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Volumn 36, Issue 8, 2003, Pages 638-643

Formation of carbon-carbon bonds under catalysis by transition-metal nanoparticles

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; COBALT; METAL; PALLADIUM;

EID: 0042975158     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar020267y     Document Type: Article
Times cited : (614)

References (80)
  • 1
    • 0037911022 scopus 로고
    • Chemical catalysis by colloids and clusters
    • Lewis, L. N. Chemical Catalysis by Colloids and Clusters. Chem. Rev. 1993, 93, 2693-2730.
    • (1993) Chem. Rev. , vol.93 , pp. 2693-2730
    • Lewis, L.N.1
  • 2
    • 84955168436 scopus 로고
    • The chemistry of transition metal colloids
    • Schmid, G., Ed.; VCH: Weinheim, Germany
    • Bradley, J. S. The Chemistry of Transition Metal Colloids. In Clusters and Colloids, From Theory to Applications; Schmid, G., Ed.; VCH: Weinheim, Germany, 1994; pp 459-544.
    • (1994) Clusters and Colloids, from Theory to Applications , pp. 459-544
    • Bradley, J.S.1
  • 3
    • 0003898591 scopus 로고    scopus 로고
    • Braunstein, P.; Oro, L., Raithby, P R., Eds.; Wiley-VCH: Weinheim, Germany
    • In Metal Clusters in Chemistry; Braunstein, P.; Oro, L., Raithby, P R., Eds.; Wiley-VCH: Weinheim, Germany, 1998.
    • (1998) Metal Clusters in Chemistry
  • 5
    • 0002486241 scopus 로고    scopus 로고
    • Nanoparticles and nanostructural materials
    • Interrante, L. V., Hampden-Smith, M. J., Eds.; Wiley-VCH: New York; Chapter 7
    • Klabunde, K. J.; Mohs, C. Nanoparticles and Nanostructural Materials. In Chemistry of Advanced Materials. An Overview; Interrante, L. V., Hampden-Smith, M. J., Eds.; Wiley-VCH: New York, 1998; Chapter 7, pp 271-327.
    • (1998) Chemistry of Advanced Materials. An Overview , pp. 271-327
    • Klabunde, K.J.1    Mohs, C.2
  • 6
    • 0033536428 scopus 로고    scopus 로고
    • A review of modern transition-metal nanoclusters their synthesis, characterization, and applications in catalysis
    • Aiken III, J. D.; Finke, R. G. A Review of Modern Transition-Metal Nanoclusters: Their Synthesis, Characterization, and Applications in Catalysis. J. Mol. Catal. A 1999, 145, 1-44.
    • (1999) J. Mol. Catal. A , vol.145 , pp. 1-44
    • Aiken J.D. III1    Finke, R.G.2
  • 8
    • 0035803697 scopus 로고    scopus 로고
    • Organic nanoparticles in the aqueous phase - Theory, experiment, and use
    • Horn, D.; Rieger, J. Organic Nanoparticles in the Aqueous Phase - Theory, Experiment, and Use. Angew. Chem., Int. Ed. Engl. 2001, 40, 4330-4361.
    • (2001) Angew. Chem., Int. Ed. Engl. , vol.40 , pp. 4330-4361
    • Horn, D.1    Rieger, J.2
  • 9
    • 0035793822 scopus 로고    scopus 로고
    • Size-selective electrochemical preparation of surfactant-stabilized Pd-. Ni- and Pt/Pd colloids
    • Reetz, M. T.; Winter, M.; Breinbauer, R.; Thurn-Albrecht, T.; Vogel, W. Size-Selective Electrochemical Preparation of Surfactant-Stabilized Pd-. Ni- and Pt/Pd Colloids. Chem. Eur. J. 2001, 7, 1084-1094.
    • (2001) Chem. Eur. J. , vol.7 , pp. 1084-1094
    • Reetz, M.T.1    Winter, M.2    Breinbauer, R.3    Thurn-Albrecht, T.4    Vogel, W.5
  • 10
    • 0035131970 scopus 로고    scopus 로고
    • Nanoengineering of particle surfaces
    • Caruso, F. Nanoengineering of Particle Surfaces. Adv. Mater. 2001, 13, 11-22.
    • (2001) Adv. Mater. , vol.13 , pp. 11-22
    • Caruso, F.1
  • 11
    • 0034784439 scopus 로고    scopus 로고
    • Nanoscopic metal particles synthetic methods and potential applications
    • Bönnemann, H.; Richards, R. M. Nanoscopic Metal Particles Synthetic Methods and Potential Applications. Eur. J. Inorg. Chem. 2001, 2455-2480,
    • (2001) Eur. J. Inorg. Chem. , pp. 2455-2480
    • Bönnemann, H.1    Richards, R.M.2
  • 14
    • 0036811253 scopus 로고    scopus 로고
    • Reduced transition metal colloids: A novel family of reusable catalysts?
    • Roucoux, A.; Schulz, J.; Patin, H. Reduced Transition Metal Colloids: A Novel Family of Reusable Catalysts? Chem. Rev. 2002, 102, 3757-3778.
    • (2002) Chem. Rev. , vol.102 , pp. 3757-3778
    • Roucoux, A.1    Schulz, J.2    Patin, H.3
  • 16
    • 24844469518 scopus 로고    scopus 로고
    • Fluorous nanoparticles
    • Gladysz, J. A., Curran, D. P., Horváth, I. T., Eds.; Wiley-VCH: in press
    • Moreno-Mañas, M.; Pleixats, R. Fluorous Nanoparticles. In Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horváth, I. T., Eds.; Wiley-VCH: in press.
    • Handbook of Fluorous Chemistry
    • Moreno-Mañas, M.1    Pleixats, R.2
  • 17
    • 0003995267 scopus 로고    scopus 로고
    • Negishi, E., Ed.; Wiley-Interscience: New York
    • For a comprehensive book on palladium in organic chemistry, see: In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley-Interscience: New York, 2002.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis
  • 18
    • 0032335204 scopus 로고    scopus 로고
    • Variations on a theme - Recent developments on the mechanism of the heck reaction and their implications for synthesis
    • For most recent reviews see: (a) Crisp, G. T. Variations on a Theme - Recent Developments on the Mechanism of the Heck Reaction and Their Implications for Synthesis. Chem. Soc. Rev. 1998, 27, 427-436. (b) Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100, 3009-3066. (c) Whitcombe, N. J.; Hii, K. K.; Gibson, S. E. Advances in the Heck Chemistry of Aryl Bromides and Chlorides. Tetrahedron 2001, 57, 7449-7476. (d) Bhanage, B. M.; Arai, M. Catalyst Product Separation Techniques in Heck Reaction. Catal. Rev. 2001, 43, 315-344.
    • (1998) Chem. Soc. Rev. , vol.27 , pp. 427-436
    • Crisp, G.T.1
  • 19
    • 0034249671 scopus 로고    scopus 로고
    • The heck reaction as a sharpening stone of palladium catalysis
    • For most recent reviews see: (a) Crisp, G. T. Variations on a Theme - Recent Developments on the Mechanism of the Heck Reaction and Their Implications for Synthesis. Chem. Soc. Rev. 1998, 27, 427-436. (b) Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100, 3009-3066. (c) Whitcombe, N. J.; Hii, K. K.; Gibson, S. E. Advances in the Heck Chemistry of Aryl Bromides and Chlorides. Tetrahedron 2001, 57, 7449-7476. (d) Bhanage, B. M.; Arai, M. Catalyst Product Separation Techniques in Heck Reaction. Catal. Rev. 2001, 43, 315-344.
    • (2000) Chem. Rev. , vol.100 , pp. 3009-3066
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 20
    • 0035959456 scopus 로고    scopus 로고
    • Advances in the heck chemistry of aryl bromides and chlorides
    • For most recent reviews see: (a) Crisp, G. T. Variations on a Theme - Recent Developments on the Mechanism of the Heck Reaction and Their Implications for Synthesis. Chem. Soc. Rev. 1998, 27, 427-436. (b) Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100, 3009-3066. (c) Whitcombe, N. J.; Hii, K. K.; Gibson, S. E. Advances in the Heck Chemistry of Aryl Bromides and Chlorides. Tetrahedron 2001, 57, 7449-7476. (d) Bhanage, B. M.; Arai, M. Catalyst Product Separation Techniques in Heck Reaction. Catal. Rev. 2001, 43, 315-344.
    • (2001) Tetrahedron , vol.57 , pp. 7449-7476
    • Whitcombe, N.J.1    Hii, K.K.2    Gibson, S.E.3
  • 21
    • 0035414104 scopus 로고    scopus 로고
    • Catalyst product separation techniques in heck reaction
    • For most recent reviews see: (a) Crisp, G. T. Variations on a Theme - Recent Developments on the Mechanism of the Heck Reaction and Their Implications for Synthesis. Chem. Soc. Rev. 1998, 27, 427-436. (b) Beletskaya, I. P.; Cheprakov, A. V. The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem. Rev. 2000, 100, 3009-3066. (c) Whitcombe, N. J.; Hii, K. K.; Gibson, S. E. Advances in the Heck Chemistry of Aryl Bromides and Chlorides. Tetrahedron 2001, 57, 7449-7476. (d) Bhanage, B. M.; Arai, M. Catalyst Product Separation Techniques in Heck Reaction. Catal. Rev. 2001, 43, 315-344.
    • (2001) Catal. Rev. , vol.43 , pp. 315-344
    • Bhanage, B.M.1    Arai, M.2
  • 22
    • 0030600195 scopus 로고    scopus 로고
    • Suzuki and heck reactions catalyzed by preformed palladium clusters and palladium/nickel bimetallic clusters
    • Reetz, M. T.; Breinbauer, R.; Wanninger, K. Suzuki and Heck Reactions Catalyzed by Preformed Palladium Clusters and Palladium/Nickel Bimetallic Clusters. Tetrahedron Lett. 1996, 37, 4499-4502.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4499-4502
    • Reetz, M.T.1    Breinbauer, R.2    Wanninger, K.3
  • 23
    • 0000184683 scopus 로고    scopus 로고
    • Propylene carbonate stabilized nanostructured palladium clusters as catalysts in heck reactions
    • Reetz, M. T.; Lohmer, G. Propylene Carbonate Stabilized Nanostructured Palladium Clusters as Catalysts in Heck Reactions. Chem. Commun. 1996, 1921-1922.
    • (1996) Chem. Commun. , pp. 1921-1922
    • Reetz, M.T.1    Lohmer, G.2
  • 24
    • 0034598519 scopus 로고    scopus 로고
    • Phosphane-free palladium-catalyzed coupling reactions: The decisive role of Pd nanoparticles
    • Reetz, M. T.; Westermann, E. Phosphane-Free Palladium-Catalyzed Coupling Reactions: The Decisive Role of Pd Nanoparticles. Angew. Chem., Int. Ed. Engl. 2000, 39, 165-168.
    • (2000) Angew. Chem., Int. Ed. Engl. , vol.39 , pp. 165-168
    • Reetz, M.T.1    Westermann, E.2
  • 25
    • 0030598098 scopus 로고    scopus 로고
    • On the efficiency of tetraalkylammonium salts in heck type reactions
    • Jeffery, T. On the Efficiency of Tetraalkylammonium Salts in Heck Type Reactions. Tetrahedron 1996, 52, 10113-10130.
    • (1996) Tetrahedron , vol.52 , pp. 10113-10130
    • Jeffery, T.1
  • 26
  • 27
    • 0030694572 scopus 로고    scopus 로고
    • Preparation of palladium colloids in block copolymer micelles and their use for the catalysis of the heck reaction
    • Klingelhöfer, S.; Heitz, W.; Greiner, A.; Oestreich, S.; Förster, S.; Antonietti, M. Preparation of Palladium Colloids in Block Copolymer Micelles and Their use for the Catalysis of the Heck Reaction. J. Am. Chem. Soc. 1997, 119, 10116-10120.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 10116-10120
    • Klingelhöfer, S.1    Heitz, W.2    Greiner, A.3    Oestreich, S.4    Förster, S.5    Antonietti, M.6
  • 28
    • 0000780927 scopus 로고    scopus 로고
    • Sonochemical preparation and properties of nanostructured palladium metallic clusters
    • Dhas, N. A.; Gedanken, A. Sonochemical Preparation and Properties of Nanostructured Palladium Metallic Clusters. J. Mater. Chem. 1998, 8, 445-450.
    • (1998) J. Mater. Chem. , vol.8 , pp. 445-450
    • Dhas, N.A.1    Gedanken, A.2
  • 29
    • 0342264731 scopus 로고    scopus 로고
    • Hexagonal or quasi two-dimensional palladium nanoparticles - Tested at the heck reaction
    • Walter, J.; Heiermann, J.; Dyker, G.; Hara, S.; Shioyama, H. Hexagonal or Quasi Two-Dimensional Palladium Nanoparticles - Tested at the Heck Reaction. J. Catal. 2000, 189, 449-455.
    • (2000) J. Catal. , vol.189 , pp. 449-455
    • Walter, J.1    Heiermann, J.2    Dyker, G.3    Hara, S.4    Shioyama, H.5
  • 31
    • 0034599063 scopus 로고    scopus 로고
    • Heck reactions of iodobenzene and methyl acrylate with conventional supported palladium catalysts in the presence or organic and/or inorganic bases without ligands
    • Zhao, F.; Bhanage, B. M.; Shirai, M.; Arai, M. Heck Reactions of Iodobenzene and Methyl Acrylate with Conventional Supported Palladium Catalysts in the Presence or Organic and/or Inorganic Bases without Ligands. Chem. Eur. J. 2000, 6, 843-848.
    • (2000) Chem. Eur. J. , vol.6 , pp. 843-848
    • Zhao, F.1    Bhanage, B.M.2    Shirai, M.3    Arai, M.4
  • 32
    • 0032676940 scopus 로고    scopus 로고
    • Catalytically active Pd(0) nanocomposites based on a liquid crystal template
    • (a) Ding, J. A.; Gin, D. L. Catalytically Active Pd(0) Nanocomposites Based on a Liquid Crystal Template. Polymer Preprints 1999, 40, 738-739.
    • (1999) Polymer Preprints , vol.40 , pp. 738-739
    • Ding, J.A.1    Gin, D.L.2
  • 33
    • 0033803215 scopus 로고    scopus 로고
    • Catalytic Pd nanoparticles synthesized using a lyotropic liquid crystal polymer template
    • (b) Ding, J. H.; Gin, D. L. Catalytic Pd Nanoparticles Synthesized Using a Lyotropic Liquid Crystal Polymer Template. Chem. Mater. 2000, 12, 22-24.
    • (2000) Chem. Mater. , vol.12 , pp. 22-24
    • Ding, J.H.1    Gin, D.L.2
  • 34
    • 0035823344 scopus 로고    scopus 로고
    • Ultrasound promoted C-C bond formation: Heck reaction at ambient conditions in room-temperature ionic liquids
    • Deshmukh, R. R.; Rajagopat, R.; Srinivasan, K. V. Ultrasound Promoted C-C Bond Formation: Heck Reaction at Ambient Conditions in Room-Temperature Ionic Liquids. Chem. Commun. 2001, 1544-1545.
    • (2001) Chem. Commun. , pp. 1544-1545
    • Deshmukh, R.R.1    Rajagopat, R.2    Srinivasan, K.V.3
  • 35
    • 0037010004 scopus 로고    scopus 로고
    • Controlled synthesis of hydroxyapatite-supported palladium complexes as highly efficient heterogeneous catalysts
    • Mori, K.; Yamaguchi, K.; Hara, T.; Mizugaki, T.; Ebitani, K.; Kaneda, K. Controlled Synthesis of Hydroxyapatite-Supported Palladium Complexes as Highly Efficient Heterogeneous Catalysts. J. Am. Chem. Soc. 2002, 124, 11572-11573.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11572-11573
    • Mori, K.1    Yamaguchi, K.2    Hara, T.3    Mizugaki, T.4    Ebitani, K.5    Kaneda, K.6
  • 36
    • 0012718418 scopus 로고    scopus 로고
    • Carbon carbon and carbon - Nitrogen coupling reactions catalyzed by palladium nanoparticles derived from a palladium substituted keggin-type polyoxometalate
    • Kogan, V.; Aizenshtat, Z.; Popovitz-Biro, R.; Neumann, R. Carbon Carbon and Carbon - Nitrogen Coupling Reactions Catalyzed by Palladium Nanoparticles Derived from a Palladium Substituted Keggin-Type Polyoxometalate. Org. Lett. 2002, 4, 3529-3532.
    • (2002) Org. Lett. , vol.4 , pp. 3529-3532
    • Kogan, V.1    Aizenshtat, Z.2    Popovitz-Biro, R.3    Neumann, R.4
  • 37
    • 0037149353 scopus 로고    scopus 로고
    • A new bifunctional catalyst for tandem heck-asymmetric dihydroxylation of olefins
    • Choudary, B. M.; Chowdari, N. S.; Jyothi, K.; Kumar, N. S.; Kantam, M. L. A New Bifunctional Catalyst for Tandem Heck-Asymmetric Dihydroxylation of Olefins. Chem. Commun. 2002, 586-587.
    • (2002) Chem. Commun. , pp. 586-587
    • Choudary, B.M.1    Chowdari, N.S.2    Jyothi, K.3    Kumar, N.S.4    Kantam, M.L.5
  • 38
    • 0037161779 scopus 로고    scopus 로고
    • Highly reactive heterogeneous heck and hydrogenation catalysts constructed through "bottom-up" nanoparticle self-assembly
    • Galow, T. H.; Drechsler, U.; Hanson, J. A.; Rotello, V. M. Highly Reactive Heterogeneous Heck and Hydrogenation Catalysts Constructed through "Bottom-up" Nanoparticle Self-Assembly. Chem. Commun. 2002, 1076-1077.
    • (2002) Chem. Commun. , pp. 1076-1077
    • Galow, T.H.1    Drechsler, U.2    Hanson, J.A.3    Rotello, V.M.4
  • 39
    • 0037184451 scopus 로고    scopus 로고
    • Layered double hydroxide supported nanopalladium catalyst for heck-, Suzuki-, Sonogashira-, and Stille-type coupling reactions of chloroarenes
    • Choudary, B. M.; Madhi, S.; Chowdari, N. S.; Kantam, M. L.; Sreedhar, B. Layered Double Hydroxide Supported Nanopalladium Catalyst for Heck-, Suzuki-, Sonogashira-, and Stille-Type Coupling Reactions of Chloroarenes, J. Am. Chem. Soc. 2002, 124, 14127-14136.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 14127-14136
    • Choudary, B.M.1    Madhi, S.2    Chowdari, N.S.3    Kantam, M.L.4    Sreedhar, B.5
  • 40
    • 0037460170 scopus 로고    scopus 로고
    • A modular approach toward functionalized three-dimensional macromolecules from synthetic concepts to practical applications
    • Bosman, A. W.; Vestberg, R.; Heumann, A.; Fréchet, J. M. J.; Hawker, C. J. A Modular Approach toward Functionalized Three-Dimensional Macromolecules: From Synthetic Concepts to Practical Applications. J. Am. Chem. Soc. 2003, 125, 715-728.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 715-728
    • Bosman, A.W.1    Vestberg, R.2    Heumann, A.3    Fréchet, J.M.J.4    Hawker, C.J.5
  • 41
    • 0000736026 scopus 로고    scopus 로고
    • In situ preparation of amorphous carbon-activated palladium nanoparticles
    • Dhas, N. A.; Cohen, H.; Gedanken, A. In Situ Preparation of Amorphous Carbon-Activated Palladium Nanoparticles. J. Phys. Chem. B 1997, 101, 6834-6838.
    • (1997) J. Phys. Chem. B , vol.101 , pp. 6834-6838
    • Dhas, N.A.1    Cohen, H.2    Gedanken, A.3
  • 42
    • 0033320299 scopus 로고    scopus 로고
    • A catalytic probe of the surface of colloidal palladium particles using heck coupling reactions
    • Le Bars, J.; Specht, U.; Bradley, J. S.; Blackmond, D. G. A Catalytic Probe of the Surface of Colloidal Palladium Particles Using Heck Coupling Reactions. Langmuir 1999, 15, 7621-7625.
    • (1999) Langmuir , vol.15 , pp. 7621-7625
    • Le Bars, J.1    Specht, U.2    Bradley, J.S.3    Blackmond, D.G.4
  • 43
    • 0002737158 scopus 로고    scopus 로고
    • Heck heterocoupling within a dendritic nanoreactor
    • Yeung, L. K.; Crooks, R. M. Heck Heterocoupling within a Dendritic Nanoreactor. Nanoletters 2001, 1, 14-17.
    • (2001) Nanoletters , vol.1 , pp. 14-17
    • Yeung, L.K.1    Crooks, R.M.2
  • 44
    • 0034867043 scopus 로고    scopus 로고
    • Dendrimer-encapsulated metal nanoparticles: Synthesis, characterization, and applications in catalysis
    • For reviews on catalysis by nanoparticles by Crooks group see: (a) Crooks, R. M.; Zhao, M.; Sun, L.; Chechik, V.; Yeung, L. K. Dendrimer-Encapsulated Metal Nanoparticles: Synthesis, Characterization, and Applications in Catalysis. Acc. Chem. Res. 2001, 34, 181-190. (b) Crooks, R. M. ; Lemon, B. I., III; Sun, L.; Yeung, L. K.; Zhao, M. Dendrimer-Encapsulated Metals and Semiconductors: Synthesis, Characterization, and Applications. Top. Curr. Chem. 2001, 212, 81-135.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 181-190
    • Crooks, R.M.1    Zhao, M.2    Sun, L.3    Chechik, V.4    Yeung, L.K.5
  • 45
    • 0034867043 scopus 로고    scopus 로고
    • Dendrimer-encapsulated metals and semiconductors: Synthesis, characterization, and applications
    • For reviews on catalysis by nanoparticles by Crooks group see: (a) Crooks, R. M.; Zhao, M.; Sun, L.; Chechik, V.; Yeung, L. K. Dendrimer-Encapsulated Metal Nanoparticles: Synthesis, Characterization, and Applications in Catalysis. Acc. Chem. Res. 2001, 34, 181-190. (b) Crooks, R. M. ; Lemon, B. I., III; Sun, L.; Yeung, L. K.; Zhao, M. Dendrimer-Encapsulated Metals and Semiconductors: Synthesis, Characterization, and Applications. Top. Curr. Chem. 2001, 212, 81-135.
    • (2001) Top. Curr. Chem. , vol.212 , pp. 81-135
    • Crooks, R.M.1    Lemon B.I. III2    Sun, L.3    Yeung, L.K.4    Zhao, M.5
  • 47
    • 0001150340 scopus 로고    scopus 로고
    • Heck reactions catalyzed by PAMAM-dendrimer encapsulated Pd(0) nanoparticles
    • Rahim, E. H.; Kamounah, F. S.; Frederiksen, J.; Christensen, J. B. Heck Reactions Catalyzed by PAMAM-Dendrimer Encapsulated Pd(0) Nanoparticles. Nanoletters 2001, 1, 499-501.
    • (2001) Nanoletters , vol.1 , pp. 499-501
    • Rahim, E.H.1    Kamounah, F.S.2    Frederiksen, J.3    Christensen, J.B.4
  • 48
    • 0035969272 scopus 로고    scopus 로고
    • Fluorous phase soluble palladium nanoparticles as recoverable catalysts for Suzuki cross-coupling and heck reactions
    • Moreno-Mañas, M., Pleixats, R.; Villarroya, S. Fluorous Phase Soluble Palladium Nanoparticles as Recoverable Catalysts for Suzuki Cross-Coupling and Heck Reactions. Organometallics 2001, 20, 4524-4528.
    • (2001) Organometallics , vol.20 , pp. 4524-4528
    • Moreno-Mañas, M.1    Pleixats, R.2    Villarroya, S.3
  • 49
    • 0001489150 scopus 로고    scopus 로고
    • Highly active thermomorphic fluorous palladacycle catalyst precursors for the heck reaction; Evidence for a palladium nanoparticle pathway
    • Rocaboy, C.; Gladysz, J. A. Highly Active Thermomorphic Fluorous Palladacycle Catalyst Precursors for the Heck Reaction; Evidence for a Palladium Nanoparticle Pathway. Org. Lett. 2002, 4, 1993-1996.
    • (2002) Org. Lett. , vol.4 , pp. 1993-1996
    • Rocaboy, C.1    Gladysz, J.A.2
  • 50
    • 0037241661 scopus 로고    scopus 로고
    • Thermomorphic fluorous imine and thioether palladacycles as precursors for highly active heck and Suzuki catalysts; evidence for palladium nanoparticle pathways
    • Rocaboy, C.; Gladysz, J. A. Thermomorphic Fluorous Imine and Thioether Palladacycles as Precursors for Highly Active Heck and Suzuki Catalysts; Evidence for Palladium Nanoparticle Pathways. New J. Chem. 2003, 27, 39-49,
    • (2003) New J. Chem. , vol.27 , pp. 39-49
    • Rocaboy, C.1    Gladysz, J.A.2
  • 51
    • 0346786657 scopus 로고    scopus 로고
    • Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998
    • For recent reviews on the Suzuki coupling see: (a) Suzuki, A. Recent Advances in the Cross-Coupling Reactions of Organoboron Derivatives with Organic Electrophiles, 1995-1998. J. Organomet. Chem. 1999, 576, 147-168. (b) Kotha, S.; Lahiri, K.; Kashinath, D. Tetrahedron 2002, 58, 9633-9695.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 147-168
    • Suzuki, A.1
  • 52
    • 0037175592 scopus 로고    scopus 로고
    • For recent reviews on the Suzuki coupling see: (a) Suzuki, A. Recent Advances in the Cross-Coupling Reactions of Organoboron Derivatives with Organic Electrophiles, 1995-1998. J. Organomet. Chem. 1999, 576, 147-168. (b) Kotha, S.; Lahiri, K.; Kashinath, D. Tetrahedron 2002, 58, 9633-9695.
    • (2002) Tetrahedron , vol.58 , pp. 9633-9695
    • Kotha, S.1    Lahiri, K.2    Kashinath, D.3
  • 53
    • 0000934066 scopus 로고    scopus 로고
    • Suzuki cross-coupling reactions catalyzed by palladium nanoparticles in aqueous solution
    • Li, Y.; Hong, X. M.; Collard, D. M.; El-Sayed, M. A. Suzuki Cross-Coupling Reactions Catalyzed by Palladium Nanoparticles in Aqueous Solution. Org. Lett. 2000, 2, 2385-2388.
    • (2000) Org. Lett. , vol.2 , pp. 2385-2388
    • Li, Y.1    Hong, X.M.2    Collard, D.M.3    El-Sayed, M.A.4
  • 54
    • 0035922532 scopus 로고    scopus 로고
    • The effect of stabilizers on the catalytic activity of pd colloidal nanoparticles in the Suzuki reactions in aqueous solution
    • Li, Y.; El-Sayed, M. A. The Effect of Stabilizers on the Catalytic Activity of Pd Colloidal Nanoparticles in the Suzuki Reactions in Aqueous Solution. J. Phys. Chem. B 2001, 105, 8938-8943.
    • (2001) J. Phys. Chem. B , vol.105 , pp. 8938-8943
    • Li, Y.1    El-Sayed, M.A.2
  • 55
    • 0037062796 scopus 로고    scopus 로고
    • Size effects of PVP-Pd nanoparticles on the catalytic Suzuki reactions in aqueous solution
    • Li, Y.; Boone, E.; El-Sayed, M. A. Size Effects of PVP-Pd Nanoparticles on the Catalytic Suzuki Reactions in Aqueous Solution. Langmuir 2002, 18, 4921-4925.
    • (2002) Langmuir , vol.18 , pp. 4921-4925
    • Li, Y.1    Boone, E.2    El-Sayed, M.A.3
  • 57
    • 0037014677 scopus 로고    scopus 로고
    • Fabrication of hollow palladium spheres and their successful applications to the recyclable heterogeneous catalyst for Suzuki coupling reactions
    • Kim, S.-W-; Kim, M.; Lee, W. Y.; Hyeon, T. Fabrication of Hollow Palladium Spheres and Their Successful Applications to the Recyclable Heterogeneous Catalyst for Suzuki Coupling Reactions. J. Am. Chem. Soc. 2002, 124, 7642-7643.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 7642-7643
    • Kim, S.W.1    Kim, M.2    Lee, W.Y.3    Hyeon, T.4
  • 58
    • 0037457921 scopus 로고    scopus 로고
    • Cyclodextrin-capped palladium nanoparticles as catalysts for the Suzuki reaction
    • Strimbu, L.; Liu, J.; Kaifer, A. E. Cyclodextrin-Capped Palladium Nanoparticles as Catalysts for the Suzuki Reaction. Langmuir 2003, 19, 483-485.
    • (2003) Langmuir , vol.19 , pp. 483-485
    • Strimbu, L.1    Liu, J.2    Kaifer, A.E.3
  • 59
    • 0037071245 scopus 로고    scopus 로고
    • Synthesis, oxidations, and palladium complexes of fluorous dialkyl sulfides: New precursors to highly active catalysts for the suzuki coupling
    • Rocaboy, C.; Gladysz, J. A. Synthesis, Oxidations, and Palladium Complexes of Fluorous Dialkyl Sulfides: New Precursors to Highly Active Catalysts for the Suzuki Coupling. Tetrahedron 2002, 58, 4007-4014.
    • (2002) Tetrahedron , vol.58 , pp. 4007-4014
    • Rocaboy, C.1    Gladysz, J.A.2
  • 60
    • 0033536264 scopus 로고    scopus 로고
    • Palladium catalyzed hydroxycarbonylation of olefins in biphasic system: Beneficial effect of alkali metal salt and protective-colloid agents on the stability of the catalytic system
    • Bertoux, F.; Monflier, E.; Castanet, Y.; Mortreux, A. Palladium Catalyzed Hydroxycarbonylation of Olefins in Biphasic system: Beneficial Effect of Alkali Metal Salt and Protective-Colloid Agents on the Stability of the Catalytic System. J. Mol. Catal. A 1999, 143, 23-30.
    • (1999) J. Mol. Catal. A , vol.143 , pp. 23-30
    • Bertoux, F.1    Monflier, E.2    Castanet, Y.3    Mortreux, A.4
  • 61
    • 0034685862 scopus 로고    scopus 로고
    • Tandem one-pot palladium-catalyzed reductive and oxidative coupling of benzene and chlorobenzene
    • Mukhopadhyay, S.; Rothenberg, G.; Gitis, D.; Sasson, Y. Tandem One-Pot Palladium-Catalyzed Reductive and Oxidative Coupling of Benzene and Chlorobenzene. J. Org. Chem. 2000, 65, 3107-3110.
    • (2000) J. Org. Chem. , vol.65 , pp. 3107-3110
    • Mukhopadhyay, S.1    Rothenberg, G.2    Gitis, D.3    Sasson, Y.4
  • 63
    • 0000939078 scopus 로고    scopus 로고
    • Transition metal alkyne complexes: The pauson-khand reaction
    • For recent reviews on the Pauson-Khand reaction see: (a) Chung, Y. K. Transition Metal Alkyne Complexes: the Pauson-Khand Reaction. Coord. Chem. Rev. 1999, 188, 297-341. (b) Fletcher, A. J.; Christie, S. D. R. J. Chem. Soc., Perkin Trans. 1 2000, 1657-1668.
    • (1999) Coord. Chem. Rev. , vol.188 , pp. 297-341
    • Chung, Y.K.1
  • 64
    • 0034616733 scopus 로고    scopus 로고
    • For recent reviews on the Pauson-Khand reaction see: (a) Chung, Y. K. Transition Metal Alkyne Complexes: the Pauson-Khand Reaction. Coord. Chem. Rev. 1999, 188, 297-341. (b) Fletcher, A. J.; Christie, S. D. R. J. Chem. Soc., Perkin Trans. 1 2000, 1657-1668.
    • (2000) J. Chem. Soc., Perkin Trans. 1 , pp. 1657-1668
    • Fletcher, A.J.1    Christie, S.D.R.2
  • 65
    • 0035823936 scopus 로고    scopus 로고
    • Colloidal cobalt nanoparticles: A highly active and reusable pauson-khand catalyst
    • Kim, S.-W.; Son, S. U.; Lee, S. S.; Hyeon, T.; Chung, Y. K. Colloidal Cobalt Nanoparticles: a Highly Active and Reusable Pauson-Khand Catalyst. Chem. Commun. 2001, 2212-2213.
    • (2001) Chem. Commun. , pp. 2212-2213
    • Kim, S.-W.1    Son, S.U.2    Lee, S.S.3    Hyeon, T.4    Chung, Y.K.5
  • 66
    • 0000266263 scopus 로고    scopus 로고
    • The first intramolecular pauson-khand reaction in water using aqueous colloidal cobalt nanoparticles as catalysts
    • Son, S. U.; Lee, S. I.; Chung, Y. K.; Kim, S.-W.; Hyeon, T. The First Intramolecular Pauson-Khand Reaction in Water Using Aqueous Colloidal Cobalt Nanoparticles as Catalysts. Org. Lett. 2002, 4, 277-279.
    • (2002) Org. Lett. , vol.4 , pp. 277-279
    • Son, S.U.1    Lee, S.I.2    Chung, Y.K.3    Kim, S.-W.4    Hyeon, T.5
  • 67
    • 0041533081 scopus 로고    scopus 로고
    • Cobalt nanoparticles on charcoal: A versatile catalyst in the pauson-khand reaction, hydrogenation, and the reductive pauson-khand reaction
    • Son, S. U.; Park, K. H.; Chung, Y. K. Cobalt Nanoparticles on Charcoal: A Versatile Catalyst in the Pauson-Khand Reaction, Hydrogenation, and the Reductive Pauson-Khand Reaction. Org. Lett. 2002, 4, 3983-3986.
    • (2002) Org. Lett. , vol.4 , pp. 3983-3986
    • Son, S.U.1    Park, K.H.2    Chung, Y.K.3
  • 68
    • 0038750448 scopus 로고    scopus 로고
    • Sequential actions of palladium and cobalt nanoparticles immobilized on silica: One-pot synthesis of bicyclic enones by catalytic allylic alkylation and pauson-khand reaction
    • Park, K. H.; Son, S. U.; Chung, Y. K. Sequential Actions of Palladium and Cobalt Nanoparticles Immobilized on Silica: One-Pot Synthesis of Bicyclic Enones by Catalytic Allylic Alkylation and Pauson-Khand Reaction. Org. Lett. 2002, 4, 4361-4363.
    • (2002) Org. Lett. , vol.4 , pp. 4361-4363
    • Park, K.H.1    Son, S.U.2    Chung, Y.K.3
  • 69
    • 0037134803 scopus 로고    scopus 로고
    • Sequential actions of cobalt nanoparticles and palladium(II) catalysts: Three-step one-pot synthesis of fenestranes from an enyne and an alkyne diester
    • Son, S. U.; Park, K. H.; Chung, Y. K. Sequential Actions of Cobalt Nanoparticles and Palladium(II) Catalysts: Three-Step One-Pot Synthesis of Fenestranes from an Enyne and an Alkyne Diester. J. Am. Chem. Soc. 2002, 124, 6838-6839.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6838-6839
    • Son, S.U.1    Park, K.H.2    Chung, Y.K.3
  • 70
    • 0037048713 scopus 로고    scopus 로고
    • Copper-catalyzed Suzuki cross-coupling using mixed nanocluster catalysis
    • Thathagar, M. B.; Beckers, J.; Rothenberg, G. Copper-Catalyzed Suzuki Cross-Coupling Using Mixed Nanocluster Catalysis. J. Am. Chem. Soc. 2002, 124, 11858-11859.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11858-11859
    • Thathagar, M.B.1    Beckers, J.2    Rothenberg, G.3
  • 71
    • 21344463562 scopus 로고    scopus 로고
    • IR characterization of products of acetylene polymerization over Nano-Cu Particles
    • Chen, K.; Zhang, Z.; Cui, Z.; Yang, D. IR Characterization of Products of Acetylene Polymerization over Nano-Cu Particles. Gaofenzi Xuebao 2000, 180-183; Chem, Abstr. 133, 59490.
    • (2000) Gaofenzi Xuebao , pp. 180-183
    • Chen, K.1    Zhang, Z.2    Cui, Z.3    Yang, D.4
  • 72
    • 0042034328 scopus 로고    scopus 로고
    • Chen, K.; Zhang, Z.; Cui, Z.; Yang, D. IR Characterization of Products of Acetylene Polymerization over Nano-Cu Particles. Gaofenzi Xuebao 2000, 180-183; Chem, Abstr. 133, 59490.
    • Chem. Abstr. , vol.133 , pp. 59490
  • 73
    • 0344588808 scopus 로고    scopus 로고
    • Colloid-bound catalyst for ring-opening metathesis polymerization: A combination of homogeneous and heterogeneous properties
    • Bartz, M.; Küther, J.; Seshadri, R.; Tremel, W. Colloid-Bound Catalyst for Ring-Opening Metathesis Polymerization: A Combination of Homogeneous and Heterogeneous Properties. Angew. Chem., Int. Ed. Engl. 1998, 37, 2466-2468.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 2466-2468
    • Bartz, M.1    Küther, J.2    Seshadri, R.3    Tremel, W.4
  • 74
    • 0000036275 scopus 로고    scopus 로고
    • Electrochemical preparation of nanostructured titanium clusters. Characterization and use in McMurry-Type coupling reactions
    • Reetz, M. T.; Quaiser, S. A.; Merk, C. Electrochemical Preparation of Nanostructured Titanium Clusters. Characterization and Use in McMurry-Type Coupling Reactions. Chem. Ber. 1996, 129, 741-743.
    • (1996) Chem. Ber. , vol.129 , pp. 741-743
    • Reetz, M.T.1    Quaiser, S.A.2    Merk, C.3
  • 75
    • 0032510204 scopus 로고    scopus 로고
    • Nanostructured Nickel-Clusters as catalysts in [3+2] cycloaddition reactions
    • Reetz, M. T.; Breinbauer, R.; Wedemann, P.; Binger, P. Nanostructured Nickel-Clusters as Catalysts in [3+2] Cycloaddition Reactions. Tetrahedron 1998, 54, 1233-1240.
    • (1998) Tetrahedron , vol.54 , pp. 1233-1240
    • Reetz, M.T.1    Breinbauer, R.2    Wedemann, P.3    Binger, P.4
  • 76
    • 0030897984 scopus 로고    scopus 로고
    • Carbonylation of methanol catalyzed by polymer-protected rhodium colloid
    • Wang, Q.; Liu, H.; Han, M.; Li, X.; Jiang, D. Carbonylation of Methanol Catalyzed by Polymer-Protected Rhodium Colloid. J. Mol. Catal. A 1997, 118, 145-151.
    • (1997) J. Mol. Catal. A , vol.118 , pp. 145-151
    • Wang, Q.1    Liu, H.2    Han, M.3    Li, X.4    Jiang, D.5
  • 77
    • 0001097992 scopus 로고    scopus 로고
    • Heck reaction in ionic liquids and the in situ identification of N-heterocyclic carbene complexes of palladium
    • Xu, L.; Chen, W.; Xiao, J. Heck Reaction in Ionic Liquids and the in Situ Identification of N-Heterocyclic Carbene Complexes of Palladium. Organometallics 2000, 19, 1123-1127.
    • (2000) Organometallics , vol.19 , pp. 1123-1127
    • Xu, L.1    Chen, W.2    Xiao, J.3
  • 78
    • 0037419139 scopus 로고    scopus 로고
    • Pd nanoparticles catalyzed stereospecific synthesis of β-Aryl cinnamic esters in ionic liquids
    • Caló, V.; Nacci, A.; Monopoli, A.; Laera, S.; Cioffi, N. Pd Nanoparticles Catalyzed Stereospecific Synthesis of β-Aryl Cinnamic Esters in Ionic Liquids. J. Org. Chem. 2003, 68, 2929-2933.
    • (2003) J. Org. Chem. , vol.68 , pp. 2929-2933
    • Caló, V.1    Nacci, A.2    Monopoli, A.3    Laera, S.4    Cioffi, N.5
  • 79
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids. Solvents for synthesis and catalysis
    • For reviews on ionic liquids see: (a) Welton, T. Room-Temperature Ionic Liquids. Solvents for Synthesis and Catalysis. Chem. Rev. 1999, 99, 2071-2083. (b) Earle, M.; Seddon, K. R. Ionic Liquids. Green Solvents for the Future. Pure Appl. Chem. 2000, 72, 1391-1398.
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2083
    • Welton, T.1
  • 80
    • 0034583251 scopus 로고    scopus 로고
    • Ionic liquids. Green solvents for the future
    • For reviews on ionic liquids see: (a) Welton, T. Room-Temperature Ionic Liquids. Solvents for Synthesis and Catalysis. Chem. Rev. 1999, 99, 2071-2083. (b) Earle, M.; Seddon, K. R. Ionic Liquids. Green Solvents for the Future. Pure Appl. Chem. 2000, 72, 1391-1398.
    • (2000) Pure Appl. Chem. , vol.72 , pp. 1391-1398
    • Earle, M.1    Seddon, K.R.2


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