiqa, A.; Kempasiddaiah, M.; Sasidhar, B. S.; Patil, S. A.; Patil, S. A. Immobilized N-Heterocyclic Carbene-Palladium (II) Complex on Graphene Oxide as Efficient and Recyclable Catalyst for Suzuki–Miyaura Cross-Coupling and Reduction of Nitroarenes. Cataly. Lett. 2020, 150, 384–403. DOI: 10.1007/s10562-019-03083-0.
   Web of Science ®Google Scholar
• Bilgicli, H. G.; Burhan, H.; Diler, F.; Cellat, K.; Kuyuldar, E.; Zengin, M.; Sen, F. Composites of Palladium Nanoparticles and Graphene Oxide as a Highly Active and Reusable Catalyst for the Hydrogenation of Nitroarenes. Microporous Mesoporous Mater. 2020, 296, 110014. DOI: 10.1016/j.micromeso.2020.110014.
   Web of Science ®Google Scholar
• Smith, A. T.; LaChance, A. M.; Zeng, S.; Liu, B.; Sun, L. Synthesis, Properties, and Applications of Graphene Oxide/reduced Graphene Oxide and Their Nanocomposites. Nanomater Sci. 2019, 1, 31–47.
   Google Scholar
• Tarcan, R.; Todor-Boer, O.; Petrovai, I.; Leordean, C.; Astilean, S.; Botiz, I. Reduced Graphene Oxide Today. J. Mater. Chem. C. 2020, 8, 1198–1224. DOI: 10.1039/C9TC04916A.
   Web of Science ®Google Scholar
• Kumar, R.; Ansari, M. O.; Barakat, M. A., and Rashid, J. Graphene/metal Oxide–based Nanocomposite as Photocatalyst for Degradation of Water Pollutants. Graphene-Based Nanotechnol. Energy Environ. 2019, 221–240. DOI:10.1016/B978-0-12-815811-1.00013-2.
   Google Scholar
• Nie, R.; Wang, J.; Wang, L.; Qin, Y.; Chen, P.; Hou, Z. Platinum Supported on Reduced Graphene Oxide as a Catalyst for Hydrogenation of Nitroarenes. Carbon. 2012, 50, 586–596. DOI: 10.1016/j.carbon.2011.09.017.
   Web of Science ®Google Scholar
• El-Hout, S. I.; El-Sheikh, S. M.; Hassan, H. M.; Harraz, F. A.; Ibrahim, I. A.; El-Sharkawy, E. A. A Green Chemical Route for Synthesis of Graphene Supported Palladium Nanoparticles: A Highly Active and Recyclable Catalyst for Reduction of Nitrobenzene. Appl. Catal., A. 2015, 503, 176–185. DOI: 10.1016/j.apcata.2015.06.036.
   Web of Science ®Google Scholar
• Metin, O.; Can, H.; Şendil, K.; Gültekin, M. S. Monodisperse Ag/Pd Core/shell Nanoparticles Assembled on Reduced Graphene Oxide as Highly Efficient Catalysts for the Transfer Hydrogenation of Nitroarenes. J. Colloid Interface Sci. 2017, 498, 378–386. DOI: 10.1016/j.jcis.2017.03.066.
   PubMed Web of Science ®Google Scholar
• Metin, O.; Mendoza-Garcia, A.; Dalmızrak, D.; Gültekin, M. S.; Sun, S. FePd Alloy Nanoparticles Assembled on Reduced Graphene Oxide as a Catalyst for Selective Transfer Hydrogenation of Nitroarenes to Anilines Using Ammonia Borane as a Hydrogen Source. Catal. Sci. Technol. 2016, 6, 6137–6143. DOI: 10.1039/C6CY00118A.
   Web of Science ®Google Scholar
• Nasrollahzadeh, M.; Sajadi, S. M.; Rostami-Vartooni, A.; Alizadeh, M.; Bagherzadeh, M. Green Synthesis of the Pd Nanoparticles Supported on Reduced Graphene Oxide Using Barberry Fruit Extract and Its Application as a Recyclable and Heterogeneous Catalyst for the Reduction of Nitroarenes. J. Colloid Interface Sci. 2016, 466, 360–368. DOI: 10.1016/j.jcis.2015.12.036.
   PubMed Web of Science ®Google Scholar
• Liu, X.; Wang, C.; Cheng, S.; Shang, N.; Gao, S.; Feng, C.; Wang, C.; Qiao, Y.; Wang, Z. Agpd Nanoparticles Supported on Reduced Graphene Oxide: A High Catalytic Activity Catalyst for the Transfer Hydrogenation of Nitroarenes. Catal. Commun. 2018, 108, 103–107. DOI: 10.1016/j.catcom.2018.02.001.
   Web of Science ®Google Scholar
• Fan, G. Y.; Huang, W. J. Synthesis of Ruthenium/reduced Graphene Oxide Composites and Application for the Selective Hydrogenation of Halonitroaromatics. Chin. Chem. Lett. 2014, 25, 359–363. DOI: 10.1016/j.cclet.2013.11.044.
   Web of Science ®Google Scholar
• Dong, W.; Cheng, S.; Feng, C.; Shang, N.; Gao, S.; Wang, C. Fabrication of Highly Dispersed Pd Nanoparticles Supported on Reduced Graphene Oxide for Catalytic Reduction of 4-nitrophenol. Catal. Commun. 2017, 90, 70–74. DOI: 10.1016/j.catcom.2016.11.021.
   Web of Science ®Google Scholar
• Goswami, A.; Kadam, R. G.; Tuček, J.; Sofer, Z.; Bouša, D.; Varma, R. S.; Gawande, M. B.; Zbořil, R. Fe (0)-embedded Thermally Reduced Graphene Oxide as Efficient Nanocatalyst for Reduction of Nitro Compounds to Amines. Chem. Eng. J. 2020, 382, 122469. DOI: 10.1016/j.cej.2019.122469.
   Web of Science ®Google Scholar
• Liu, X.; Zhao, X.; Zhou, M.; Cao, Y.; Wu, H.; Zhu, J. Highly Stable and Active Palladium Nanoparticles Supported on a Mesoporous UiO66@ Reduced Graphene Oxide Complex for Practical Catalytic Applications. Eur. J. Inorg. Chem. 2016, 2016, 3338–3343. DOI: 10.1002/ejic.201600367.
   Google Scholar
• Antolini, E. Carbon Supports for Low-temperature Fuel Cell Catalysts. Appl. Catal., B. 2009, 88, 1–24. DOI: 10.1016/j.apcatb.2008.09.030.
   Web of Science ®Google Scholar
• Feng, R.; Li, M.; Liu, J. Synthesis of Core–shell Au@ Pt Nanoparticles Supported on Vulcan XC-72 Carbon and Their Electrocatalytic Activities for Methanol Oxidation. Colloids Surf., A. 2012, 406, 6–12. DOI: 10.1016/j.colsurfa.2012.04.030.
   Google Scholar
• Şener, T.; Kayhan, E.; Sevim, M.; Metin, I. Monodisperse CoFe2O4 Nanoparticles Supported on Vulcan XC-72: High Performance Electrode Materials for Lithium-air and Lithium-ion Batteries. J. Power Sources. 2015, 288, 36–41. DOI: 10.1016/j.jpowsour.2015.04.120.
   Web of Science ®Google Scholar
• Gharibi, H.; Kakaei, K.; Zhiani, M. Platinum Nanoparticles Supported by a Vulcan XC-72 and PANI Doped with Trifluoromethane Sulfonic Acid Substrate as a New Electrocatalyst for Direct Methanol Fuel Cells. J. Phys. Chem. C. 2010, 114, 5233–5240. DOI: 10.1021/jp9119414.
   Web of Science ®Google Scholar
• Gao, S.; Feng, T.; Wu, Q.; Feng, C.; Shang, N.; Wang, C. Immobilizing AgPd Alloy on Vulcan XC-72 Carbon: A Novel Catalyst for Highly Efficient Hydrogen Generation from Formaldehyde Aqueous Solution. RSC Adv. 2016, 6, 105638–105643. DOI: 10.1039/C6RA22761A.
   Web of Science ®Google Scholar
• Wang, Z. L.; Yan, J. M.; Wang, H. L.; Ping, Y.; Jiang, Q. Pd/C Synthesized with Citric Acid: An Efficient Catalyst for Hydrogen Generation from Formic Acid/sodium Formate. Sci. Rep. 2012, 2, 203–598. DOI: 10.1038/srep00598.
   Web of Science ®Google Scholar
• Westerhaus, F. A.; Jagadeesh, R. V.; Wienhöfer, G.; Pohl, M. M.; Radnik, J.; Surkus, A. E.; Rabeah, J.; Junge, K.; Nielsen, M.; Brückner, A, et al. Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes. Nature Chem. 2013, 5, 537–543. DOI: 10.1038/nchem.1645.
   PubMed Web of Science ®Google Scholar
• Liu, W.; Zhang, L.; Yan, W.; Liu, X.; Yang, X.; Miao, S.; Wang, W.; Wang, A.; Zhang, T. Single-atom Dispersed Co–N–C Catalyst: Structure Identification and Performance for Hydrogenative Coupling of Nitroarenes. Chem. Sci. 2016, 7, 5758–5764. DOI: 10.1039/C6SC02105K.
   PubMed Web of Science ®Google Scholar
• Jagadeesh, R. V.; Surkus, A. E.; Junge, H.; Pohl, M. M.; Radnik, J.; Rabeah, J.; Huan, H.; Schunemann, V.; Bruckner, A.; Beller, M. Nanoscale Fe2O3-based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines. Science. 2013, 342, 1073–1076.
   PubMed Web of Science ®Google Scholar
• Chen, J.; Yao, Y.; Zhao, J.; Zhao, Y.; Zheng, Y.; Li, M.; Yang, Q. A Highly Active Non-precious Metal Catalyst Based on Fe–N–C@ CNTs for Nitroarene Reduction. RSC Adv. 2016, 6, 96203–96209.
   Web of Science ®Google Scholar
• Zhang, L.; Liu, X.; Zhou, X.; Gao, S.; Shang, N.; Feng, C.; Wang, C. Ultrafine Pd Nanoparticles Anchored on Nitrogen-doping Carbon for Boosting Catalytic Transfer Hydrogenation of Nitroarenes. ACS Omega. 2018, 3, 10843–10850. DOI: 10.1021/acsomega.8b01141.
   PubMed Web of Science ®Google Scholar
• Liu, L.; Concepcion, P.; Corma, A. Non-noble Metal Catalysts for Hydrogenation: A Facile Method for Preparing Co Nanoparticles Covered with Thin Layered Carbon. J. Catal. 2016, 340, 1–9. DOI: 10.1016/j.jcat.2016.04.006.
   Web of Science ®Google Scholar
• Liu, L.; Gao, F.; Concepción, P.; Corma, A. A New Strategy to Transform Mono and Bimetallic Non-noble Metal Nanoparticles into Highly Active and Chemoselective Hydrogenation Catalysts. J. Catal. 2017, 350, 218–225. DOI: 10.1016/j.jcat.2017.03.014.
   Web of Science ®Google Scholar
• Zhang, L.; Zhou, M.; Wang, A.; Zhang, T. Selective Hydrogenation over Supported Metal Catalysts: From Nanoparticles to Single Atoms. Chem. Rev. 2020, 120, 683–733. DOI: 10.1021/acs.chemrev.9b00230.
   PubMed Web of Science ®Google Scholar
• Ruiz Puigdollers, A.; Schlexer, P.; Tosoni, S.; Pacchioni, G. Increasing Oxide Reducibility: The Role of Metal/oxide Interfaces in the Formation of Oxygen Vacancies. ACS Catal. 2017, 7, 6493–6513. DOI: 10.1021/acscatal.7b01913.
   Web of Science ®Google Scholar
• Jupille, J.; Thornton, G. In Defects at Oxide Surfaces; Heidelberg: Germany,Springer:, 2015.
   Google Scholar
• Gawande, M. B.; Pandey, R. K.; Jayaram, R. V. Role of Mixed Metal Oxides in Catalysis Science−versatile Applications in Organic Synthesis. Catal. Sci. Technol. 2012, 2, 1113–1125. DOI: 10.1039/c2cy00490a.
   Web of Science ®Google Scholar
• Tauster, S. J.; Fung, S. C.; Baker, R. T. K.; Horsley, J. A. Strong Interactions in Supported-metal Catalysts. Science. 1981, 211, 1121–1125. DOI: 10.1126/science.211.4487.1121.
   PubMed Web of Science ®Google Scholar
• Bagheri, S.; Muhd Julkapli, N.; Bee Abd Hamid, S. Titanium Dioxide as a Catalyst Support in Heterogeneous Catalysis. Sci. World J. 2014, 2014, 1–21. DOI: 10.1155/2014/727496).
   Google Scholar
• Kim, T. S.; Stiehl, J. D.; Reeves, C. T.; Meyer, R. J.; Mullins, C. B. Cryogenic CO Oxidation on TiO2-supported Gold Nanoclusters Pre-covered with Atomic Oxygen. J. Am. Chem. Soc. 2003, 125, 2018–2019. DOI: 10.1021/ja028719p.
   PubMed Web of Science ®Google Scholar
• Oi, L. E.; Choo, M. Y.; Lee, H. V.; Ong, H. C.; Hamid, S. B. A.; Juan, J. C. Recent Advances of Titanium Dioxide (Tio2) for Green Organic Synthesis. RSC Adv. 2016, 6, 108741–108754. DOI: 10.1039/C6RA22894A.
   Web of Science ®Google Scholar
• Manyar, H. G.; Paun, C.; Pilus, R.; Rooney, D. W.; Thompson, J. M.; Hardacre, C. Highly Selective and Efficient Hydrogenation of Carboxylic Acids to Alcohols Using Titania Supported Pt Catalysts. Chem. Commun. 2010, 46, 6279–6281. DOI: 10.1039/c0cc01365j.
   PubMed Web of Science ®Google Scholar
• Yan, W.; Mahurin, S. M.; Pan, Z.; Overbury, S. H.; Dai, S. Ultra-stable Au Nanocatalyst Supported on Surface-modified TiO2 Nanocrystals. J. Am. Chem. Soc. 2005, 127, 10480–10481. DOI: 10.1021/ja053191k.
   PubMed Web of Science ®Google Scholar
• Manr´ıquez, M. E. ;.; Opez, T. L.; Omez, R. G.; Navarrete, J. Preparation of TiO2–ZrO2 Mixed Oxides with Controlled Acid–basic Properties. J. Mol. Catal. A Chem. 2004, 220, 229–237. DOI: 10.1016/j.molcata.2004.06.003.
   Web of Science ®Google Scholar
• Makosch, M.; Lin, W. I.; Bumbálek, V.; Sá, J.; Medlin, J. W.; Hungerbühler, K.; van Bokhoven, J. A. Organic Thiol Modified Pt/TiO2 Catalysts to Control Chemoselective Hydrogenation of Substituted Nitroarenes. ACS Catal. 2012, 2, 2079–2081. DOI: 10.1021/cs300378p.
   Web of Science ®Google Scholar
• Bartholomew, C. H. Mechanisms of Catalyst Deactivation. Appl. Catal., A. 2001, 212, 17–60. DOI 10.1016/S0926-860X(00)00843-7.
   Web of Science ®Google Scholar
• Chen, P.; Khetan, A.; Yang, F.; Migunov, V.; Weide, P.; Stürmer, S. P.; Guo, P.; Kahler, K.; Xia, W.; Mayer, J, et al. Experimental and Theoretical Understanding of Nitrogen-doping-induced Strong Metal–support Interactions in Pd/TiO2 Catalysts for Nitrobenzene Hydrogenation. ACS Catal. 2017, 7, 1197–1206.
   Web of Science ®Google Scholar
• Raj, K. J. A.; Prakash, M. G.; Mahalakshmy, R.; Elangovan, T.; Viswanathan, B. Liquid Phase Hydrogenation of Nitrobenzene over Nickel Supported on Titania. Chin. J. Catal. 2012, 33, 1299–1305. DOI: 10.1016/S1872-2067(11)60398-7.
   Web of Science ®Google Scholar
• Shukla, A.; Singha, R. K.; Sasaki, T.; Adak, S.; Bhandari, S.; Prasad, V. V. D. N.; Bordoloi, A.; Bal, R. Room Temperature Selective Reduction of Nitroarenes to Azoxy Compounds over Ni-TiO2 Catalyst. Mol. Catal. 2020, 490, 110943–110953.
   Google Scholar
• Qu, R.; Macino, M.; Iqbal, S.; Gao, X.; He, Q.; Hutchings, G. J.; Sankar, M. Supported Bimetallic AuPd Nanoparticles as a Catalyst for the Selective Hydrogenation of Nitroarenes. Nanomaterials. 2018, 8, 690–700. DOI: 10.3390/nano8090690.
   Web of Science ®Google Scholar
• Zou, L.; Cui, Y.; Dai, W. Highly Efficient Au/TiO2 Catalyst for One‐pot Conversion of Nitrobenzene to p‐Aminophenol in Water Media. Chin. J. Chem. 2014, 32, 257–262. DOI: 10.1002/cjoc.201300875.
   Web of Science ®Google Scholar
• Kuhaudomlap, S.; Mekasuwandumrong, O.; Praserthdam, P.; Fujita, S. I.; Arai, M.; Panpranot, J. The H2-Treated TiO2 Supported Pt Catalysts Prepared by Strong Electrostatic Adsorption for Liquid-Phase Selective Hydrogenation. Catalysts. 2018, 8, 87–98. DOI: 10.3390/catal8020087.
   Web of Science ®Google Scholar
• Fujita, S. I.; Yoshida, H.; Asai, K.; Meng, X.; Arai, M. Selective Hydrogenation of Nitrostyrene to Aminostyrene over Pt/TiO2 Catalysts: Effects of Pressurized Carbon Dioxide and Catalyst Preparation Conditions. J. Supercrit. Fluids. 2011, 60, 106–112. DOI: 10.1016/j.supflu.2011.02.016.
   Web of Science ®Google Scholar
• Yoshida, H.; Igarashi, N.; Fujita, S. I.; Panpranot, J.; Arai, M. Influence of Crystallite Size of TiO2 Supports on the Activity of Dispersed Pt Catalysts in Liquid-phase Selective Hydrogenation of 3-nitrostyrene, Nitrobenzene and Styrene. Catal. Lett. 2014, 145, 606–611. DOI: 10.1007/s10562-014-1404-4.
   Web of Science ®Google Scholar
• Pisduangdaw, S.; Mekasuwandumrong, O.; Yoshida, H.; Fujita, S. I.; Arai, M.; Panpranot, J. Flame-made Pt/TiO2 Catalysts for the Liquid-phase Selective Hydrogenation of 3-nitrostyrene. Appl. Catal. A. 2015, 490, 193–200. DOI: 10.1016/j.apcata.2014.10.002.
   Web of Science ®Google Scholar
• Varkolu, M.; Velpula, V.; Pochamoni, R.; Muppala, A. R.; Burri, D. R.; Kamaraju, S. R. R. Nitrobenzene Hydrogenation over Ni/TiO2 Catalyst in Vapour Phase at Atmospheric Pressure: Influence of Preparation Method. Appl. Petrochem. Res. 2016, 6, 15–23. DOI: 10.1007/s13203-015-0115-0.
   Web of Science ®Google Scholar
• González-Vera, D.; Bustamante, T. M.; de León, J. D.; Dinamarca, R.; Morales, R.; Osorio-Vargas, P. A.; Torres, C. C., and Campos, C. H. Chemoselective Nitroarene Hydrogenation over Ni-Pd Alloy Supported on TiO2 Prepared from Ilmenite-type PdxNi1−xTiO3. Mater. Today Commun. 2020, 24, 101091–101112. DOI: 10.1016/j.mtcomm.2020.101091.
   Web of Science ®Google Scholar
• Corma, A.; Serna, P.; Concepción, P.; Calvino, J. J. Transforming Nonselective into Chemoselective Metal Catalysts for the Hydrogenation of Substituted Nitroaromatics. J. Am. Chem. Soc. 2008, 130, 8748–8753. DOI: 10.1021/ja800959g.
   PubMed Web of Science ®Google Scholar
• Sharma, R. K.; Dutta, S.; Sharma, S.; Zboril, R.; Varma, R. S.; Gawande, M. B. Fe3O4 (Iron Oxide)-supported Nanocatalysts: Synthesis, Characterization and Applications in Coupling Reactions. Green Chem. 2016, 18, 3184–3209. DOI: 10.1039/C6GC00864J.
   Web of Science ®Google Scholar
• Shifrina, Z. B.; Bronstein, L. M. Magnetically Recoverable Catalysts: Beyond Magnetic Separation. Front. Chem. 2018, 6, 298. DOI: 10.3389/fchem.2018.00298.
   PubMed Web of Science ®Google Scholar
• Wu, W.; He, Q.; Jiang, C. Magnetic Iron Oxide Nanoparticles: Synthesis and Surface Functionalization Strategies. Nanoscale Res. Lett. 2008, 3, 397. DOI: 10.1007/s11671-008-9174-9.
   PubMed Web of Science ®Google Scholar
• Niu, H.; Lu, J.; Song, J.; Pan, L.; Zhang, X.; Wang, L.; Zou, J. J. Iron Oxide as a Catalyst for Nitroarene Hydrogenation: Important Role of Oxygen Vacancies. Ind. Eng. Chem. Res. 2016, 55, 8527–8533. DOI: 10.1021/acs.iecr.6b00984.
   Web of Science ®Google Scholar
• Ma, Y.; Zhang, L.; Shi, W.; Niu, Y.; Zhang, B.; Su, D. Facile-fabricated Iron Oxide Nanorods as a Catalyst for Hydrogenation of Nitrobenzene. Chin. J. Catal. 2019, 30, 183–186.
   Google Scholar
• Lin, F. H.; Doong, R. A. Bifunctional Au−Fe3O4 Heterostructures for Magnetically Recyclable Catalysis of Nitrophenol Reduction. J. Phys. Chem. C. 2011, 115, 6591–6598. DOI: 10.1021/jp110956k.
   Web of Science ®Google Scholar
• Jing, P.; Gan, T.; Qi, H.; Zheng, B.; Chu, X.; Yu, G.; Yan, W.; Zou, Y.; Zhang, W.; Liu, G. Synergism of Pt Nanoparticles and Iron Oxide Support for Chemoselective Hydrogenation of Nitroarenes under Mild Conditions. Chin. J. Catal. 2019, 40, 214–222. DOI 10.1016/S1872-2067(19)63276-6.
   Web of Science ®Google Scholar
• Wei, H.; Liu, X.; Wang, A.; Zhang, L.; Qiao, B.; Yang, X.; Huang, Y.; Miao, S.; Liu, J.; Zhang, T. FeOx-supported Platinum Single-atom and Pseudo-single-atom Catalysts for Chemoselective Hydrogenation of Functionalized Nitroarenes. Nat. Commun. 2014, 5, 5634. DOI: 10.1038/ncomms6634.
   PubMed Web of Science ®Google Scholar
• Byun, S.; Song, Y.; Kim, B. M. Heterogenized Bimetallic Pd–Pt–Fe3O4 Nanoflakes as Extremely Robust, Magnetically Recyclable Catalysts for Chemoselective Nitroarene Reduction. ACS Appl. Mater. Interfaces. 2016, 8, 14637–14647. DOI: 10.1021/acsami.6b05229.
   PubMed Web of Science ®Google Scholar
• Easterday, R.; Sanchez-Felix, O.; Losovyj, Y.; Pink, M.; Stein, B. D.; Morgan, D. G.; Rakitin, M.; Yu, V.; Sulman, D. M. G.; Mahmoud, W. E, et al. Design of Ruthenium/iron Oxide Nanoparticle Mixtures for Hydrogenation of Nitrobenzene. Catal. Sci. Technol. 2015, 5, 1902–1910. DOI: 10.1039/C4CY01277A.
   Web of Science ®Google Scholar
• Pélisson, C. H.; Denicourt‐Nowicki, A.; Meriadec, C.; Greneche, J. M.; Roucoux, A. Magnetically Recoverable Palladium (0) Nanocomposite Catalyst for Hydrogenation Reactions in Water. ChemCatChem. 2015, 7, 309–315. DOI: 10.1002/cctc.201402761.
   Web of Science ®Google Scholar
• Biglione, C.; Cappelletti, A. L.; Strumia, M. C.; Martín, S. E.; Uberman, P. M. Magnetic Pd Nanocatalyst Fe3O4@Pd for C–C Bond Formation and Hydrogenation Reactions. J. Nanopart. Res. 2018, 20, 127–142. DOI: 10.1007/s11051-018-4233-3.
   Web of Science ®Google Scholar
• Shokouhimehr, M. Magnetically Separable and Sustainable Nanostructured Catalysts for Heterogeneous Reduction of Nitroaromatics. Catalysts. 2015, 5, 534–560. DOI: 10.3390/catal5020534.
   Web of Science ®Google Scholar
• Shukla, A.; Singha, R. K.; Sasaki, T.; Prasad, V. V.; Bal, R. Synthesis of Highly Active Pd Nanoparticles Supported Iron Oxide Catalyst for Selective Hydrogenation and Cross‐Coupling Reactions in Aqueous Medium. ChemistrySelect. 2019, 4, 5019–5032. DOI: 10.1002/slct.201900358.
   Web of Science ®Google Scholar
• Gawande, M. B.; Rathi, A. K.; Branco, P. S.; Nogueira, I. D.; Velhinho, A.; Shrikhande, J. J.; Indulkar, U. U.; Jayaram, R. V.; Ghumman, C. A. A.; Bundaleski, N, et al. Regio‐and Chemoselective Reduction of Nitroarenes and Carbonyl Compounds over Recyclable Magnetic Ferrite-Nickel Nanoparticles (Fe3o4- Ni) by Using Glycerol as a Hydrogen Source. Chem. - Eur. J. 2012, 18, 12628–12632. DOI: 10.1002/chem.201202380.
   PubMed Web of Science ®Google Scholar
• Jiang, T.; Du, S.; Jafari, T.; Zhong, W.; Sun, Y.; Song, W.; Luo, Z.; Hines, W. A.; Suib, S. L. Synthesis of Mesoporous γ-Fe2O3 Supported Palladium Nanoparticles and Investigation of Their Roles as Magnetically Recyclable Catalysts for Nitrobenzene Hydrogenation. Appl. Catal., A. 2015, 502, 105–113. DOI: 10.1016/j.apcata.2015.05.013.
   Web of Science ®Google Scholar
• Zhang, R.; Liu, J.; Li, F.; Wu, S.; Xia, C.; Sun, W. Magnetically Separable and Versatile Pd/Fe3O4 Catalyst for Efficient Suzuki Cross‐Coupling Reaction and Selective Hydrogenation of Nitroarenes. Chin. J. Chem. 2011, 29, 525–530.
   Web of Science ®Google Scholar
• Zeynizadeh, B.; Mohammadzadeh, I.; Shokri, Z.; Hosseini, S. A. Synthesis and Characterization of NiFe2O4@Cu Nanoparticles as a Magnetically Recoverable Catalyst for Reduction of Nitroarenes to Arylamines with NaBH4. J. Colloid Interface Sci. 2017, 500, 285–293. DOI: 10.1016/j.jcis.2017.03.030.
   PubMed Web of Science ®Google Scholar
• Patra, A. K.; Vo, N. T.; Kim, D. Highly Robust Magnetically Recoverable Ag/Fe2O3 Nanocatalyst for Chemoselective Hydrogenation of Nitroarenes in Water. Appl. Catal., A. 2017, 538, 148–156. DOI 10.1016/j.apcata.2017.03.007.
   Web of Science ®Google Scholar
• Naaz, F.; Farooq, U., and Ahmad, T. Ceria as an Efficient Nanocatalyst for Organic Transformations. In I. Sinha, & M. Shukla (Eds.), Nanocatalysts. IntechOpen. 2019. DOI: 10.5772/intechopen.82688.
   Google Scholar
• Rodriguez, J. A.; Grinter, D. C.; Liu, Z.; Palomino, R. M.; Senanayake, S. D. Ceria-based Model Catalysts: Fundamental Studies on the Importance of the Metal–ceria Interface in CO Oxidation, the Water–gas Shift, CO2 Hydrogenation, and Methane and Alcohol Reforming. Chem. Soc. Rev. 2017, 46, 1824–1841. DOI: 10.1039/C6CS00863A.
   PubMed Web of Science ®Google Scholar
• Montini, T.; Melchionna, M.; Monai, M.; Fornasiero, P. Fundamentals and Catalytic Applications of CeO2-based Materials. Chem. Rev. 2016, 116, 5987–6041. DOI: 10.1021/acs.chemrev.5b00603.
   PubMed Web of Science ®Google Scholar
• Segura, Y.; Lopez, N; Perez-Ramirez, J. Origin of the Superior Hydrogenation Selectivity of Gold Nanoparticles in Alkyne + Alkene Mixtures: Triple- versus Double-Bond Activation. J. Catal. 2007, 247, 383–386. DOI: 10.1016/j.jcat.2007.02.019.
   Web of Science ®Google Scholar
• Azizi, Y.; Petit, C.; Pitchon, V. Formation of Polymer-Grade Ethylene by Selective Hydrogenation of Acetylene over Au/CeO2. Catalyst. J. Catal. 2008, 256, 338–344.
   Web of Science ®Google Scholar
• Zhu, H. Z.; Lu, Y. M.; Fan, F. J.; Yu, S. H. Selective Hydrogenation of Nitroaromatics by Ceria Nanorods. Nanoscale. 2013, 5, 7219–7223. DOI: 10.1039/c3nr02662k.
   PubMed Web of Science ®Google Scholar
• Vile, G.; Wrabetz, S.; Floryan, L.; Schuster, M. E.; Girgsdies, F.; Teschner, D.; Perez-Ramírez, J. Stereo- and Chemoselective Character of Supported CeO2 Catalysts for Continuous-Flow Three-Phase Alkyne Hydrogenation. ChemCatChem. 2014, 6, 1928–1934. DOI: 10.1002/cctc.201402124.
   Web of Science ®Google Scholar
• Shi, X.; Wang, X.; Shang, X.; Zou, X.; Ding, W.; Lu, X. High Performance and Active Sites of a Ceria‐Supported Palladium Catalyst for Solvent‐Free Chemoselective Hydrogenation of Nitroarenes. ChemCatChem. 2017, 9, 3743–3751. DOI: 10.1002/cctc.201700631.
   Web of Science ®Google Scholar
• Wei, Q.; Ma, Q.; Zuo, P.; Fan, H.; Qu, S.; Shen, W. Hollow Structure and Electron Promotion Effect of Mesoporous Pd/CeO2 Catalyst for Enhanced Catalytic Hydrogenation. ChemCatChem. 2018, 10, 1019–1026. DOI: 10.1002/cctc.201701457.
   Web of Science ®Google Scholar
• Shukla, A.; Singha, R. K.; Sasaki, T; Bal, R. Nanocrystalline Pt-CeO2 as an Efficient Catalyst for a Room Temperature Selective Reduction of Nitroarenes. Green Chem. 2015, 17, 785–790. DOI 10.1039/C4GC01664E.
   Web of Science ®Google Scholar
• She, W.; Qi, T.; Cui, M.; Yan, P.; Ng, S. W.; Li, W.; Li, G. High Catalytic Performance of a CeO2-supported Ni Catalyst for Hydrogenation of Nitroarenes, Fabricated via Coordination-assisted Strategy. ACS Appl. Mater. Interfaces. 2018, 10, 14698–14707. DOI: 10.1021/acsami.8b01187.
   PubMed Web of Science ®Google Scholar
• Hao, P.; Xie, M.; Chen, S.; Li, M.; Bi, F.; Zhang, Y.; Lin, M.; Guo, X.; Ding, W.; Guo, X. Surrounded Catalysts Prepared by Ion-exchange Inverse Loading. Sci. Adv. 2020, 6, 7031–7040. DOI 10.1126/sciadv.aay7031.
   Web of Science ®Google Scholar
• Makosch, M.; Sa, J.; Kartusch, C.; Richner, G.; van Bokhoven, J. A.; Hungerbühler, K. Hydrogenation of Nitrobenzene over Au/MeOx Catalysts—A Matter of the Support. ChemCatChem. 2012, 4, 59–63. DOI: 10.1002/cctc.201100299.
   Web of Science ®Google Scholar
• Li, H. Q.; Liu, X.; Zhang, Q.; Li, S. S.; Liu, Y. M.; He, H. Y.; Cao, Y. Deoxygenative Coupling of Nitroarenes for the Synthesis of Aromatic Azo Compounds with CO Using Supported Gold Catalysts. Chem. Commun. 2015, 51, 11217–11220. DOI: 10.1039/C5CC03134F.
   PubMed Web of Science ®Google Scholar
• Li, J.; Song, S.; Long, Y.; Wu, L.; Wang, X.; Xing, Y.; Zhang, H.; Liu, X.; Zhang, H. Investigating the Hybrid-Structure-Effect of CeO 2 -encapsulated Au Nanostructures on the transfer Coupling of nitrobenzene. Adv. Mater. 2018, 30, 1704416–1704422. DOI: 10.1002/adma.201704416.
   Web of Science ®Google Scholar
• Liu, X.; Ye, S.; Li, H. Q.; Liu, Y. M.; Cao, Y.; Fan, K. N. Mild, Selective and Switchable Transfer Reduction of Nitroarenes Catalysed by Supported Gold Nanoparticles. Catal. Sci. Technol. 2013, 3, 3200–3206. DOI: 10.1039/c3cy00533j.
   Web of Science ®Google Scholar
• Combita, D.; Concepción, P.; Corma, A. Gold Catalysts for the Synthesis of Aromatic Azocompounds from Nitroaromatics in One Step. J. Catal. 2014, 311, 339–349. DOI: 10.1016/j.jcat.2013.12.014.
   Web of Science ®Google Scholar
• Bailie, J. E.; Hutchings, G. J., and O’Leary, S. Supported Catalysts. Encyclopedia of Materials: Science and Technology; Elsevier Amsterdam; The Netherlands, 2001, 8986−8990. DOI:10.1016/B0-08-043152-6/01620-X.
   Google Scholar
• Kalita, G. D.; Sarmah, P. P.; Saikia, P. K.; Saikia, L.; Das, P. Selective Hydrogenation of Nitroarenes to Amines by Ligand-assisted Pd Nanoparticles: Influence of Donor Ligands on Catalytic Activity. New J. Chem. 2019, 43, 4253–4260. DOI: 10.1039/C8NJ05932B.
   Web of Science ®Google Scholar
• Ryabchuk, P.; Agostini, G.; Pohl, M. M.; Lund, H.; Agapova, A.; Junge, H.; Junge, K.; Beller, M. Intermetallic Nickel Silicide nanocatalyst−A Non-noble Metal–based General Hydrogenation Catalyst. Sci. Adv. 2018, 4, eaat0761. DOI 10.1126/sciadv.aat0761.
   PubMed Web of Science ®Google Scholar
• Wei, N.; Zou, X.; Huang, H.; Wang, X.; Ding, W.; Lu, X. Preparation of Well‐Ordered Mesoporous‐Silica‐Supported Ruthenium Nanoparticles for Highly Selective Reduction of Functionalized Nitroarenes through Transfer Hydrogenation. Eur. J. Org. Chem. 2018, 2018, 209–214. DOI: 10.1002/ejoc.201701228.
   Web of Science ®Google Scholar
• Yu, X.; Wang, M.; Li, H. Study on the Nitrobenzene Hydrogenation over a Pd-B/SiO2 Amorphous Catalyst. Appl. Catal., A. 2000, 202, 17–22. DOI: 10.1016/S0926-860X(00)00454-3.
   Web of Science ®Google Scholar
• Liu, Z.; Li, Y.; Huang, X.; Zuo, J.; Qin, Z.; Xu, C. Preparation and Characterization of Ni-B/SiO2 Sol Amorphous Catalyst and Its Catalytic Activity for Hydrogenation of Nitrobenzene. Catal. Commun. 2016, 85, 17–21. DOI: 10.1016/j.catcom.2016.07.008.
   Web of Science ®Google Scholar
• Xu, D.; Lv, H.; Liu, B. Encapsulation of Metal Nanoparticle Catalysts within Mesoporous Zeolites and Their Enhanced Catalytic Performances: A Review. Front. Chem. 2018, 6, 550. DOI: 10.3389/fchem.2018.00550.
   PubMed Web of Science ®Google Scholar
• Zhang, J.; Wang, L.; Shao, Y.; Wang, Y.; Gates, B. C.; Xiao, F. S. A Pd@ Zeolite Catalyst for Nitroarene Hydrogenation with High Product Selectivity by Sterically Controlled Adsorption in the Zeolite Micropores. Angew. Chem. Int. Ed. 2017, 56, 9747–9751.
   PubMed Web of Science ®Google Scholar
• Zhang, Y.; Fulajtárová, K.; Kubů, M.; Mazur, M.; Hronec, M.; Čejka, J. Electronic/steric Effects in Hydrogenation of Nitroarenes over the Heterogeneous Pd@ BEA and Pd@ MWW Catalysts. Catal. Today. 2020, 345, 39–47. DOI: 10.1016/j.cattod.2019.11.020.
   Web of Science ®Google Scholar
• Cui, T. L.; Ke, W. Y.; Zhang, W. B.; Wang, H. H.; Li, X. H.; Chen, J. S. Encapsulating Palladium Nanoparticles inside Mesoporous MFI Zeolite Nanocrystals for Shape‐Selective Catalysis. Angew. Chem. Int. Ed. 2016, 55, 9178–9182. DOI 10.1002/anie.201602429.
   PubMed Web of Science ®Google Scholar
• Mazaheri, O.; Kalbasi, R. J. Preparation and Characterization of Ni/mZSM-5 Zeolite with a Hierarchical Pore Structure by Using KIT-6 as Silica Template: An Efficient Bi-functional Catalyst for the Reduction of Nitro Aromatic Compounds. RSC Adv. 2015, 5, 34398–34414. DOI 10.1039/C5RA02349A.
   Web of Science ®Google Scholar
• Romanazzi, G.; Mastrorilli, P.; Latronico, M.; Mali, M.; Nacci, A.; Delľanna, M. M. Catalytic Activities of Heterogeneous Catalysts Obtained by Copolymerization of Metal-containing 2-(acetoacetoxy) Ethyl Methacrylate. Open Chem. 2018, 16, 520–534. DOI: 10.1515/chem-2018-0055.
   Web of Science ®Google Scholar
• Schlick, S.; Bortel, E.; Dyrek, K. Catalysis on Polymer Supports. Acta Polym. 1996, 47, 1–15. DOI: 10.1002/actp.1996.010470101.
   Google Scholar
• Sreedhar, B.; Devi, D. K.; Yada, D. Selective Hydrogenation of Nitroarenes Using Gum Acacia Supported Pt Colloid an Effective Reusable Catalyst in Aqueous Medium. Catal. Commun. 2011, 12, 1009–1014. DOI: 10.1016/j.catcom.2011.02.027.
   Web of Science ®Google Scholar
• Dell’Anna, M. M.; Intini, S.; Romanazzi, G.; Rizzuti, A.; Leonelli, C.; Piccinni, F.; Mastrorilli, P. Polymer Supported Palladium Nanocrystals as Efficient and Recyclable Catalyst for the Reduction of Nitroarenes to Anilines under Mild Conditions in Water. J. Mol. Catal. A Chem. 2014, 395, 307–314. DOI 10.1016/j.molcata.2014.08.033.
   Google Scholar
• Romanazzi, G.; Fiore, A. M.; Mali, M.; Rizzuti, A.; Leonelli, C.; Nacci, A.; Mastrorilli, P.; Dell’Anna, M. M. Polymer Supported Nickel Nanoparticles as Recyclable Catalyst for the Reduction of Nitroarenes to Anilines in Aqueous Medium. Mol. Catal. 2018, 446, 31–38.
   Google Scholar
• Dell’Anna, M. M.; Gallo, V.; Mastrorilli, P.; Romanazzi, G. A Recyclable Nanoparticle-supported Rhodium Catalyst for Hydrogenation Reactions. Molecules. 2010, 15, 3311–3318. DOI 10.3390/molecules15053311.
   PubMed Web of Science ®Google Scholar
• Wen, H.; Yao, K.; Zhang, Y.; Zhou, Z.; Kirschning, A. Catalytic Transfer Hydrogenation of Aromatic Nitro Compounds in Presence of Polymer-supported Nano-amorphous Ni–B Catalyst. Catal. Commun. 2009, 10, 1207–1211. DOI: 10.1016/j.catcom.2009.01.030.
   Web of Science ®Google Scholar
• Chu, C.; Su, Z. Facile Synthesis of AuPt Alloy Nanoparticles in Polyelectrolyte Multilayers with Enhanced Catalytic Activity for Reduction of 4-nitrophenol. Langmuir. 2014, 30, 15345–15350. DOI 10.1021/la5042019.
   PubMed Web of Science ®Google Scholar
• Doherty, S.; Knight, J. G.; Backhouse, T.; Bradford, A.; Saunders, F.; Bourne, R. A.; Chamberlain, T. W.; Stones, R.; Clayton, A.; Lovelock, K. Highly Efficient Aqueous Phase Reduction of Nitroarenes Catalysed by Phosphine-decorated Polymer Immobilized Ionic Liquid Stabilized PdNPs. Catal. Sci. Technol. 2018, 8, 1454–1467. DOI: 10.1039/C7CY02557B.
   Web of Science ®Google Scholar
• Lei, Y.; Chen, Z.; Lan, G.; Wang, R.; Zhou, X. Y. Pd Nanoparticles Stabilized with Phosphine-functionalized Porous Ionic Polymer for Efficient Catalytic Hydrogenation of Nitroarenes in Water. New J. Chem. 2020, 44, 3681–3689. DOI 10.1039/C9NJ05734J.
   Web of Science ®Google Scholar
• Li, J.; Wang, Y.; Jin, X.; Wang, Y.; Li, H. Poly (Amic Acid) Salt‐mediated Palladium and Platinum Nanoparticles as Highly Active and Recyclable Catalysts for Hydrogenation of Nitroarenes in Water under Ambient Conditions. Appl. Organomet. Chem. 2019, 33, e4717. DOI: 10.1002/aoc.4717.
   Web of Science ®Google Scholar
• Wang, X.; Huang, C.; Li, X.; Xie, C.; Yu, S. PVA‐encapsulated Palladium Nanoparticles: Eco‐friendly and Highly Selective Catalyst for Hydrogenation of Nitrobenzene in Aqueous Medium. Chem. Asian J. 2019, 14, 2266–2272. DOI: 10.1002/asia.201900333.
   PubMed Web of Science ®Google Scholar
• Guo, M.; Li, H.; Ren, Y.; Ren, X.; Yang, Q.; Li, C. Improving Catalytic Hydrogenation Performance of Pd Nanoparticles by Electronic Modulation Using Phosphine Ligands. ACS Catal. 2018, 8, 6476–6485.
   Web of Science ®Google Scholar
• Xu, K.; Zhang, Y.; Chen, X.; Huang, L.; Zhang, R.; Huang, J. Convenient and Selective Hydrogenation of Nitro Aromatics with a Platinum Nanocatalyst under Ambient Pressure. Adv. Synth. Catal. 2011, 353, 1260–1264. DOI: 10.1002/adsc.201100007.
   Web of Science ®Google Scholar
• Magdalene, R. M.; Leelamani, E. G.; Gowda, N. N. Hydrogenation of Nitroarenes Using Polybenzimidazole-supported Rhodium Catalyst. J. Mol. Catal. A Chem. 2004, 223, 17–20. DOI 10.1016/j.molcata.2003.12.041.
   Google Scholar
• Cárdenas-Lizana, F.; Berguerand, C.; Yuranov, I.; Kiwi-Minsker, L. Chemoselective Hydrogenation of Nitroarenes: Boosting Nanoparticle Efficiency by Confinement within Highly Porous Polymeric Framework. J. Catal. 2013, 301, 103–111. DOI 10.1016/j.jcat.2013.01.021.
   Web of Science ®Google Scholar
• Sadjadi, S.; Koohestani, F. Pd Immobilized on Polymeric Network Containing Imidazolium Salt, Cyclodextrin and Carbon Nanotubes: Efficient and Recyclable Catalyst for the Hydrogenation of Nitroarenes in Aqueous Media. J. Mol. Liq. 2020, 301, 112414. DOI 10.1016/j.molliq.2019.112414.
   Web of Science ®Google Scholar
• Cai, X.; Nie, J.; Yang, G.; Wang, F.; Ma, C.; Lu, C.; Chen, Z. Phosphorus-rich Network Polymer Supported Ruthenium Nanoparticles for Nitroarene Reduction. Mater. Lett. 2019, 240, 80–83. DOI 10.1016/j.matlet.2018.12.140.
   Web of Science ®Google Scholar
• Guo, M.; Li, H.; Ren, Y.; Ren, X.; Yang, Q.; Li, C. Improving Catalytic Hydrogenation Performance of Pd Nanoparticles by Electronic Modulation Using Phosphine Ligands. ACS Catal. 2018, 8, 6476–6485. DOI: 10.1021/acscatal.8b00872.
   Web of Science ®Google Scholar
• Ding, S. Y.; Wang, W. Covalent Organic Frameworks (Cofs): From Design to Applications. Chem. Soc. Rev. 2013, 42, 548–568. DOI: 10.1039/C2CS35072F.
   PubMed Web of Science ®Google Scholar
• Zeng, Y.; Zou, R.; Luo, Z.; Zhang, H.; Yao, X.; Ma, X.; Zou, R.; Zhao, Y. Covalent Organic Frameworks Formed with Two Types of Covalent Bonds Based on Orthogonal Reactions. J. Am. Chem. Soc. 2015, 137, 1020–1023. DOI 10.1021/ja510926w.
   PubMed Web of Science ®Google Scholar
• Huang, N.; Chen, X.; Krishna, R.; Jiang, D. Two‐dimensional Covalent Organic Frameworks for Carbon Dioxide Capture through Channel‐wall Functionalization. Angew. Chem. Int. Ed. 2015, 54, 2986–2990.
   PubMed Web of Science ®Google Scholar
• Gomes, R.; Bhanja, P.; Bhaumik, A. A Triazine-based Covalent Organic Polymer for Efficient CO2 Adsorption. Chem. Commun. 2015, 51, 10050–10053. DOI 10.1039/C5CC02147B.
   PubMed Web of Science ®Google Scholar
• Li, Z.; Feng, X.; Zou, Y.; Zhang, Y.; Xia, H.; Liu, X.; Mu, Y. A 2D Azine-linked Covalent Organic Framework for Gas Storage Applications. Chem. Commun. 2014, 50, 1382–13825. DOI: 10.1039/C4CC05665E.
   Web of Science ®Google Scholar
• Vijay, S. V.; Medhavi, V.; Igor, M.; Frederik, H.; Gokcen, S.; Christian, O.; Joachim, P. S.; Bettina, V. L. Exploiting Noncovalent Interactions in an Imine-Based Covalent Organic Framework for Quercetin Delivery. Adv. Mater. 2016, 28, 8749–8754. DOI 10.1002/adma.201603006.
   PubMed Web of Science ®Google Scholar
• Stegbauer, L.; Schwinghammer, K.; Lotsch, B. V. A Hydrazone-based Covalent Organic Framework for Photocatalytic Hydrogen Production. Chem. Sci. 2014, 5, 2789–2793. DOI: 10.1039/C4SC00016A.
   Web of Science ®Google Scholar
• Liu, G.; Sheng, J.; Zhao, Y. Chiral Covalent Organic Frameworks for Asymmetric Catalysis and Chiral Separation. Sci. China: Chem. 2017, 60, 1015–1022. DOI: 10.1007/s11426-017-9070-1.
   Web of Science ®Google Scholar
• Long, J.; Liu, H.; Wu, S.; Liao, S.; Li, Y. Selective Oxidation of Saturated Hydrocarbons Using Au–Pd Alloy Nanoparticles Supported on Metal–organic Frameworks. ACS Catal. 2013, 3, 647–654. DOI: 10.1021/cs300754k.
   Web of Science ®Google Scholar
• Sadhasivam, V.; Mariyappan, M.; Siva, A. Porous Triazine Containing Covalent Organic Polymer Supported Pd Nanoparticles: A Stable and Efficient Heterogeneous Catalyst for Sonogashira Cross‐Coupling and the Reduction of Nitroarenes. ChemistrySelect. 2018, 3, 13442–13455. DOI: 10.1002/slct.201802977.
   Web of Science ®Google Scholar
• Yuan, M.; Yang, R.; Wei, S.; Hu, X.; Xu, D.; Yang, J.; Dong, Z. Ultra-fine Pd Nanoparticles Confined in A Porous Organic Polymer: A Leaching-and-aggregation-resistant Catalyst for the Efficient Reduction of Nitroarenes by NaBH4. J. Colloid Interface Sci. 2019, 538, 720–730. DOI: 10.1016/j.jcis.2018.11.065.
   PubMed Web of Science ®Google Scholar
• Li, J.; Zhang, L.; Liu, X.; Shang, N.; Gao, S.; Feng, C.; Wang, C.; Wang, Z. Pd Nanoparticles Supported on a Covalent Triazine-based Framework Material: An Efficient and Highly Chemoselective Catalyst for the Reduction of Nitroarenes. New J. Chem. 2018, 42, 9684–9689.
   Web of Science ®Google Scholar
• Shi, X.; Yao, Y.; Xu, Y.; Liu, K.; Zhu, G.; Chi, L.; Lu, G. Imparting Catalytic Activity to a Covalent Organic Framework Material by Nanoparticle Encapsulation. ACS Appl. Mater. Interfaces. 2017, 9, 7481–7488. DOI: 10.1021/acsami.6b16267.
   PubMed Web of Science ®Google Scholar
• Emadi, F.; Nemati, F; Elhampour, A. Silver Nanoparticles Supported on Mesoporous Triazine Carbon Material: A Versatile Catalyst for Reduction of Nitroaromatic Compounds. ChemistrySelect. 2020, 5, 4328–4336. DOI 10.1002/slct.202000645.
   Web of Science ®Google Scholar
• Rodríguez‐San‐Miguel, D.; Yazdi, A.; Guillerm, V. J. P.; Puntes, V.; Maspoch, D.; Zamora, F.; Zamora, F. Confining Functional Nanoparticles into Colloidal Imine‐Based COF Spheres by a Sequential Encapsulation–Crystallization Method. Chem. - Eur. J. 2017, 23, 8623–8627. DOI 10.1002/chem.201702072.
   PubMed Web of Science ®Google Scholar
• Yaghi, O. M.; Li, H. Hydrothermal Synthesis of a Metal-organic Framework Containing Large Rectangular Channels. J. Am. Chem. Soc. 1995, 117, 10401–10402. DOI 10.1021/ja00146a033.
   Web of Science ®Google Scholar
• Subramanian, S.; Zaworotko, M. J. Porous Solids by design:[Zn (4,4′‐bpy)2(sif 6)]n·xDMF, a Single Framework Octahedral Coordination Polymer with Large Square Channels. Angew. Chem. Int. Ed. Engl. 1995, 34, 2127–2129. DOI 10.1002/anie.199521271.
   Web of Science ®Google Scholar
• Kepert, C. J.; Rosseinsky, M. J. A Porous Chiral Framework of Coordinated 1, 3, 5-benzenetricarboxylate: Quadruple Interpenetration of the (10, 3)-A Network. Chem. Commun. 1998, 31–32. doi:10.1039/a705336c.
   Web of Science ®Google Scholar
• Janiak, C.; Vieth, J. K. MOFs, MILs and More: Concepts, Properties and Applications for Porous Coordination Networks (Pcns). New J. Chem. 2010, 34, 2366–2388.
   Web of Science ®Google Scholar
• Kim, C. R.; Uemura, T; Kitagawa, S. Inorganic Nanoparticles in Porous Coordination Polymers. Chem. Soc. Rev. 2016, 45, 3828–3845. DOI 10.1039/C5CS00940E.
   PubMed Web of Science ®Google Scholar
• Zhao, D.; Timmons, D. J.; Yuan, D.; Zhou, H. C. Tuning the Topology and Functionality of Metal− Organic Frameworks by Ligand Design. Acc. Chem. Res. 2011, 44, 123–133. DOI: 10.1021/ar100112y.
   PubMed Web of Science ®Google Scholar
• Cohen, S. M. Postsynthetic Methods for the Functionalization of Metal–organic Frameworks. Chem. Rev. 2012, 112, 970–1000. DOI: 10.1021/cr200179u.
   PubMed Web of Science ®Google Scholar
• Lin, Z. J.; Lü, J.; Hong, M.; Cao, R. Metal–organic Frameworks Based on Flexible Ligands (Fl-mofs): Structures and Applications. Chem. Soc. Rev. 2014, 43, 5867–5895. DOI: 10.1039/C3CS60483G.
   PubMed Web of Science ®Google Scholar
• Liu, J.; Chen, L.; Cui, H.; Zhang, J.; Zhang, L.; Su, C. Y. Applications of Metal–organic Frameworks in Heterogeneous Supramolecular Catalysis. Chem. Soc. Rev. 2014, 43, 6011–6061. DOI: 10.1039/C4CS00094C.
   PubMed Web of Science ®Google Scholar
• Dhakshinamoorthy, A.; Asiri, A. M.; Garcia, H. Metal–organic Frameworks Catalysed C–C and C–heteroatom Coupling Reactions. Chem. Soc. Rev. 2015, 44, 1922–1947. DOI: 10.1039/C4CS00254G.
   PubMed Web of Science ®Google Scholar
• Huang, Y. B.; Liang, J.; Wang, X. S.; Cao, R. Multifunctional Metal–organic Framework Catalysts: Synergistic Catalysis and Tandem Reactions. Chem. Soc. Rev. 2017, 46, 126–157. DOI: 10.1039/C6CS00250A.
   PubMed Web of Science ®Google Scholar
• Liu, Y.; Xuan, W.; Cui, Y. Engineering Homochiral Metal‐organic Frameworks for Heterogeneous Asymmetric Catalysis and Enantioselective Separation. Adv. Mater. 2010, 22, 4112–4135. DOI: 10.1002/adma.201000197.
   PubMed Web of Science ®Google Scholar
• Zhang, T.; Lin, W. Metal–organic Frameworks for Artificial Photosynthesis and Photocatalysis. Chem. Soc. Rev. 2014, 43, 5982–5993. DOI: 10.1039/C4CS00103F.
   PubMed Web of Science ®Google Scholar
• Jian, S.; Li, Y. Ni@ Pd Core-shell Nanoparticles Supported on a Metal-organic Framework as Highly Efficient Catalysts for Nitroarenes Reduction. Chin. J. Catal. 2016, 37, 91–97. DOI 10.1016/S1872-2067(15)60940-8.
   Web of Science ®Google Scholar
• Ji, P.; Manna, K.; Lin, Z.; Feng, X.; Urban, A.; Song, Y.; Lin, W. Single-site Cobalt Catalysts at New Zr12(μ3-O)8(μ3-OH)8(μ2-OH)6 Metal–organic Framework Nodes for Highly Active Hydrogenation of Nitroarenes, Nitriles, and Isocyanides. J. Am. Chem. Soc. 2017, 139, 7004–7011. DOI 10.1021/jacs.7b02394.
   PubMed Web of Science ®Google Scholar
• Bao, L.; Yu, Z.; Fei, T.; Yan, Z.; Li, J.; Sun, C.; Pang, S. Palladium Supported on Metal–organic Framework as a Catalyst for the Hydrogenation of Nitroarenes under Mild Conditions. Appl. Organomet. Chem. 2020, 34, e5607. DOI 10.1002/aoc.5607.
   Web of Science ®Google Scholar
• Zhou, Y. H.; Yang, Q.; Chen, Y. Z.; Jiang, H. L. Low-cost CuNi@ MIL-101 as an Excellent Catalyst toward Cascade Reaction: Integration of Ammonia Borane Dehydrogenation with Nitroarene Hydrogenation. Chem. Commun. 2017, 53, 12361–12364. DOI: 10.1039/C7CC06530B.
   PubMed Web of Science ®Google Scholar
• Sun, J. L.; Chen, Y. Z.; Ge, B. D.; Li, J. H. J. H; Wang, G. M. Three-shell Cu@ Co@ Ni Nanoparticles Stabilized with a Metal–organic Framework for Enhanced Tandem Catalysis. ACS Appl. Mater. Interfaces. 2018, 11, 940–947. DOI: 10.1021/acsami.8b18584.
   PubMed Web of Science ®Google Scholar
• Babel, V.; Hiran, B. L. Heterogeneous AgPd Alloy Nanocatalyst for Selective Reduction of Aromatic Nitro Compounds Using Formic Acid as Hydrogen Source. Catal. Lett. 2020, 150, 1865–1869. DOI: 10.1007/s10562-020-03098-y.
   Web of Science ®Google Scholar
• Jiang, H. L.; Akita, T.; Ishida, T.; Haruta, M.; Xu, Q. Synergistic Catalysis of Au@ Ag Core− Shell Nanoparticles Stabilized on Metal− Organic Framework. J. Am. Chem. Soc. 2011, 133, 1304–1306. DOI 10.1021/ja1099006.
   PubMed Web of Science ®Google Scholar
• Pachfule, P.; Kandambeth, S.; Díaz, D. D.; Banerjee, R. Highly Stable Covalent Organic framework–Au Nanoparticles Hybrids for Enhanced Activity for Nitrophenol Reduction. Chem. Commun. 2014, 50, 3169–3172. DOI: 10.1039/C3CC49176E.
   PubMed Web of Science ®Google Scholar
• Yang, Q.; Zhang, H. Y.; Wang, L.; Zhang, Y.; Zhao, J. Ru/UiO-66 Catalyst for the Reduction of Nitroarenes and Tandem Reaction of Alcohol oxidation/Knoevenagel Condensation. ACS omega. 2018, 3, 4199–4212. DOI: 10.1021/acsomega.8b00157.
   PubMed Web of Science ®Google Scholar
• Zhuang, G. L.; Bai, J. Q.; Tan, L.; Huang, H. L.; Gao, Y. F.; Zhong, X.; Zhong, C. L.; Wang, J. G. Preparation and Catalytic Properties of Pd Nanoparticles Supported on Micro-crystal DUT-67 MOFs. RSC Adv. 2015, 5, 32714–32719. DOI: 10.1039/C5RA03286E.
   Web of Science ®Google Scholar
• Jiao, N.; Li, Z.; Xia, C.; Liu, J. Palladium Nanoparticles Immobilized on Cross‐Linked Polymeric Ionic Liquid Material: Application as Efficient and Recoverable Catalyst for the Hydrogenation of Nitroarenes. ChemistrySelect. 2017, 2, 4545–4556. DOI 10.1002/slct.201700836.
   Web of Science ®Google Scholar
• Du, W.; Chen, G.; Nie, R.; Li, Y.; Hou, Z. Highly Dispersed Pt in MIL-101: An Efficient Catalyst for the Hydrogenation of Nitroarenes. Catal. Commun. 2013, 41, 56–59. DOI: 10.1016/j.catcom.2013.06.038.
   Web of Science ®Google Scholar
• Guha, N. R.; Bhattacherjee, D.; Das, P. Solid Supported Rhodium (0) Nanoparticles: An Efficient Catalyst for Chemo-and Regio-selective Transfer Hydrogenation of Nitroarenes to Anilines under Microwave Irradiation. Tetrahedron Lett. 2014, 55, 2912–2916. DOI: 10.1016/j.tetlet.2014.03.047.
   Web of Science ®Google Scholar
• Yadav, V.; Gupta, S.; Kumar, R.; Singh, G.; Lagarkha, R. Polymeric Peg35k-pd Nanoparticles: Efficient and Recyclable Catalyst for Reduction of Nitro Compounds. Synth. Commun. 2012, 42, 213–222. DOI: 10.1080/00397911.2010.523159.
   Web of Science ®Google Scholar
• Salam, N.; Banerjee, B.; Roy, A. S.; Mondal, P.; Roy, S.; Bhaumik, A.; Islam, S. M. Silver Nanoparticles Embedded over Mesoporous Organic Polymer as Highly Efficient and Reusable Nanocatalyst for the Reduction of Nitroarenes and Aerobic Oxidative Esterification of Alcohols. Appl. Catal., A. 2014, 477, 184–194. DOI 10.1016/j.apcata.2014.03.014.
   Web of Science ®Google Scholar
• Ding, Z. C.; Li, C. Y.; Chen, J. J.; Zeng, J. H.; Tang, H. T.; Ding, Y. J.; Zhan, Z. P. Palladium/Phosphorus‐Doped Porous Organic Polymer as Recyclable Chemoselective and Efficient Hydrogenation Catalyst under Ambient Conditions. Adv. Synth. Catal. 2017, 359, 2280–2287. DOI: 10.1002/adsc.201700374.
   Web of Science ®Google Scholar
• Li, L.; Zhou, C.; Zhao, H.; Wang, R. Spatial Control of Palladium Nanoparticles in Flexible Click-based Porous Organic Polymers for Hydrogenation of Olefins and Nitrobenzene. Nano Res. 2015, 8, 709–721.
   Web of Science ®Google Scholar