Ni nanowires decorated with Pd nanoparticles as an efficient nanocatalytic system for Suzuki coupling of anisole derivatives

[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 .