OALib Journal期刊
ISSN: 2333-9721
费用:99美元
|
|
|
[N^N^O]钴配合物催化丁二烯立体选择性聚合的研究
DOI: 10.11777/j.issn1000-3304.2015.15193, PP. 1486-1492
Keywords: 钴,倍半乙基氯化铝,丁二烯,聚合,顺式含量
Abstract:
合成并表征了一系列带有[2-(4,5-二苯基-2-咪唑基)-1-苯亚胺基]苯酚配体([N^N^O]三齿配体)的二氯化钴配合物(1~4),并研究了这些配合物对丁二烯溶液聚合的催化性能.研究结果表明,助催化剂的种类对丁二烯聚合的催化活性和产物性能有显著的影响,倍半乙基氯化铝(EASC)为最佳的助催化剂.在EASC的活化作用下,该催化体系引发丁二烯单体聚合,15min内丁二烯单体的转化率可达92.7%,产物聚丁二烯中顺式1,4-结构的含量高达97.4%.并详细研究了助催化剂的用量、聚合的温度、配体上不同取代基等对丁二烯聚合行为的影响,包括丁二烯单体的转化率、产物聚丁二烯的分子量与分子量分布及微观结构.通过凝胶渗透色谱法(GPC)对聚合产物的分子量及分子量分布进行了表征,核磁共振氢谱(1H-NMR)和碳谱(13C-NMR)分析结果表明所得聚合物具有高的顺式1,4-结构含量(97%左右).
References
[1] | 1 Porri L,Giarrusso A, Ricci G.Prog Polym Sci,1991,16:405~441
|
[2] | 2 Porri L,Giamsso A.In:Conjugated diene polymerization in comprehensive polymer science.Vol.4,Pergamon,Oxford,1989,pp.53~108
|
[3] | 3 Van Amerongen G J.Adv Chem Ser,1966,52:136~152
|
[4] | 4 Cooper W.Ind Eng Chem Prod Res Develop,1970,9:457~466
|
[5] | 5 Furukawa J.Pure Appl Chem,1975,42:495~508
|
[6] | 6 Furukawa J.Acc Chem Res,1980,13:1~6
|
[7] | 7 Oehme A,Gebauer U,Gehrke K,Lechner M D.Angew Makromol Chem,1996,235:121~130
|
[8] | 8 Proto A,Capacchione C,In:Stereoselective Polymerization with Single-site Catalysts.Boca Raton:CRC Press,2008.447~473
|
[9] | 9 Ricci G,Sommazzi A,Masi F,Ricci M,Boglia A,Leone G.Coord Chem Rev,2010,254:661~676
|
[10] | 16 Leone G,Boglia A,Bertini F,Canetti M,Ricci G.J Polym Sci Part A Polym Chem,2010,48:4473~4483
|
[11] | 17 Chandran D,Kwak C H,Ha C S,Kim I.Catal Today,2008,131:505~512
|
[12] | 18 Jia X,Liu H,Hu Y,Dai Q,Bi J,Bai C,Zhang X.Chin J Catal,2013,34:1560~1569
|
[13] | 19 Appukuttan V,Zhang L,Ha J Y,Chandran D,Bahuleyan B K,Ha C S,Kim I.J Mol Catal A Chem,2010,325:84~90
|
[14] | 20 Nobbs J D,Tomov A K,Cariou R,Gibson V C,White A J P,Britovsek G J P.Dalton Trans,2012,41:5949~5964
|
[15] | 21 Liu H,Jia X,Wang F,Dai Q,Wang B,Bi J,Zhang C,Zhao L,Bai C,Hu Y,Zhang X.Dalton Trans,2013,42:13723~13732
|
[16] | 22 Alnajrani M N,Mair F S.Dalton Trans,2014,43:15727~15736
|
[17] | 23 Jie S,Ai P,Li B G.Dalton Trans,2011,40:10975~10982
|
[18] | 24 Ai P,Chen L,Guo Y,Jie S,Li B G.J Organomet Chem,2012,705:51~58
|
[19] | 25 Ai P,Chen L,Jie S,Li B G.J Mol Catal A Chem,2013,380:1~9
|
[20] | 26 Chen L,Ai P,Gu J,Jie S,Li B G.J Organomet Chem,2012,716:55~61
|
[21] | 27 Zhou Q,Li B G,Jie S,Zheng N.Catal Sci Technol,2014,4:773~779
|
[22] | 28 Sharma S,Saha B,Sawant D,Kundu B.Synthesis,2006,1841~1847
|
[23] | 29 Cariou R,Chirinos J J,Gibson V C,Jacobsen G,Tomov A K,Britovsek G J P,White A J P.Dalton Trans,2010,39:9039~9045
|
[24] | 30 Resconi L,Camurati I,Sudmeijer O.Top Catal,1999,7:145~163
|
[25] | 31 Kwang G,Bae C,Kim S.J Appl Polym Sci,2009,113:2186~2190
|
[26] | 32 Endo K,Kitagawa T,Nakatani K.J Polym Sci Part A:Polym Chem,2006,44:4088~4094
|
[27] | 10 Cai Z,Shinzawa M,Nakayama Y,Shiono T.Macromolecules,2009,42:7642~7643
|
[28] | 11 Nath D C D,Shiono T,Ikeda T.Macromol Chem Phys,2002,203:756~760
|
[29] | 12 Nath D C D,Shiono T,Ikeda T.Appl Catal A Gen,2003,238:193~199
|
[30] | 13 Ricci G,Forni A,Boglia A,Motta T,Zannoni G,Canetti M,Bertini F.Macromolecules,2005,38:1064~1070
|
[31] | 14 Ricci G,Motta T,Boglia A,Alberti E,Zetta L,Bertini F,Arosio P,Famulari A,Meille S V.Macromolecules,2005,38:8345~8352
|
[32] | 15 Ricci G,Boglia A,Motta T,Bertini F,Boccia A C,Zetta L,Alberti E,Famulari A,Arosio P,Meille S V.J Polym Sci Part A Polym Chem,2007,45:5339~5353
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|