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磁性可回收钯催化剂催化Suzuki反应的研究进展 被引量:2

Progress in Research on Suzuki Reaction over Magnetical Recoverable Palladium(Pd)-Based Catalysts
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摘要 钯催化剂催化卤代芳烃和芳基硼酸生成碳-碳键的Suzuki偶联反应是合成联苯化合物的最重要的途径之一。相比于传统均相钯催化剂的利用率低,污染产品等缺点,磁性钯催化剂易回收,可重复利用,具有工业化应用前景,受到了广泛的关注。综述了近年来无配体磁性钯催化剂、无包裹磁性钯配体催化剂以及以碳、氧化硅、聚合物包裹的具有核壳结构的磁性钯配体催化剂的制备及其催化Szuki偶联反应的研究进展。 The Suzuki cross-coupling reactions catalyzed by palladium catalysts to form the carbon-carbon bonds between aryl halides and aryl boronic acids is one of the most important way of synthesizing biphenyl compound. Compared with the traditional homogeneous catalysts whose disadvantages are low catalyst recycling rate and polluting products, magnetic palladium-based catalysts are easy separable and recycled, which is suitable for industrial application and attracts much greater attention. This paper introduces some latest development process in the preparation of no-ligand magnetic palladium catalysts, palladium-based catalysts supported on no-coated magnetic particles and shell-core structure palladium-based catalysts support on magnetic particles coated by the materials, such as carbons, silica, polymers and their application in Suzuki reactions.
出处 《化学与粘合》 CAS 2012年第1期48-54,共7页 Chemistry and Adhesion
基金 黑龙江省科学院科研基金项目
关键词 磁性 钯催化剂 SUZUKI反应 Magnetic palladium catalysts Suzuki reaction
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参考文献35

  • 1MIYAURA N, YAMADA K, SUZUKI A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1- alkenylboranes with 1-alkenyl or 1-alkynyl halides[J ]. Tetrahe- dron Letters, 1979, 36:3437-3440.
  • 2MIYAUR N,YANAGI T,SUZUKI A. The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases [J].Synthetic Communications,1981,11(7): 513-515.
  • 3MIYAURA N, SUZUKI A. Palladium-catalyzed cross-coupling reactions of organoboron compounds [J].Chemical Reviews, 1995,95(7):2457-2483.
  • 4KOTHA S, LAHIRI K, KASHINATH D. Recent applications of the Suzuki-Miyaura cross-coupling reaction in organic synthesis [J ].Tetrahe-Dron,2002, 58:9633-9695.
  • 5BAUDOIN O, CESARIO M, GUINARD D,et al.Application of the palladium-catalyzed Borylation/Suzuki coupling (BSC) reaction to the synthesis of biologically active biaryl lactams [ J ].The Jour- nal of Organic Chemistry,2002, 67:1199-1207.
  • 6ROBERTO D A, ARSENIA R. Short synthesis of undecylprodi- giosine. A new route to 2,2"-bipyrrolyl-pyrromethene systems [J]. Synlett,1996,3:513-514.
  • 7CORMA A,DAS D, GARCIA H,et al.A periodic mesoporous organosilica containing a carbapalladacycle complex as heteroge- neous catalyst for Suzuki cross-coupling[J].Journal of Catalysis , 2005, 229:322-331.
  • 8SEKI M.Recent advances in Pd/C-catalyzed coupling reactions [ J ].Synthesis,2006:2975-2992.
  • 9LUO F T,XUE C,KO S L, et al.Preparation of polystyrene-sup- ported soluble palladacycle catalyst for Heck and Suzuki reac- tions [J].Tetrahedron, 2005, 61: 6040-6045.
  • 10POLSHETI'IWAR V, LUQUE R, FIHRI A, et al. Magnetically recoverable nanocatalysts [J]. Chemical Reviews, 2011,111 (5): 3021-3666.

二级参考文献14

  • 1赵晓伟,崔元臣,张纪伟.微波辅助的聚氯乙烯-三乙撑四胺负载钯配合物对Suzuki反应的催化性能[J].有机化学,2007,27(5):597-601. 被引量:2
  • 2Suzuki, A. Chem. Rev. 1995, 95, 2457.
  • 3Wang, Z.; Shen, B.; Zou, A.; He, N. Chem. Eng. J. 2005, 113, 27.
  • 4Wang, Z.; Xiao, P.; Shen, B.; He, N. Colloid. Surf A: Phys. 2006, 276, 16.
  • 5Stevens, P. D.; Fan, J.; Gardimalla, H. M.; Yen, R.; Gao, M. Y. Org. Left. 2005, 7, 2085.
  • 6Zheng, Y.; Stevens, P. D.; Gao, Y. J. Org. Chem. 2006, 71, 537.
  • 7Zhu, Y.; Peng, S. C.; Emi, A.; Su, Z.; Monalisa; Kempd, R. A. Adv. Synth. Catal. 2007, 349, 1917.
  • 8Caruntu, D.; Caruntu, G.; Chen, Y.; O'Connor, C. J.; Goloverda, G.; Kolesnichenko, V. L. Chem. Mater. 2004, 16(25), 5527.
  • 9(olivet, J.-P.; Chaneac, C.; Tronc, E. Chem. Commun. 2004, 481.
  • 10Kang, Y. S.; Risbud, S.; Rabolt, J.; Stroeve, F. P. Chem. Mater. 1996, 8, 2209.

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同被引文献18

  • 1WOLFER J P, SINGER R A, YANG B H, et al. Highly active palladium catalysts for suzuki coupling reactions[J]. Journal of the American Chemical Society, 1999,121 (41) : 9550-9561.
  • 2BEI Xiao-hong, TURNER H W,WEINBERG W H, et al. Palladium/P, O-ligand-catalyzed suzuki cross-coupling re- actions of arylboronic acids and aryl chlorides.. Isolation and structural characterization of (P,O)-Pd(dba) complex [J]. Journal of Organic Chemistry, 1999,64(18) .. 6797-6803.
  • 3FEUERSTEIN M,LAURENTI D, BOUGEANT C, et al. Palladium-tetraphosphinecatalysed cross coupling of aryl bromides with arylboronic acids: Remarkable influence of the nature of the ligand[J]. Chemical Communications, 2001 (4) : 325-326.
  • 4BENAYI.IA M, PUGLISI A, COZZI F. Polymer-supported organic catalysts[J]. Chemical Reviews, 2003, 103 (9): 3401-3430.
  • 5CATHERINE A M, DIXON J M, BRADLEY M. Recoverable catalysts and reagents using recyclable polystyrene- based supports[J]. Chemical Reviews, 2002,102 (10) : 3275-3300.
  • 6POLSHETIWAR V, LUQUE R, FIHRI A, et al. Magnetically recoverble nanocatalysts [J]. Chemical Reviews, 2011,111(5) : 3036-3075.
  • 7DHITAL R N, KAMONSATIKUL C, SAKURAI H. Low-temperature carbon-chlorine bond activation by bimetal- lic gold/palladium alloy nanoclusters: An application to ullmann coupling[J]. Journal of American Chemical Socie- ty, 2012,134(50) : 20250-20253.
  • 8HERRMANN W A, REISINGE C P, SPIEGLER M. Chelating N-heterocyclic carbene ligands in palladium-cata- lyzed heck-type reactions[J]. Journal of Organometallic Chemistry, 1998,557 (1) .. 93-96.
  • 9XU Hong, LONGLAN C, NAIHU H, et al. Developmentof magnetization FesO4/polystryrene/silica nanospheres via combined miniemulsion/emulsion polymerization[J]. Journal of American Chemical Society, 2006, 128 (49): 15582-15583.
  • 10JAFARPOUR L, STEVENS E D, NOLAN S P. A sterically demanding nucleophiliccarbene: 1,3-bis(2,6-diisopro- pylphenyl) imidazol-2-ylidene). Thermochemistryand catalytic application in olefin metathesis[J]. Journal of Orga- nometallie Chemistry, 2000,606 (1) : 49-54.

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