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Cationic ring-opening polymerization of 3,3-bis(chloromethyl)oxacyclobutane in ionic liquids 被引量:1

Cationic ring-opening polymerization of 3,3-bis(chloromethyl)oxacyclobutane in ionic liquids
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摘要 Cationic ring-opening polymerization of 3,3-bis(chloromethyl)oxacyclobutane catalyzed by BF3.OEt2 was carded out in ionic liquids [bmim]BF4 and [bmim]PF6. The influences of BCMO concentration and molar ratio of BCMO/BF3.OEt2 on the molecular weights and yield of PBCMO were investigated. The polymerization in ionic liquids proceed to high conversions, although molecular weights are limited, similar to polymerization in organic solvent such as CH2Cl2. Follow a viewpoint of green chemistry, we feel ionic liquid [bmim]BF4 is superior to [bmim]PF6. Extracting [bmim]PF6 from the product using organic solvent as extractant limits its advantage as a green reaction media. Cationic ring-opening polymerization of 3,3-bis(chloromethyl)oxacyclobutane catalyzed by BF3.OEt2 was carded out in ionic liquids [bmim]BF4 and [bmim]PF6. The influences of BCMO concentration and molar ratio of BCMO/BF3.OEt2 on the molecular weights and yield of PBCMO were investigated. The polymerization in ionic liquids proceed to high conversions, although molecular weights are limited, similar to polymerization in organic solvent such as CH2Cl2. Follow a viewpoint of green chemistry, we feel ionic liquid [bmim]BF4 is superior to [bmim]PF6. Extracting [bmim]PF6 from the product using organic solvent as extractant limits its advantage as a green reaction media.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第10期1187-1190,共4页 中国化学快报(英文版)
基金 financially supported by the Key Project of Chinese Ministry of Education(No.105075) the National Natural Science Foundation of China(No.20503016).
关键词 Ionic hquid 3 3-Bis(chloromethyl)oxacyclobutane Cationic ring-opening polymerization CHARACTERIZATION Ionic hquid 3,3-Bis(chloromethyl)oxacyclobutane Cationic ring-opening polymerization Characterization
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  • 1[1]P.T.Anastas,J.C.Warner,Green Chem.:Theory Pract.1998.
  • 2[2]V.Strehmel,A.Laschewsky,H.Wetzel,E.Gornitz,Macromology 39 (2006) 923.
  • 3[3]S.Z.Abe din,N.Borissenko,F.Endres,Electrochem.Commun.6 (2004) 422.
  • 4[4]C.P.Mehnert,Chem.Eur.J.11 (2005) 50.
  • 5[5]J.Kadokawa,Y.Iwasaki,H.Tagaya,Macromol.Rapid Commun.23 (2002) 757.
  • 6[6]Y.Y.Wang,D.Jiang,R.Wang,L.Y.Dai,React.Kinet.Catal.Lett.90 (2007) 69.
  • 7[7](a) T.Biedron,M.Bednarek,P.Kubisa,Macromol.Rapid.Commun.25 (2004) 878;(b) Y.B.Xiong,L.Fan,Z.Q.Shen,Chin.J.Catal.1 (2006) 75;(c) C.G.Sanchez,M.Lobert,R.Hoogenboom,U.S.Schubert,Macromol.Rapid Commun.28 (2007) 456.
  • 8[8](a) S.M.Zhang,Y.W.Hou,W.G.Huang,Y.K.Shan,Electrochim.Acta 50 (2005) 4097;(b) Y.Y.Wang,W.Li,C.D.Xu,L.Y.Dai,Chin.J.Chem.25 (2007) 68.
  • 9[9]P.A.Z.Suarez,J.E.L.Dullius,S.Einfont,R.F.De Souza,J.Dupont,Polyhedron 15 (1996) 1217.

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