Sadjadi Samahe, Heydari Abolfazl
Gas Conversion Department, Faculty of Petrochemicals, Iran Polymer and Petrochemical Institute, P.O. Box 14975-112, Tehran 14977-13115, Iran.
Polymer Institute of the Slovak Academy of Sciences, Dúbravská cesta 9, 845 41 Bratislava, Slovakia.
Polymers (Basel). 2023 Jul 29;15(15):3240. doi: 10.3390/polym15153240.
In this study, we present a novel composite material consisting of β-cyclodextrin nanosponge and sodium alginate, used as a support for the immobilization of palladium (Pd) nanoparticles. The composite alginate-cyclodextrin nanosponge beads were prepared, taking advantage of the 3D polymeric network and β-cyclodextrin cavity of the nanosponge. These beads exhibited excellent encapsulation capabilities for hydrophobic substrates, allowing their transfer in aqueous media. The cyclodextrin nanosponge served as a stabilizer for Pd nanoparticles and facilitated phase transfer. Additionally, the sodium alginate bead contributed to the robustness of the structure and improved the recovery and recyclability of the composite material. Comparative studies with control catalysts confirmed the beneficial effect of incorporating cyclodextrin nanosponge within alginate beads, particularly for more hydrophobic substrates. Optimization of reaction conditions revealed that employing 0.03 g of catalyst per mmol of nitroarene at 45 °C resulted in the maximum yield within 90 min. Evaluation of the substrate scope demonstrated the hydrogenation capability of various substrates with different electronic properties under the developed protocol. Notably, the nitro group was selectively reduced in substrates featuring competing functionalities. Furthermore, the recyclability and stability of the composite catalyst were confirmed, making it a promising candidate for sustainable catalysis.
在本研究中,我们展示了一种由β-环糊精纳米海绵和海藻酸钠组成的新型复合材料,用作固定钯(Pd)纳米颗粒的载体。利用纳米海绵的三维聚合物网络和β-环糊精腔体制备了复合海藻酸钠-环糊精纳米海绵珠。这些珠子对疏水底物表现出优异的包封能力,使其能够在水性介质中转移。环糊精纳米海绵作为钯纳米颗粒的稳定剂并促进相转移。此外,海藻酸钠珠有助于结构的坚固性,并提高了复合材料的回收率和可回收性。与对照催化剂的比较研究证实了在海藻酸钠珠中加入环糊精纳米海绵的有益效果,特别是对于疏水性更强的底物。反应条件的优化表明,在45℃下每毫摩尔硝基芳烃使用0.03 g催化剂,在90分钟内可获得最大产率。底物范围的评估表明,在已开发的方案下,各种具有不同电子性质的底物具有氢化能力。值得注意的是,在具有竞争官能团的底物中硝基被选择性还原。此外,复合催化剂的可回收性和稳定性得到了证实,使其成为可持续催化的有前途的候选者。