A Novel One-Pot Procedure for the Fast and Efficient Conversion of RAFT Polymers into Hydroxy-Functional Polymers

被引:37
作者
Gruendling, Till [1 ,2 ]
Dietrich, Mathias [1 ,3 ]
Barner-Kowollik, Christopher [1 ]
机构
[1] Univ Karlsruhe TH, KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Univ New S Wales, UNSW Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Sydney, NSW 2052, Australia
[3] Fraunhofer Inst Chem Technol, Environm Engn Grp, D-76327 Pfinztal, Germany
关键词
FRAGMENTATION CHAIN TRANSFER; TRANSFER RADICAL POLYMERIZATION; DEFINED BLOCK-COPOLYMERS; ABSOLUTE RATE CONSTANTS; END-GROUP MODIFICATION; MASS-SPECTROMETRY; HYDROCARBON AUTOXIDATION; AMBIENT-TEMPERATURE; VERSATILE APPROACH; MOLECULAR-WEIGHT;
D O I
10.1071/CH09080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on the successful quantitative transformation of methacrylate and acrylate-type polymers prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization carrying a dithioester-end-group into hydroxy-functional polymers. The simple reaction procedure involves stirring a solution of the dithioester-capped polymer and an azo-initiator in tetrahydrofuran at elevated temperatures (T = 60 degrees C) in the presence of air. This reaction quantitatively yields hydroperoxide functionalities that can be efficiently reduced to hydroxy groups in a one-pot procedure using triphenylphosphine. Size exclusion chromatography-electrospray mass spectrometry was employed to monitor the progress of the reaction. The new backbone-linked hydroxy group provides a versatile anchor for chemical end-group conversions and conjugation reactions with prepared RAFT polymers, which alleviates problems with the rather limited ability of the dithioester-end-group to undergo non-radical transformations.
引用
收藏
页码:806 / 812
页数:7
相关论文
共 47 条
  • [1] A multidisciplinary approach to the use of pyridinyl dithioesters and their N-oxides as CTAs in the RAFT polymerization of styrene.: Not the chronicle of a failure foretold
    Alberti, A
    Benaglia, M
    Guerra, M
    Gulea, M
    Hapiot, P
    Laus, M
    Macciantelli, D
    Masson, S
    Postma, A
    Sparnacci, K
    [J]. MACROMOLECULES, 2005, 38 (18) : 7610 - 7618
  • [2] Complex macromolecular architectures by reversible addition fragmentation chain transfer chemistry: Theory and practice
    Barner, Leonie
    Davis, Thomas P.
    Stenzel, Martina H.
    Barner-Kowollik, Christopher
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (05) : 539 - 559
  • [3] The future of reversible addition fragmentation chain transfer polymerization
    Barner-Kowollik, Christopher
    Perrier, Sebastien
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (17) : 5715 - 5723
  • [4] BarnerKowollik C., 2008, Handbook of RAFT Polymerization
  • [5] Bednarek M, 2000, MACROMOL CHEM PHYSIC, V201, P58, DOI 10.1002/(SICI)1521-3935(20000101)201:1<58::AID-MACP58>3.0.CO
  • [6] 2-G
  • [7] Recent mechanistic developments in atom transfer radical polymerization
    Braunecker, Wade A.
    Matyjaszewski, Krzysztof
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2006, 254 (1-2) : 155 - 164
  • [8] Convergent synthesis of 3-arm star polymers from RAFT-prepared poly(N,N-diethylacrylamide) via a thiol-ene click reaction
    Chan, Justin W.
    Yu, Bing
    Hoyle, Charles E.
    Lowe, Andrew B.
    [J]. CHEMICAL COMMUNICATIONS, 2008, (40) : 4959 - 4961
  • [9] Brush-type amphiphilic diblock copolymers from "living"/controlled radical polymerizations and their aggregation behavior
    Cheng, ZP
    Zhu, XL
    Kang, ET
    Neoh, KG
    [J]. LANGMUIR, 2005, 21 (16) : 7180 - 7185
  • [10] Thermolysis of RAFT-synthesized poly(methyl methacrylate)
    Chong, Bill
    Moad, Graeme
    Rizzardo, Ezio
    Skidmore, Melissa
    Thang, San H.
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 2006, 59 (10) : 755 - 762