Polymerization of acrylonitrile catalyzed by single yttrium tris(2,6-di-tert-butyl-4-methyl phenolate)

被引:11
|
作者
Zheng, H [1 ]
Zhang, YF [1 ]
Shen, ZQ [1 ]
机构
[1] Zhejiang Univ, Inst Polymer Sci, Hangzhou 310027, Peoples R China
关键词
yttrium tris(2,6-di-tert-butyl-4-methyl-phenolate); acrylonitrile; polymerization;
D O I
10.1002/pi.933
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymerization of acrylonitrile was carried out using yttrium tris(2,6-di-tert-butyl 4-methyl-phenolate) (Y(OAr)(3)) as single component catalyst for the first time. The effects of concentrations of the monomer and catalyst, kinds of rare earth element and solvent, as well as temperature and polymerization time were investigated. The overall activation energy of polymerization in n-hexane and THF mixture is 18.3 kJ mol(-1). Polyacrylonitriles (PANs) obtained by using Y(OAr)(3) in n-hexane and THF mixture at 50degreesC are predominantly atactic, while yellow PANs obtained in DMF under the same conditions have a syndiotactic-rich configuration (>50%), and their highly branched and/or cyclized structures have also been found. (C) 2002 Society of Chemical Industry.
引用
收藏
页码:622 / 626
页数:5
相关论文
共 50 条
  • [31] Spin-lattice and spin-spin relaxation times of 2,4,6-tri-tert-butyl phenoxyl and 2,6-di-tert-butyl-4-methyl phenoxyl in diamagnetic crystals:: Relaxation mechanism and influence of molecular motions
    Yamauchi, J
    Yamaji, T
    Katayama, A
    APPLIED MAGNETIC RESONANCE, 2003, 25 (02) : 209 - 216
  • [32] Block copolymerization of 2,2-dimethyltrimethylene carbonate with adipic anhydride catalyzed by lanthanum tris(2,6-di-tert-butyl-4-methylphenolate)
    Ling, Jun
    Ren, Shijian
    Shen, Zhiquan
    E-POLYMERS, 2010,
  • [33] Block copolymerization of 2,2-dimethyltrimethylene carbonate with adipic anhydride catalyzed by lanthanum tris(2,6-di-tert-butyl-4-methylphenolate)
    Ling J.
    Ren S.
    Shen Z.
    E-Polymers, 2010,
  • [34] BASE-CATALYZED REARRANGEMENT OF 4-METHYL-4-ACETOXY-2,6-DI-TERT-BUTYL-2,5-CYCLOHEXADIENONE
    CHASAR, DW
    JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (16): : 3363 - 3364
  • [35] ε-Caprolactone Polymerization under Air by the Biocatalyst: Magnesium 2,6-Di-tert-butyl-4-Methylphenoxide
    Fang, Hsin-Jou
    Lai, Ping-Shan
    Chen, Jia-Yun
    Hsu, Sodio C. N.
    Peng, Wei-De
    Ou, Siou-Wei
    Lai, Yi-Chun
    Chen, Yen-Jen
    Chung, Hsuan
    Chen, Yun
    Huang, Ta-Chou
    Wu, Bo-Sheng
    Chen, Hsuan-Ying
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (13) : 2697 - 2704
  • [36] OXIDATION OF HINDERED PHENOLS .5. THE 2,6-DI-TERT-BUTYL-4-ISOPROPYL AND 2,6-DI-TERT-BUTYL-4-SEC-BUTYLPHENOXY RADICALS
    COOK, CD
    NORCROSS, BE
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (15) : 3797 - 3799
  • [37] Ring-opening polymerization of 1,4-dioxan-2-one initiated by lanthanum tris(2,6-di-tert-butyl-4-methylphenolate)
    Fang, Qing
    Zheng, Hao
    Shen, Guo-rong
    Shen, Zhi-quan
    CHINESE JOURNAL OF POLYMER SCIENCE, 2007, 25 (04) : 427 - 430
  • [38] PHOTOCHEMICAL PROCESSES OF 2,6-DI-TERT-BUTYL-4-METHYLPHENOL
    NOWAKOWSKA, M
    KOWAL, J
    EUROPEAN POLYMER JOURNAL, 1980, 16 (07) : 615 - 618
  • [39] 2,6-Di-tert-butyl-4-(morpholinomethyl)phenol monohydrate
    Zeng, Tao
    Ren, Wan-Zhong
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2008, 64 : O406 - U2017
  • [40] Polymerization characteristics of ε-caprolactone at low temperature by lanthanum tris(2,6-di-tert-butyl-4-methylphenolate) and the block copolymerization of ε-caprolactone with cyclic carbonates
    Zhu, GX
    Tan, GH
    Ling, J
    Chen, W
    Shen, ZQ
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2006, 27 (02): : 356 - 359