四丁基碘化铵催化甲基丙烯酸甲酯的可逆-休眠自由基溶液聚合
|
摘要
以四丁基碘化铵(BNI)为有机催化剂,碘单质(I2)与偶氮二异庚腈(ABVN)原位生成的碘代异庚腈为引发剂,进行甲基丙烯酸甲酯(MMA)的溶液聚合.以甲苯为溶剂,MMA∶I2∶ABVN的摩尔比为200∶1∶1. 7,考察了催化剂用量对聚合的影响.结果表明,加入催化剂可以缩短诱导期,当I2∶BNI摩尔比为1∶1时聚合反应的诱导期最短(1. 7 h);当BNI∶I2摩尔比为0. 25∶1～2∶1之间时,聚合物实测分子量与理论值十分接近,分子量分布较窄,分子量分布指数(Mw/Mn)多在1. 2以下.考察了在N,N'-二甲基甲酰胺(DMF)、四氢呋喃(THF)、苯甲醚、苯和甲苯5种溶剂中的聚合反应,发现在苯和甲苯中聚合可控性最佳,Mw/Mn多在1. 2以下;苯甲醚和THF中聚合速率较快,聚合物分子量分布较苯中的略宽.以DMF为溶剂时所得聚合物分子量分布很宽,聚合可控性差.核磁共振分析聚合物为碘封端结构,碘原子封端的聚合物链所占比为91. 6%.
Tetrabutylammonium iodide( BNI) has been found to be a highly efficient organic catalyst for the reversible-deactivation radical polymerization( RDRP) of methyl methacrylate with an in situ formed alkyl iodine initiator. The polymerization results exhibited typical features of "living "/controlled radical polymerization. The polymerization process efficiently controls the molecular weight and chemical structure of the poly( methyl methacrylate)( PMMA). Furthermore, the inhibition period was shortened and the polymerization rate was increased upon the addition of BNI as compared to blank controls. The effect of BNI contents on the controllability of MMA polymerization was also investigated in detail. The results showed that good agreement between theoretical and experimental molar masses( characterized by GPC) was observed for the used molar ratio of I2 to BNI( 1 ∶ 2,1 ∶ 1,1 ∶ 0. 5,1 ∶ 1 and 1 ∶ 0). The molar ratio of n( MMA) ∶n( I2) ∶ n( ABVN) ∶ n( BNI) = 200 ∶ 1 ∶ 1. 7 ∶ 1 is an optimum formula affording polymers with predetermined molecular weight and low-polydispersity polymers( Mw/Mn< 1. 2) at relatively high polymerization rate. The polymerizations of MMA in different solvents were carried out. The polymerizations have good control effect in toluene and benzene( Mw/Mn< 1. 2). The molecular structure and the chain end fidelity of the obtained low-molecular-weight PMMA( Mn,GPC= 3300,Mw/Mn= 1. 15) prepared by reversible complexation mediated polymerization( RCMP) were demonstrated by1 H NMR spectrum. The calculated Mn,NMRwas in good agreement with Mn,thand the fraction of iodine chain end of the PMMA chains was up to 91. 6%.
Tetrabutylammonium iodide( BNI) has been found to be a highly efficient organic catalyst for the reversible-deactivation radical polymerization( RDRP) of methyl methacrylate with an in situ formed alkyl iodine initiator. The polymerization results exhibited typical features of "living "/controlled radical polymerization. The polymerization process efficiently controls the molecular weight and chemical structure of the poly( methyl methacrylate)( PMMA). Furthermore, the inhibition period was shortened and the polymerization rate was increased upon the addition of BNI as compared to blank controls. The effect of BNI contents on the controllability of MMA polymerization was also investigated in detail. The results showed that good agreement between theoretical and experimental molar masses( characterized by GPC) was observed for the used molar ratio of I2 to BNI( 1 ∶ 2,1 ∶ 1,1 ∶ 0. 5,1 ∶ 1 and 1 ∶ 0). The molar ratio of n( MMA) ∶n( I2) ∶ n( ABVN) ∶ n( BNI) = 200 ∶ 1 ∶ 1. 7 ∶ 1 is an optimum formula affording polymers with predetermined molecular weight and low-polydispersity polymers( Mw/Mn< 1. 2) at relatively high polymerization rate. The polymerizations of MMA in different solvents were carried out. The polymerizations have good control effect in toluene and benzene( Mw/Mn< 1. 2). The molecular structure and the chain end fidelity of the obtained low-molecular-weight PMMA( Mn,GPC= 3300,Mw/Mn= 1. 15) prepared by reversible complexation mediated polymerization( RCMP) were demonstrated by1 H NMR spectrum. The calculated Mn,NMRwas in good agreement with Mn,thand the fraction of iodine chain end of the PMMA chains was up to 91. 6%.
引文
[1] Otsu T.,Yoshida M.,Macromolecular Rapid Communications,1982,26(3),127—132
[2] Georges M. K.,Veregin R. P. N.,Kazmaier P. M.,Hamer G. K.,Macromolecules,1993,26(11),2987—2988
[3] Wang J. S.,Matyjaszewski K.,Journal of the American Chemical Society,1995,117(20),5614—5615
[4] Chiefari J.,Chong Y. K.,Ercole F.,Krstina J.,Jeffery J.,Le T. P. T.,Mayadunne R. T. A.,Meijs G. F.,Moad C. L.,Moad G.,Rizzardo E.,Thang S. H.,Macromolecules,1998,31(16),5559—5562
[5] Joseph R.,Pallan P S.,Sudalai A.,Ravindranathan T.,Tetrahedron Letters,1995,36(4),609—612
[6] Goto A.,Fukuda T.,Ohno K.,Macromolecules,1998,31(9),2809—2814
[7] Clerc S.,Tonnar J.,Lacroix-Desmazes P.,European Polymer Journal,2013,49(3),682—692
[8] Boyer C.,Lacroix-Desmazes P.,Jeanjacques R. A.,Boutevin B.,Macromolecules,2006,39(12),4044—4053
[9] Kim K.,Na R. K.,Rhee S. E.,Lee B. H.,Choe S.,Polymer,2012,53(19),4054—4059
[10] Goto A.,Zushi H.,Hirai N.,Kwak Y.,Fukuda T.,ACS Symposium Series,2006,944(40),595—603
[11] Goto A.,Wakada T.,Fukuda T.,Tsujii Y.,Macromolecular Chemistry&Physics,2010,211(5),594—600
[12] Goto A.,Zushi H.,Hirai N.,Wakada T.,Kwak Y.,Fukuda T.,Macromolecular Symposia,2007,248(1),126—131
[13] Goto A.,Hirai N.,Tsujii Y.,Fukuda T.,Macromolecular Symposia,2008,261(1),18—22
[14] Goto A.,Hirai N.,Tsujii Y.,Fukuda T.,Polymer,2008,49(24),5177—5185
[15] Goto A.,Hirai N.,Wakada T.,Nagasawa K.,Tsujii Y.,Fukuda T.,Macromolecules,2008,41(17),6261—6264
[16] Kim J.,Nomura A.,Fukuda T.,Goto A.,Tsujii Y.,Macromolecular Reaction Engineering,2010,4(3/4),272—277
[17] Wang C. G.,Hanindita F.,Goto A.,ACS Macro Letters,2018,7(2),263—268
[18] Goto A.,Sanada S.,Lei L.,Hori K.,Macromolecules,2016,49(7),2511—2517
[19] Wang C. G.,Goto A.,Journal of the American Chemistry Society,2017,139(30),10551—10560
[20] Sarkar J.,Xiao L.,Goto A.,Macromolecules,2016,49(14),5033—5042
[21] Lei L.,Tanishima M.,Goto A.,Hironori K.,Multidisciplinary Digital Publishing Institute,2014,6(3),860—872
[22] Goto A.,Ohtsuki A.,Ohfuji H.,Tanishima M.,Hironori K.,Journal of the American Chemical Society,2013,135(30),11131—11139
[23] Lacroix-Desmazes P.,Severac R.,Boutevin B.,Macromolecules,2005,38(38),6299—6309
[24] Wang Y. A.,Shi Y.,Fu Z. F.,Yang W. T.,Polymer Chemistry,2017,8(39),6073—6085
[25] Chen K. L.,Hui J.,Shi Y.,Yang W. T.,Fu Z. F.,Acta Polymerica Sinica,2016,(1),111—117(陈珂龙,惠嘉,石艳,杨万泰,付志峰.高分子学报,2016,(1),111—117)
[26] Braunecker W. A.,Itami Y.,Matyjaszewski K.,Macromolecules,2005,38(23),9402—9404
[27] Bai L.,Wang W.,Chen H.,Wang M.,Cheng Z.,RSC Advances,2015,5(44),34769—34776
[2] Georges M. K.,Veregin R. P. N.,Kazmaier P. M.,Hamer G. K.,Macromolecules,1993,26(11),2987—2988
[3] Wang J. S.,Matyjaszewski K.,Journal of the American Chemical Society,1995,117(20),5614—5615
[4] Chiefari J.,Chong Y. K.,Ercole F.,Krstina J.,Jeffery J.,Le T. P. T.,Mayadunne R. T. A.,Meijs G. F.,Moad C. L.,Moad G.,Rizzardo E.,Thang S. H.,Macromolecules,1998,31(16),5559—5562
[5] Joseph R.,Pallan P S.,Sudalai A.,Ravindranathan T.,Tetrahedron Letters,1995,36(4),609—612
[6] Goto A.,Fukuda T.,Ohno K.,Macromolecules,1998,31(9),2809—2814
[7] Clerc S.,Tonnar J.,Lacroix-Desmazes P.,European Polymer Journal,2013,49(3),682—692
[8] Boyer C.,Lacroix-Desmazes P.,Jeanjacques R. A.,Boutevin B.,Macromolecules,2006,39(12),4044—4053
[9] Kim K.,Na R. K.,Rhee S. E.,Lee B. H.,Choe S.,Polymer,2012,53(19),4054—4059
[10] Goto A.,Zushi H.,Hirai N.,Kwak Y.,Fukuda T.,ACS Symposium Series,2006,944(40),595—603
[11] Goto A.,Wakada T.,Fukuda T.,Tsujii Y.,Macromolecular Chemistry&Physics,2010,211(5),594—600
[12] Goto A.,Zushi H.,Hirai N.,Wakada T.,Kwak Y.,Fukuda T.,Macromolecular Symposia,2007,248(1),126—131
[13] Goto A.,Hirai N.,Tsujii Y.,Fukuda T.,Macromolecular Symposia,2008,261(1),18—22
[14] Goto A.,Hirai N.,Tsujii Y.,Fukuda T.,Polymer,2008,49(24),5177—5185
[15] Goto A.,Hirai N.,Wakada T.,Nagasawa K.,Tsujii Y.,Fukuda T.,Macromolecules,2008,41(17),6261—6264
[16] Kim J.,Nomura A.,Fukuda T.,Goto A.,Tsujii Y.,Macromolecular Reaction Engineering,2010,4(3/4),272—277
[17] Wang C. G.,Hanindita F.,Goto A.,ACS Macro Letters,2018,7(2),263—268
[18] Goto A.,Sanada S.,Lei L.,Hori K.,Macromolecules,2016,49(7),2511—2517
[19] Wang C. G.,Goto A.,Journal of the American Chemistry Society,2017,139(30),10551—10560
[20] Sarkar J.,Xiao L.,Goto A.,Macromolecules,2016,49(14),5033—5042
[21] Lei L.,Tanishima M.,Goto A.,Hironori K.,Multidisciplinary Digital Publishing Institute,2014,6(3),860—872
[22] Goto A.,Ohtsuki A.,Ohfuji H.,Tanishima M.,Hironori K.,Journal of the American Chemical Society,2013,135(30),11131—11139
[23] Lacroix-Desmazes P.,Severac R.,Boutevin B.,Macromolecules,2005,38(38),6299—6309
[24] Wang Y. A.,Shi Y.,Fu Z. F.,Yang W. T.,Polymer Chemistry,2017,8(39),6073—6085
[25] Chen K. L.,Hui J.,Shi Y.,Yang W. T.,Fu Z. F.,Acta Polymerica Sinica,2016,(1),111—117(陈珂龙,惠嘉,石艳,杨万泰,付志峰.高分子学报,2016,(1),111—117)
[26] Braunecker W. A.,Itami Y.,Matyjaszewski K.,Macromolecules,2005,38(23),9402—9404
[27] Bai L.,Wang W.,Chen H.,Wang M.,Cheng Z.,RSC Advances,2015,5(44),34769—34776