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Catalytic performances of cross-linking humic acids supported Pd/Ni bimetallic catalyst for heck reaction

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Języki publikacji
EN
Abstrakty
EN
The cross-linking humic acids (CL-HAs), epichlorohydrin as the cross-linking reagent and the supported Pd/Ni bimetallic catalysts (CL-HAs-Pd/Ni) were prepared and characterized by IR, AAS, XPS, TEM. The effects of reaction time, temperature, base, solvent and the amount of catalyst on the properties of the catalyst were studied. These catalysts could catalyze the Heck reaction of aryl halides and substituted aryl halides with acrylic acids or styrene successfully; the yields were all above 95%.
Rocznik
Strony
22--26
Opis fizyczny
Bibliogr. 24 poz. rys., tab.
Twórcy
autor
autor
autor
autor
  • College of Chemistry & Chemical Engineering, Henan University, Kaifeng 475001, Henan, China, yccui@henu.edu.cn
Bibliografia
  • 1. Biffis, A., Zecca, M. & Basato, M. (2001). Palladium metal catalysts in Heck C-C coupling reactions. J mol Catal A Chem, 173(1-2): 249-274.DOI:10.1016/S1381-1169(01)00153-4.
  • 2. Deiters, A. & Stephen, F. M. (2004). Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis. Chem. Rev., 104 (5):2199-2238.10.1021/cr0200872.
  • 3. Irina, P. & Andrei, V. (2000). The Heck Reaction as a Sharpening Stone of Palladium Catalysis. Chem Rev, 100(8): 3009-3066.DOI:10.1021/cr9903048.
  • 4. Liu, P., Wang, L. & Li, L. M. et al. (2004). Study on the Heck Arylation Reaction Catalyzed by Chitosan-Immobilized Palladium(0) Complex. Chin J Orgc Chem, 24(1): 59-65. DOI: CNKI:SUN:YJHU.0.2004-01-010.
  • 5. Liu, D. G., Lee, J. F. & Tang, M. T. (2005). Characterization of Pt-Ru/C catalysts by X-ray absorption spectroscopy and temperature-programmed surface reaction. J Mol Catal A Chem, 231(1-2): 197-206. DOI: 10.1016/j.molcata.2005.07.011.
  • 6. Zhang, H. F., Zhang, L. & Cui, Y. Ch. (2007). Synthesis of chitosan microsphere-resin supported palladium complex and its catalytic properties for Mizoroki-Heck reaction. React. Funct. Polym., 67(4): 322-328. DOI: 10.1016/j.reactfunctpolym.2007.01.004.
  • 7. Zhang, L. & Cui, Y C. (2005). Synthesis of Starch Supported Palladium Catalyst and Its Catalytic Properties for Heck Reaction. Chin J Appl CHem, 22(4): 440-445. DOI: CNKI:SUN:YYHX.0.2005-04-00J.
  • 8. Sun, Q., Zhang, Zh. Q. & Su, Y. Ch. et al. (1994). The Best Catalytic Condition of Multi-Nuclear Pd(?)-Ni(?) Phthalocyanine for Heck Reaction Selected with Orthogonal Test. J. Northeast Normal University, 2(2): 53-56. DOI: CNKI:SUN:DBSZ.0.1994-02-013.
  • 9. Reddy, R. K., Kumar, N. S. & Surendra, P. R. et al. (2006). Cellulose supported palladium(0) catalyst for Heck and Sonogashira coupling reactions. J Mol. Catal. A. Chem., 252(1-2): 12-16. DOI: 10.1016/j.molcata. 2006.02.024.
  • 10. Klavins, M. J. & Dipane, K. B. (2001). Influence of colloid suspensions of humic acids upon the alkaline fading of carbocations. Chemosphere, 21(7-8): 555-560. DOI: 10.1002/poc.1317.
  • 11. Klavins, M. J. & Babre, K. (2002). Decarboxylation and alkaline colour fading reactions in presence of humic substances. Chemosphere, 49(6): 685-689. DOI: 10.1016/S0045-6535(02)00303-X.
  • 12. Bellamy, L. J., The infrared spectra of complex molecules[M]. Chapman and Hall, London, 1975.
  • 13. Stevenson, F. J. Humus chemistry: genesis, composition, reactions [M]. Wiley-interscience, New York, 1994.
  • 14. Fan, K. N. An introduction of spectroscopy[M]. Higher education press, Bei Jing, 2001.
  • 15. Fujita, S., Yoshida, T. & Bhanage, B. M. et al. (2002). Heck reaction with a silica-supported Pd-TPPTS liquid phase catalyst: effects of reaction conditions and various amines on the reaction rate. J Mol Catal A Chem, 188(1-2): 37-43. DOI: 10.1016/S1381-1169(02)00336-9.
  • 16. Iweta, P. R., Anna, M. T. & Jozef, J. Z. (2006). Basefree efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide. J Mol Catal A Chem, 257, 3-8. DOI: 10.1016/j.molcata.2006.03.064.
  • 17. Li, R. X. Green solvent (the synthesis and application of ion liquid) [M]. Chemical industry press, 2004.
  • 18. Zhang, L. & Cui, Y. C. (2005). Synthesis of Polyvinyl Chloride-triethylene-tetramine Supported Pal- ladium Complex and Its Catalytic Properties for Heck Reaction. Acta Chimica Sinica, 10: 924-930. DOI: CNKI:SUN:HXXB.0.2005-10-009.
  • 19. Jiang, J. Z. & Cai, C. (2006). In situ formation of dispersed palladium nanoparticles in microemulsion: Efficient reaction system for ligand-free Heck reaction. J Collid Interf Sci, 2006, 299(2): 938-943. DOI: 10.1016/j.jcis.2006.02.035.
  • 20. Perez, R., Veronese, D. & Coelho, F. (2006). Palladium catalyzed Heck reaction of arenediazonium tetrafluoroborate salts with Baylis-Hillman adducts: production of α-benzyl-β-keto esters. Tetrahedron Lett, 47(8): 1325-1328. DOI: 10.1016/j.tetlet.2005.12.058.
  • 21. Chen, F. X., Kelvin, T. & Shen, Sh. C. et al. (2007). Porous magnesia as solid base for ligand-free Heck reaction. Catal Commun, 8(3): 405-409. DOI: 10.1016/j.catcom.2006.06.032.
  • 22. Cai, M. Zh., Xu, Q. H. & Jiang, J. W. (2006). The first MCM-41-supported thioether palladium(0) complex: A highly active and stereoselective catalyst for Heck arylation of olefins with aryl halides. J Mol Catal A Chem, 260(1-2): 190-196. DOI: 10.1016/j.molcata.2006.07.014.
  • 23. Sun, Q., Yao, X. H., Su, Y. Ch. et al. (1994). Catalytic Study on Heck Reaction by Multi-nuclear Pd(?) Ni(?)(1:1) Phthalocyanine. J Synthetic Chem, 2(3), 282-286. DOI: CNKI:SUN:HCHX.0.1994-03-015.
  • 24. Reetz, M. T., Breinbauer, R., Wanninger, K. (1996). Suzuki and Heck reactions catalyzed by preformed palladium clusters and palladium/nickel bimetallic clusters. Tetrahedron Lett, 37(26): 4499-4502. DOI: 10.1016/0040-4039(96)00924-0.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPS2-0053-0005
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