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新型含氮三齿钯(Ⅱ)配合物的合成及其催化性能研究 被引量:3

Synthesis of a New Pd(Ⅱ) Complex with Tridentate Nitrogen Ligands and Investigation of Its Catalytic Property
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摘要 以白屈氨酸为原料,经酯化、还原、溴化、胺化等反应合成了4位带活性基团的新型含氮(NN'N)三齿配体,配体进一步与氯化钯反应制得了Pd(II)的配合物,并用红外、核磁、元素分析等手段进行了表征.考察了这种钳形配合物的催化性能,结果表明该配合物对卤代苯与乙烯基化合物的Heck芳基化反应具有较高的催化活性. A new tridentate nitrogen ligand with a 4-position substituted active functional group in the pyridine ring was successfully prepared from chelidamic acid via the processes of esterification, reduction, bromization and amination, and then further reacted with palladium chloride to give the palladium(Ⅱ) complex. The complex was characterized by IR, ^1H, ^13C NMR spectra, elementary analysis etc. The catalytic properties of the new pincer-type NN'N complex for Heck arylation of aryl halides with alkenes were investigated. The results showed that the complex had high catalytic activities.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2007年第1期134-137,共4页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No.20576052) 江苏省自然科学基金(No.03KJA530040)资助项目.
关键词 Heck芳基化反应 三齿配体 钯配合物 催化剂 Heck arylation reaction tridentate ligand Pd complex catalyst
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参考文献21

  • 1Heck,R.F.Org.React.1982,27,345.
  • 2Heck,R.F.Acc.Chem.Res.1979,12,146.
  • 3Bergbreiter,D.E.; Osburn,P.L.; Liu,Y.S.J.Am.Chem.Soc.1999,121,9531.
  • 4张仰明,杨帆,郑瑞,汤杰.叔胺类环钯化合物在催化Heck反应中的应用[J].有机化学,2001,21(7):533-534. 被引量:1
  • 5Herrmann,W.A.; Bohm,V.P.W.; Reisinger,C.P.J.Organomet.Chem.1999,576,23.
  • 6Pelagattia,P.; Carcellia,M.; Costab,M.; Ianellia,S.; Pelizzia,C.; Rogolinoa,D.J.Mol.Catal.A:Chem.2005,226,107.
  • 7Kawano,T.; Shinomaru,T.; Ueda,I.Org.Lett.2002,4,2545.
  • 8Adrian,J.C.Jr.; Hassib,L.; DeKimpe,N.; Keppens,M.Tetrahedron 1998,54,2365.
  • 9Constable,E.C.; Kulke,T.; Neuburger,M.; Zehnder,M.New J.Chem.1997,21,1091.
  • 10Welch,T.W.; Ciftan,S.A.; White,P.S.; Thorp,H.H.Inorg.Chem.1997,36,4812.

二级参考文献9

  • 1[1]Heck, R. F. Palladium Reagents in Organic Synthesis, Academic Press, London, 1985.
  • 2[2]Herrmann, W. A.; Bohm, V. P. W.; Reisinger, C. P. J.Organomet. Chem.1999, 576, 23.
  • 3[3]Ohff, M.; Ohff, A.; Milstein, D. Chem. Commun.1999,357.
  • 4[4]Cope, A. C.; Friedrich, E. C. J. Am. Chem. Soc.1968,90,909.
  • 5[5]Crociani, B.; Boschi, T.; Pietropaolo, R.; Belluco, U. J.Chem. Soc. (A) 1970, 53, 1
  • 6[6]Gaunt, J. C.; Shaw, B. L. J. Organomet. Chem. 1975,102, 511.
  • 7[7]100 mL of standard solution 1 was prepared by dissolving 0.0014 g (2.5 × 10-3 mmol) of complex 1 in CH2Cl2. 100 mL of standard solution 2 was prepared by diluting 1mL of solution 1 with CH2Cl2. For every experiment, 1mL of standard solution 2 was transferred to a flask and the solvent was evaporated in vacuum.
  • 8[8]Miyazaki, F.; Yamaguchi, K.; Shibasaki, M. Tetrahedron Lett.1999, 40, 7379.
  • 9[9]Ozawa, F.; Kubo, A.; Hayashi, T. Chem. Lett. 1992,2177.

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