Ni nanowires decorated with Pd nanoparticles as an efficient nanocatalytic system for Suzuki coupling of anisole derivatives
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[1] C. Schulzke,et al. Phosphine ligands based on the ferrocenyl platform: Advances in catalytic cross-couplings , 2023, Coordination Chemistry Reviews.
[2] Ho Won Jang,et al. Metal-organic framework-based nanostructured catalysts: Applications in efficient organic transformations , 2023, Molecular Catalysis.
[3] Ho Won Jang,et al. Recent catalytic applications of MXene-based layered nanomaterials. , 2023, Chemosphere.
[4] Yong-Jun Li,et al. Nanoarchitectonics of 2D-thin and porous Ag-Au nanostructures with controllable alloying degrees toward electrocatalytic CO2 reduction , 2023, Journal of Alloys and Compounds.
[5] Z. Tang,et al. Nanostructural engineering of metal-organic frameworks: Construction strategies and catalytic applications , 2022, Matter.
[6] M. Rabbani,et al. A retrospective-prospective review of Suzuki–Miyaura reaction: From cross-coupling reaction to pharmaceutical industry applications , 2022, Polyhedron.
[7] Rong-Lin Zhong,et al. Atropisomeric Phosphine Ligands Bearing C-N Axial Chirality: Applications in Enantioselective Suzuki-Miyaura Cross-Coupling Towards the Assembly of Tetra-ortho-Substituted Biaryls. , 2022, Journal of the American Chemical Society.
[8] Yingwei Li,et al. Ordered macroporous MOF-based materials for catalysis , 2022, Molecular Catalysis.
[9] Ho Won Jang,et al. Emerging Two-Dimensional-Based Nanostructured Catalysts: Applications in Sustainable Organic Transformations. , 2022, Langmuir : the ACS journal of surfaces and colloids.
[10] H. Garmestani,et al. Hydrothermal synthesis and water splitting application of d-Ti3C2 MXene/V2O5 hybrid nanostructures as an efficient bifunctional catalyst , 2022, International Journal of Hydrogen Energy.
[11] O. Reiser,et al. Dendritic structured palladium complexes: magnetically retrievable, highly efficient heterogeneous nanocatalyst for Suzuki and Heck cross-coupling reactions , 2022, RSC advances.
[12] D. Janas,et al. Nanowires as a versatile catalytic platform for facilitating chemical transformations , 2022, Journal of Alloys and Compounds.
[13] Lang Ma,et al. Emerging 2D Materials for Electrocatalytic Applications: Synthesis, Multifaceted Nanostructures, and Catalytic Center Design. , 2022, Small.
[14] H. Zeng,et al. Nanowire Networks of Metal–Organosilicates as Reversible Pd(II) Reservoirs for Suzuki Coupling Reactions , 2021, ACS Applied Nano Materials.
[15] R. Luque,et al. Sustainable and recyclable heterogenous palladium catalysts from rice husk-derived biosilicates for Suzuki-Miyaura cross-couplings, aerobic oxidations and stereoselective cascade carbocyclizations , 2020, Scientific Reports.
[16] Ho Won Jang,et al. Palladium Nanoparticles on Assorted Nanostructured Supports: Applications for Suzuki, Heck, and Sonogashira Cross-Coupling Reactions , 2020 .
[17] T. Honma,et al. Ligand-free Suzuki–Miyaura coupling reaction of an aryl chloride using a continuous irradiation type microwave and a palladium nanoparticle catalyst: effect of a co-existing solid , 2019, Green Chemistry.
[18] Hongpeng Ma,et al. Heterogeneous Suzuki–Miyaura coupling of heteroaryl ester via chemoselective C(acyl)–O bond activation , 2019, RSC advances.
[19] J. M. Tengco,et al. A Molecular/Heterogeneous Nickel Catalyst for Suzuki–Miyaura Coupling , 2019, Organometallics.
[20] M. S. Hegde,et al. Recyclable Pd ionic catalyst coated on cordierite monolith for high TOF Heck coupling reaction , 2019, Journal of Chemical Sciences.
[21] D. Janas,et al. Nickel Nanowires: Synthesis, Characterization and Application as Effective Catalysts for the Reduction of Nitroarenes , 2018, Catalysts.
[22] Y. Tamenori,et al. Reusable Immobilized Iron(II) Nanoparticle Precatalysts for Ligand-Free Kumada Coupling , 2018, ACS Applied Nano Materials.
[23] S. Bhattacharya,et al. Size-Dependent Catalytic Activity and Fate of Palladium Nanoparticles in Suzuki–Miyaura Coupling Reactions , 2018, ACS omega.
[24] P. Midgley,et al. A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling , 2018, Nature Nanotechnology.
[25] C. Subrahmanyam,et al. Recyclable Pd/CuFe2O4 nanowires: a highly active catalyst for C–C couplings and synthesis of benzofuran derivatives , 2018, RSC advances.
[26] Jingguang G. Chen,et al. Understanding the Role of M/Pt(111) (M = Fe, Co, Ni, Cu) Bimetallic Surfaces for Selective Hydrodeoxygenation of Furfural , 2017 .
[27] M. Klinger. More features, more tools, more CrysTBox , 2017 .
[28] J. Polanski,et al. Oxide passivated Ni-supported Ru nanoparticles in silica: A new catalyst for low-temperature carbon dioxide methanation , 2017 .
[29] L. Tang,et al. Pd–ZnO nanowire arrays as recyclable catalysts for 4-nitrophenol reduction and Suzuki coupling reactions , 2017 .
[30] Ya‐Ping Sun,et al. Boron Nitride Nanosheet-Anchored Pd-Fe Core-Shell Nanoparticles as Highly Efficient Catalysts for Suzuki-Miyaura Coupling Reactions. , 2017, ACS applied materials & interfaces.
[31] Zaizhu Lou,et al. Promoting Pd-catalyzed Suzuki coupling reactions through near-infrared plasmon excitation of WO3−x nanowires , 2016 .
[32] Yongfeng Li,et al. Pd/PdO nanoparticles supported on carbon nanotubes: A highly effective catalyst for promoting Suzuki reaction in water , 2015 .
[33] Miloslav Klinger,et al. Crystallographic Tool Box (CrysTBox): automated tools for transmission electron microscopists and crystallographers , 2015, Journal of applied crystallography.
[34] X. Bai,et al. Novel Pd Nanocubes Supported on Activated Carbon as a Catalyst for theSuzuki-Miyaura Coupling Reaction , 2015 .
[35] Isidro M. Pastor,et al. Palladium nanoparticles supported on graphene and reduced graphene oxide as efficient recyclable catalyst for the Suzuki–Miyaura reaction of potassium aryltrifluoroborates , 2015 .
[36] M. Shelke,et al. A green approach for the decoration of Pd nanoparticles on graphene nanosheets: An in situ process for the reduction of C–C double bonds and a reusable catalyst for the Suzuki cross-coupling reaction , 2015 .
[37] B. Bhanage,et al. Palladacycle-Catalyzed Carbonylative Suzuki-Miyaura Coupling with High Turnover Number and Turnover Frequency. , 2015, The Journal of organic chemistry.
[38] A. Ehsani,et al. Synthesis of Au/Pd bimetallic nanoparticles and their application in the Suzuki coupling reaction , 2015 .
[39] M. Dabiri,et al. Palladium nanoparticle decorated high nitrogen-doped graphene with high catalytic activity for Suzuki–Miyaura and Ullmann-type coupling reactions in aqueous media , 2014 .
[40] A. Schmitzer,et al. Support-Free Palladium–NHC Catalyst for Highly Recyclable Heterogeneous Suzuki–Miyaura Coupling in Neat Water , 2014 .
[41] Yoichi M. A. Yamada,et al. A palladium-nanoparticle and silicon-nanowire-array hybrid: a platform for catalytic heterogeneous reactions. , 2014, Angewandte Chemie.
[42] Yadong Li,et al. Progress in organic reactions catalyzed by bimetallic nanomaterials , 2013 .
[43] Débora Micheline Vaz de Miranda,et al. Air stable ligandless heterogeneous catalyst systems based on Pd and Au supported in SiO2 and MCM-41 for Suzuki–Miyaura cross-coupling in aqueous medium , 2013 .
[44] Yongfeng Li,et al. Plasma synthesis of Pd nanoparticles decorated-carbon nanotubes and its application in Suzuki reaction , 2013 .
[45] S. Horikoshi,et al. Control of microwave-generated hot spots. Part V. Mechanisms of hot-spot generation and aggregation of catalyst in a microwave-assisted reaction in toluene catalyzed by Pd-loaded AC particulates , 2013 .
[46] Y. Sung,et al. Heterogeneous Suzuki Cross‐Coupling Reaction Catalyzed by Magnetically Recyclable Nanocatalyst. , 2013 .
[47] Haiyang Sun,et al. Palladium nanoparticles supported on functional ionic liquid modified magnetic nanoparticles as recyclable catalyst for room temperature Suzuki reaction , 2013 .
[48] D. Chand,et al. Palladium nanoparticles catalyzed Suzuki cross-coupling reactions in ambient conditions , 2013 .
[49] M. Pérez-Lorenzo. Palladium Nanoparticles as Efficient Catalysts for Suzuki Cross‐Coupling Reactions , 2012 .
[50] M. Pagliaro,et al. Heterogeneous versus Homogeneous Palladium Catalysts for Cross‐Coupling Reactions , 2012 .
[51] Nick Serpone,et al. On the Generation of Hot-Spots by Microwave Electric and Magnetic Fields and Their Impact on a Microwave-Assisted Heterogeneous Reaction in the Presence of Metallic Pd Nanoparticles on an Activated Carbon Support , 2011 .
[52] D. Song,et al. Palladium nanoparticles in carbon thin film-lined SBA-15 nanoreactors: efficient heterogeneous catalysts for Suzuki-Miyaura cross coupling reaction in aqueous media. , 2011, Chemical communications.
[53] A. Cao,et al. Stabilizing metal nanoparticles for heterogeneous catalysis. , 2010, Physical chemistry chemical physics : PCCP.
[54] M. Delamar,et al. Hairy carbon nanotube@nano-Pd heterostructures: design, characterization, and application in Suzuki C-C coupling reaction. , 2010, Langmuir : the ACS journal of surfaces and colloids.
[55] Guoliang Zhang,et al. Palladium nanoparticle-graphene hybrids as active catalysts for the Suzuki reaction , 2010 .
[56] Zhenshan Hou,et al. Ionic liquid immobilized nickel(0) nanoparticles as stable and highly efficient catalysts for selective hydrogenation in the aqueous phase. , 2010, Chemistry, an Asian journal.
[57] Xian‐Wen Wei,et al. Fe3O4 Nanoparticles-Supported Palladium-Bipyridine Complex: Effective Catalyst for Suzuki Coupling Reaction , 2010 .
[58] S. Buchwald,et al. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. , 2008, Accounts of chemical research.
[59] G. Rothenberg,et al. Ion- and atom-leaching mechanisms from palladium nanoparticles in cross-coupling reactions. , 2007, Chemistry.
[60] Y. Monguchi,et al. Heterogeneous Pd/C-catalyzed ligand-free, room-temperature Suzuki-Miyaura coupling reactions in aqueous media. , 2007, Chemistry.
[61] C. A. Russell,et al. Cyclopropenylidene carbene ligands in palladium C-C coupling catalysis. , 2007, Chemical communications.
[62] Tao Chen,et al. A novel tridentate NHC-Pd(II) complex and its application in the Suzuki and Heck-type cross-coupling reactions , 2006 .
[63] S. Schneider,et al. A carbocyclic carbene as an efficient catalyst ligand for C-C coupling reactions. , 2006, Angewandte Chemie.
[64] E. Tyrrell,et al. The Synthesis and Applications of Heterocyclic Boronic Acids , 2003 .
[65] David Gray,et al. Towards novel processes for the fine-chemical and pharmaceutical industries. , 2002, Current opinion in biotechnology.
[66] D. D. De Vos,et al. Impact of Pd-mordenite pretreatment on the heterogeneity of Heck catalysis. , 2002, Chemical communications.
[67] Stewart F. Parker,et al. Poisoning and deactivation of palladium catalysts , 2001 .
[68] T. Fujimoto,et al. Sonochemical preparation of single-dispersion metal nanoparticles from metal salts , 2001 .
[69] M. Shirai,et al. Recyclable Homogeneous/Heterogeneous Catalytic Systems for Heck Reaction through Reversible Transfer of Palladium Species between Solvent and Support , 2000 .
[70] H. Blaser. Heterogeneous catalysis for fine chemicals production , 2000 .
[71] Hong,et al. Suzuki cross-coupling reactions catalyzed by palladium nanoparticles in aqueous solution , 2000, Organic letters.
[72] G. C. Fu,et al. Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions , 2000 .
[73] H. Blaser,et al. The role of catalysis for the clean production of fine chemicals , 1999 .
[74] M. Beller,et al. Palladacycles as Efficient Catalysts for Aryl Coupling Reactions , 1995 .
[75] Norio Miyaura,et al. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides , 1980 .
[76] Q. Le,et al. Recent advances in nanoengineering 2D metal-based materials for electrocatalytic conversion of carbon dioxide into fuels and value-added products , 2023, Fuel.
[77] B. Pugin,et al. Selective Hydrogenation for Fine Chemicals: Recent Trends and New Developments , 2003 .