Palladium Nanoparticle-Embedded Polymer Thin Film “Dip Catalyst” for Suzuki–Miyaura Reaction
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[1] D. D. L. Martins,et al. Microwave-assisted Suzuki reaction catalyzed by Pd(0)–PVP nanoparticles , 2010 .
[2] Zhao,et al. Heck reactions of iodobenzene and methyl acrylate with conventional supported palladium catalysts in the presence of organic and/or inorganic bases without ligands , 2000, Chemistry.
[3] J. Ahmed,et al. Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki-Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15. , 2010, Chemical communications.
[4] Yanqing Peng,et al. Reusable Pd nanoparticles immobilized on functional ionic liquid co-polymerized with styrene for Suzuki reactions in water–ethanol solution , 2011 .
[5] Shinji Kato,et al. Palladium nanoparticles captured in microporous polymers: a tailor-made catalyst for heterogeneous carbon cross-coupling reactions. , 2010, Journal of the American Chemical Society.
[6] L. Djakovitch,et al. Heck reaction catalyzed by PD-modified zeolites. , 2001, Journal of the American Chemical Society.
[7] N. Leadbeater. Cross coupling: When is free really free? , 2010, Nature chemistry.
[8] R. Cao,et al. Synthesis of palladium nanocatalysts with cucurbit[n]uril as both a protecting agent and a support for Suzuki and Heck reactions , 2012 .
[9] Longfeng Zhu,et al. Porous polymer supported palladium catalyst for cross coupling reactions with high activity and recyclability , 2012, Science China Chemistry.
[10] G. V. Ramesh,et al. Polymer thin films embedded with in situ grown metal nanoparticles. , 2009, Chemical Society reviews.
[11] A. Ragauskas,et al. Environmentally friendly synthesis of biaryls: Suzuki reaction of aryl bromides in water at low catalyst loadings , 2006 .
[12] L. Wan,et al. In-Situ Loading of Noble Metal Nanoparticles on Hydroxyl-Group-Rich Titania Precursor and Their Catalytic Applications , 2007 .
[13] Gregory S. Smith,et al. Pd nanosized particles supported on chitosan and 6-deoxy-6-amino chitosan as recyclable catalysts for Suzuki-Miyaura and Heck cross-coupling reactions , 2011 .
[14] L. Djakovitch,et al. Supported palladium as catalyst for carbon–carbon bond construction (Heck reaction) in organic synthesis , 2001 .
[15] Maiyong Zhu,et al. Magnetically Recyclable Pd Nanoparticles Immobilized on Magnetic Fe3O4@C Nanocomposites: Preparation, Characterization, and Their Catalytic Activity toward Suzuki and Heck Coupling Reactions , 2011 .
[16] Yukihiro Motoyama,et al. Highly efficient Suzuki–Miyaura coupling reactions catalyzed by bis(oxazolinyl)phenyl–Pd(II) complex , 2007 .
[17] T. Honma,et al. Highly dispersed Pd species active in the Suzuki-Miyaura reaction. , 2009, ChemPhysChem.
[18] C. Sanchez,et al. Palladium nanoparticles heterogeneous nucleation within organically grafted silica foams and their use as catalyst supports toward the Suzuki-Miyaura and Mizoroki-Heck coupling reactions , 2010 .
[19] P. Claus,et al. Implementation of the multi-channel monolith reactor in an optimisation procedure for heterogeneous oxidation catalysts based on genetic algorithms. , 2007, Combinatorial chemistry & high throughput screening.
[20] A. Sayari,et al. Applications of pore-expanded mesoporous silica 6. Novel synthesis of monodispersed supported palladium nanoparticles and their catalytic activity for suzuki reaction , 2007 .
[21] P. Thilagar,et al. Organostannoxane-Supported Palladium Nanoparticles. Highly Efficient Catalysts for Suzuki-Coupling Reactions , 2009 .
[22] B. Sreedhar,et al. Palladium Nanowire from Precursor Nanowire: Crystal‐to‐Crystal Transformation via In Situ Reduction by Polymer Matrix , 2007 .
[23] T. Srinivasan,et al. One-pot electrochemical synthesis of palladium nanoparticles and their application in the Suzuki reaction , 2011 .
[24] Weihua Tang,et al. Bio-supported palladium nanoparticles as a phosphine -free catalyst for the Suzuki reaction in water , 2012 .
[25] D. Astruc,et al. "Homeopathic" catalytic activity and atom-leaching mechanism in Miyaura-Suzuki reactions under ambient conditions with precise dendrimer-stabilized Pd nanoparticles. , 2007, Angewandte Chemie.
[26] Qizhong Zhou,et al. Water Soluble Starch Stabilized Palladium Nanoparticle: Efficient Catalyst for Miyaura‐Suzuki Coupling Reaction , 2010 .
[27] B. Tamami,et al. Palladium nanoparticles supported on modified crosslinked polyacrylamide containing phosphinite ligand: A novel and efficient heterogeneous catalyst for carbon–carbon cross-coupling reactions , 2010 .
[28] 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.
[29] T. Radhakrishnan,et al. A highly efficient and extensively reusable "dip catalyst" based on a silver-nanoparticle-embedded polymer thin film. , 2010, Chemistry.
[30] Lei Wu,et al. Phosphine dendrimer-stabilized palladium nanoparticles, a highly active and recyclable catalyst for the Suzuki-Miyaura reaction and hydrogenation. , 2006, Organic letters.
[31] Shiyong Liu,et al. Dodecylsulfate Anion Embedded Layered Double Hydroxide Supported Nanopalladium Catalyst for the Suzuki Reaction , 2010 .
[32] R. Clérac,et al. Dendron-functionalized core-shell superparamagnetic nanoparticles: magnetically recoverable and reusable catalysts for suzuki C--C cross-coupling reactions. , 2009, Chemistry.
[33] M. Fox,et al. Synthesis, Characterization, and Catalytic Applications of a Palladium-Nanoparticle-Cored Dendrimer , 2003 .
[34] M. Witcomb,et al. Catalytic Activity of Metal Nanoparticles Supported on Nitrogen‐Doped Carbon Spheres , 2010 .
[35] R. Cao,et al. Facile synthesis of palladium nanoparticles with high chemical activity using cucurbit[6]uril as protecting agent. , 2010, Chemical communications.
[36] Fang Niu,et al. Pd nanoparticles in silica hollow spheres with mesoporous walls: a nanoreactor with extremely high activity. , 2010, Chemical communications.
[37] D. Jiang,et al. CMPs as scaffolds for constructing porous catalytic frameworks: a built-in heterogeneous catalyst with high activity and selectivity based on nanoporous metalloporphyrin polymers. , 2010, Journal of the American Chemical Society.
[38] V. Choudhary,et al. Pd–Cu–Exchanged montmorillonite K10 clay: an efficient and reusable heterogeneous catalyst for vinylation of aryl halides , 1997 .
[39] H. Yoshida,et al. Origin of the excellent catalytic activity of Pd loaded on ultra-stable Y zeolites in Suzuki–Miyaura reactions , 2010 .
[40] S. Özkar,et al. Room temperature aerobic Suzuki cross-coupling reactions in DMF/water mixture using zeolite confined palladium(0) nanoclusters as efficient and recyclable catalyst , 2010 .
[41] Mostafa A. El-Sayed,et al. Size effects of PVP-Pd nanoparticles on the catalytic Suzuki reactions in aqueous solution , 2002 .
[42] Adria R. Wilson,et al. Synthesis and catalytic properties of Au-Pd nanoflowers. , 2011, ACS nano.
[43] A. Biffis,et al. Palladium metal catalysts in Heck CC coupling reactions , 2001 .
[44] Zhancheng Ma,et al. Mesoporous Ethane−Silicas Functionalized with a Bulky N-Heterocyclic Carbene for Suzuki−Miyaura Coupling of Aryl Chlorides and Benzyl Chlorides , 2010 .
[45] L. Wan,et al. An Efficient and Recyclable Fluorous Palladium Catalyst for the Room-Temperature Suzuki Reaction , 2011 .
[46] K. Ebert,et al. Nanofiltration for Homogeneous Catalysis Separation: Soluble Polymer-Supported Palladium Catalysts for Heck, Sonogashira, and Suzuki Coupling of Aryl Halides , 2003 .
[47] R. Varma,et al. The synthesis and applications of a micro-pine-structured nanocatalyst. , 2008, Chemical communications.
[48] Wangqing Zhang,et al. Pd Nanoparticles Immobilized on pH-Responsive and Chelating Nanospheres as an Efficient and Recyclable Catalyst for Suzuki Reaction in Water , 2008 .
[49] Jia Guo,et al. Solution-Dispersible, Colloidal, Conjugated Porous Polymer Networks with Entrapped Palladium Nanocrystals for Heterogeneous Catalysis of the Suzuki–Miyaura Coupling Reaction , 2011 .
[50] Zhiyong Wang,et al. Diatomite-supported Pd nanoparticles: an efficient catalyst for Heck and Suzuki reactions. , 2006, The Journal of organic chemistry.
[51] M. Witcomb,et al. In-situ synthesis of a palladium-polyaniline hybrid catalyst for a Suzuki coupling reaction , 2011 .
[52] S. Waghmode,et al. Studies on Pd/NiFe2O4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls , 2011, Beilstein journal of organic chemistry.
[53] Jun Hu,et al. Pd nanoparticle aging and its implications in the suzuki cross-coupling reaction. , 2005, Langmuir : the ACS journal of surfaces and colloids.
[54] Steven V Ley,et al. Polyurea-encapsulated palladium(II) acetate: a robust and recyclable catalyst for use in conventional and supercritical media. , 2002, Chemical communications.
[55] A. Pombeiro,et al. Single-pot template transformations of cyanopyridines on a Pd(II) centre: syntheses of ketoimine and 2,4-dipyridyl-1,3,5-triazapentadiene palladium(II) complexes and their catalytic activity for microwave-assisted Suzuki-Miyaura and Heck reactions. , 2009, Dalton transactions.