References
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Bellamy, L. J., The infrared spectra of complex molecules[M]. Chapman and Hall, London, 1975.
- Stevenson, F. J. Humus chemistry: genesis, composition, reactions [M]. Wiley-interscience, New York, 1994.
- Fan, K. N. An introduction of spectroscopy[M]. Higher education press, Bei Jing, 2001.
- 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.
- 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.
- Li, R. X. Green solvent (the synthesis and application of ion liquid) [M]. Chemical industry press, 2004.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.