20 10 2008 10 PROGRESS IN CHEMISTRY Vol. 20 No. 10 Oct., 2008 N2 3 1 1 1 3 3 2 (1. 200092 ; 2. 200433) N2,, 2 (RAFT) (MADIX), ( ),, (ATRP) N2 : O632. 1 : A : 10052281X(2008) 1021572206 Living Radical Polymerization of N2Vinylamides Pu Hongting 1 Cai Xiangyu 1 Wan Decheng 1 3 3 Yang Genjin 2 (1. Institute of Functional Polymers, School of Materials Science & Engineering, Tongji University, Shanghai 200092, China ; 2. School of Pharmacy, The Second Military Medical University, Shanghai 200433, China) Abstract The progress regarding the living radical polymerization of N2vinylamides (NVAs) is summarized. The living radical polymerization of the unconjugated NVAs once represented a synthetic challenge, but pleasant progress has been made recently in this field. It is found that selected members of the xanthate family and dithiocarbamate family are able to control the polymerization of NVAs via reversible addition2fragmentation chain transfer ( RAFT) polymerization or via the interchange of xanthate (MADIX) under certain conditions, and the tacticity can be simultaneously controlled under specific conditions. The recently developed organobismuth, organostibine and organotellurium compounds are effective mediators for the ( co ) polymerization of most NVAs, expanding the spectra of polymer composition. Additionally, some of the atom transfer radical polymerization (ATRP) systems are applicable to the polymerization of NVAs. Key words N2vinylamides ; living radical polymerization ; organobismuth ; organostibine ; organotellurium 1 N2, N2 (NVF), N2 (NVP) N2 (NVCL), 1,PNVP [1 ] 1 N2 Fig. 1 Chemical structure of several typical N2vinylamides : 2007 11, : 2007 12 3 985 (No. 0502144002) 3 3 e2mail :wandecheng @mail. tongji. edu. cn
10 N2 1573 ; (PEO) 1939,,,, 100,, N2 N2 [1 ], PNVCL,, N2 ( PNIPAM), 32 PNIPAM, PNVCL PNVP,, PNIPAM N2, [1 ], PNVP PNVP,, 2 RAFTΠMADIX,, N2,, 1993 Georges [2 ] (NMP) [3 ], [4 (ATRP) 6 ], [7 2 (RAFT) 9 ] ( MADIX [10 ], RAFT ), N2,,,, N2, 1998 [11 ],, 2002,, N2 RAFTΠMADIX 2 [7,8,10 ] 2 RAFTΠMADIX [7,8,10 ] Fig. 2 Mechanism of RAFTΠMADIX RAFTΠMADIX
1574 20 [12, 16 ] 1 ( Z R ), 2,Z R 3 N2 RAFTΠMADIX ZC( [12 S) SR 18 ] Fig. 3 Chain transfer agents ZC( = S) SR employed in RAFTΠ [12 MADIX polymerization of N2vinylamides 18 ] 2003, [17 ] (PEO) ( 1a, 3), 100 PEO2 PNVF,, (PDI) 117 2005, [18 ] 1b, 1c 1j, NVP RAFTΠMADIX, 1c, PDI 1110 1126 : (1) ; (2), 1j 1, ( ) ( ) 2,5,, ; (3) 1b, 1c, 1c 1b, R NVP,R, [19,20 ] R, ( ) ( ) : R ( ) 2 3 1 2 ( ) P m P n,, 1 [21 ] ; (4), PNVP 1c,, Devasia [22 ] 1e NVP RAFTΠMADIX, 111 116 ( ), 2 P m R ( R PNVP),,,, P m P n,,,,,,, PNVP Stenzel [19 ], 1b, 1c PNVP Moad [23 ] 1f PNVP,, Klumperman [21 ] 1g NVP 1g,,, 2 ( ), RAFTΠMADIX,1h, NVP,, 1i R,,NVP N2, [24 ] RAFTΠMADIX,, NVP, NVP NVCL [20 ],NVCL
10 N2 1575 ( GPC) (MALTI2TOF),,, GPC MALTI2TOF PNVCL, 1b 1c 1d 1c, 1b 1d, PDI 1150,,,, 1d PDI 1124 ( MALTI2TOF ), 1c NVP, NVCL,,, N2, N2,,, Yamago NVP ( NVCL ), [ 25 3 TERP SBRP BIRP 31], 3 NMP ATRP RAFTΠMADIX,, ATRP RAFTΠ MADIX,, 2002,Yamago [27 29 ], [30,31 ] [25 ] (TERP) (SBRP) (BIRP) 4 [25 31 ] Fig. 4 Chemical compounds of organotellurium,organostibine and organobismuthine that used in living radical [25 polymerization 31 ], 2a 2c 2d 2f 2g 2h, 100, 30 60 BIRP > SBRP > TERP BIRP, : (1) ( ), ; (2) NVP 2g NVP [25 ], 60 000,PDI 1112 ; (3), [26 ],, (MMA) NVP ( ) [31 ], 2d, AIBN (AIBN 0125 ), 60, PMMA ( M n = 4 700,
1576 20 PDI = 1127), PMMA2b2PNVP (, M n = 20 500, PDI = 1131), PNVP( M n = 3 000, PDI = 1. 06), PNVP2b2PMMA (, M n = 20 400, PDI = 1. 18),,TERP SBRP BIRP NVP Π [25,27,30,31 ], BIRP > SBRP > TERP, 112 (Me 6 Cyclam),, NVP,, PDI 112 113 (NMP), Hadjichristidis [38,39 ], NVP,, N2? 5 [25 ],,,, (, 5 ), k ex,, P P,,,, BIRP > SBRP > TERP >, 5 [25 ] Fig. 5 Schematic mechanism of organobismuthine2mediated living radical polymerization [25 ], [32,33 ],, 4 ATRP,, N2,, ATRP,, Debuigne [34 ], NVP [35 ],, PDI 1130 Matyjaszewski [36 ] NVP,, PDI 117 Meng [37 ] 5,5,7,12,12,142 21,4,8,, N2 Π ( RAFTΠMADIX ) ( BIRP SBRP TERP ) ATRP,,,, [ 1 ] Kirsh Y E. Water Soluble Poly2N2Vinylamides, Synthesis and Physicochemical Properties. Chichester : John Wiley & Sons, 1998 [ 2 ] Georges M K, Veregin R P N, Kazmaier P M, et al. Macromolecules, 1993, 26 : 2987 2988 [ 3 ] Hawker C J, Bosman A W, Harth E. Chem. Rev., 2001, 101 : 3661 3688 [ 4 ] Matyjaszewski K, Xia J. Chem. Rev., 2001, 101 : 2921 2990 [ 5 ] Kamigaito M, Ando T, Sawamoto M. Chem. Rev., 2001, 101 : 3689 3745 [ 6 ] Percec V, Barboiu B. Macromolecules, 1995, 28 : 7970 7972 [ 7 ] Chiefari J, Chong Y K, Ercole F, et al. Macromolecules, 1998, 31 : 5559 5561
10 N2 1577 [ 8 ] Le T P, Moad G, Rizzardo E, et al. Australia, PCT Int. Appl. WO 9 801 4782A [ 9 ] Moad G, Rizzardo E, Thang S H. Austra. J. Chem., 2006, 59 : 669 692 [10] Destarac M, Bzducha W, Taton D, et al. Macromol. Rapid. Commun., 2002, 23 : 1049 1054 [11] Chiefari J, Mayadunne R T A, Moad G, Rizzardo E, Thang S H. WO 9 931 1442A [12] ( Ge X P), (Bai R K), (Progress in Chemistry), 2007, 19(9) : 1406 1412 [13] Lowe A B, McCormick C L. Prog. Polym. Sci. 2007, 32 : 283 351 [14] Barner L, Davis T P, Stenzel M H, Barner2Kowollik C. Macromol. Rapid Commu., 2007, 28 : 539 559 [15] Moad G, Rizzardo E, Thang S H. Polymer, 2008, 49 : 1079 1131 [16] Moad G, Rizzardo E, Thang S H. Australian J. Chem., 2006, 59 : 669 692 [17] Shi L J, Chapman T M, Beckman E J. Macromolecules, 2003, 36 : 2563 2567 [18] Wan D C, Satoh K, Kamigaito M, et al. Macromolecules, 2005, 38 : 10397 10405 [19] Nguyen T L U, Eagles K, Stenzel M H, et al. J. Polym. Sci., Part A : Polym. Chem., 2006, 44 : 4372 4383 [20] Wan D C, Zhou Q, Pu H T, et al. J. Polym. Sci., Part A : Poly. Chem., 2008, 46 : 3756 3765 [21] Pound G, McLeary J B, McKenzie J M, Lange R F M, Klumperman B. Macromolecules, 2006, 39 : 7796 7797 [22] Devasia R, Bindu R L, Borsali R, et al. Macromol. Symp., 2005, 229 : 8 17 [23] Postma A, Davis T P, Moad G, et al. Macromolecules, 2006, 39 : 5307 5318 [24] Devasia R, Borsali R, Lecommandoux S, et al. Abstract of Papers of the American Chemcial Society, 2005, 230 : U4231 U4232 [25] Yamago S, Kayahara E, Kotani M, et al. Angew. Chem. Int. Ed., 2007, 46 : 1304 1306 [26] Yamago S. J. Polym. Sci., Part A : Polym. Chem., 2006, 44 : 1 12 [27] Yusa S, Yamago S, Sugahara M, et al. Macromolecules, 2007, 40 : 5907 5915 [28] Yamago S, Iida K, Yoshida J. J. Am. Chem. Soc., 2002, 124 : 2874 2875 [29] Yamago S, Iida K, Yoshida J. J. Am. Chem. Soc., 2002, 124 : 13666 13667 [30] Yamago S, Ray B, Iida K, et al. J. Am. Chem. Soc., 2004, 126 : 13908 13909 [31] Ray B, Kotani M, Yamago S. Macromolecules, 2006, 39 : 5259 5265 [32] Curran D P. in Comprehensive Organic Synthesis. Vol. 4 (eds. : Trost B M. Fleming I). Oxford : Pergamon, 1991. 715 831 [33] Renaud P, Sibi M P. Radicals in Organic Synthesis. Weinheim : Wiley2VCH. 2001 [34] Debuigne A, Caille J R, Jerome R. Angew. Chem. Int. Ed., 2005, 44 : 1101 1104 [35] Debuigne A, Willet N, Jerome R, et al. Macromolecules, 2007, 40 : 7111 7118 [36] Kaneyoshi H, Matyjaszeski K. Macromolecules, 2006, 39 : 2757 2763 [37] Lu X J, Gong S L, Meng L Z, et al. Polymer, 2007, 48 : 2835 2842 [38] Bilalis P, Pitsilalis M, Hadjichristidis N. J. Polym. Sci. Part A : Polym. Chem., 2006, 44 : 659 665 [39] Bilalis P, Zorba G, Pitsilalis M, Hadjichristidis N. J. Polym. Sci. Part A : Polym. Chem., 2006, 44 : 5719 5728