Solid-supported MADIX polymerization of vinyl acetate

被引:33
作者
Nguyen, Due H. [2 ]
Wood, Murray R. [1 ]
Zhao, Youliang [1 ]
Perrier, Sebastien [1 ]
Vana, Philipp [2 ]
机构
[1] Univ Leeds, Dept Colour & Polymer Chem, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ma801328c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A simple, one-pot synthesis of a surface-tethered MADIX agent was established via the reaction of 1,1'-thiocarbonyl diimidazole (TCDI) with a thiol, followed by reaction with, the hydroxyl groups of a Wang resin. The supported RAFT agent was used to control the polymerization of vinyl acetate in toluene. The amount of surface-bound polymer was found to greatly increase with increasing content of solid MADIX agent, reaching values of almost 80%. The grafted PVAc chains were cleaved from the Wang resin support via radical reaction with tert-amyl peroxy acetate TAPA), and the molecular weight distributions exhibited the typical shape of polymers formed via a well-controlled living radical polymerization (LRP), with the free polymers showing a slightly higher molecular weight than the living fraction. The M-n values of both living polymer fraction (surface-bound polymer) and dead polymer (free polymer) increased steadily with monomer conversion-as expected for a well controlled MADIX polymerization-and were in good agreement with the theoretical molecular weights. PDI values of both polymer fractions scatter around 1.5, with a slight tendency of narrower molecular weight distributions of the living polymer, which shows a minimum value of 1.43. Addition of free MADIX agent to the solution phase led to a decrease in PDI values of both free and bound polymer, and. the experimental molar masses were in very good agreement with theoretical predictions.
引用
收藏
页码:7071 / 7078
页数:8
相关论文
共 55 条
[1]  
ADVINCULA RC, 2004, POLYM BRUSHES SYNTHE, pR23
[2]   Cumyl dithiobenzoate mediated RAFT polymerization of styrene at high temperatures [J].
Arita, T ;
Buback, M ;
Vana, P .
MACROMOLECULES, 2005, 38 (19) :7935-7943
[3]   Reversible addition-fragmentation chain transfer polymerization initiated with γ-radiation at ambient temperature:: an overview [J].
Barner, L ;
Quinn, JF ;
Barner-Kowollik, C ;
Vana, P ;
Davis, TP .
EUROPEAN POLYMER JOURNAL, 2003, 39 (03) :449-459
[4]   RAFTing down under: Tales of missing radicals, fancy architectures, and mysterious holes [J].
Barner-Kowollik, C ;
Davis, TP ;
Heuts, JPA ;
Stenzel, MH ;
Vana, P ;
Whittaker, M .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (03) :365-375
[5]   Mechanism and kinetics of dithiobenzoate-mediated RAFT polymerization. I. The current situation [J].
Barner-Kowollik, Christopher ;
Buback, Michael ;
Charleux, Bernadette ;
Coote, Michelle L. ;
Drache, Marco ;
Fukuda, Takeshi ;
Goto, Atsushi ;
Klumperman, Bert ;
Lowe, Andrew B. ;
Mcleary, James B. ;
Moad, Graeme ;
Monteiro, Michael J. ;
Sanderson, Ronald D. ;
Tonge, Matthew P. ;
Vana, Philipp .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (20) :5809-5831
[6]   Synthesis of polymer brushes on silicate substrates via reversible addition fragmentation chain transfer technique [J].
Baum, M ;
Brittain, WJ .
MACROMOLECULES, 2002, 35 (03) :610-615
[7]   Pressure dependence of the propagation rate coefficient kp for vinyl acetate polymerizations in bulk and in solution of fluid CO2 [J].
Beuermann, S ;
Buback, M ;
Nelke, D .
MACROMOLECULES, 2001, 34 (19) :6637-6640
[8]   Poly(vinyl acetate) and poly(vinyl propionate) star polymers via reversible addition fragmentation chain transfer (RAFT) polymerization [J].
Boschmann, D ;
Vana, P .
POLYMER BULLETIN, 2005, 53 (04) :231-242
[9]   Initiation of radical polymerization by peroxyacetates:: Polymer end-group analysis by electrospray ionization mass spectrometry [J].
Buback, Michael ;
Frauendorf, Holm ;
Guenzler, Fabian ;
Vana, Philipp .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (12) :2453-2467
[10]  
Charmot D, 2000, MACROMOL SYMP, V150, P23, DOI 10.1002/1521-3900(200002)150:1<23::AID-MASY23>3.0.CO