A novel synthetic method for well-defined polymers containing benzotriazole and diazobenzene chromophores

被引:9
作者
Sun, Bin [1 ]
Zhu, Xiulin [1 ]
Zhu, Han [1 ]
Cheng, Zhenping [1 ]
Zhang, Zhengbiao [1 ]
机构
[1] Suzhou Univ, Sch Chem & Chem Engn, Key Lab Organ Synth Jiangsu Prov, Suzhou 215006, Peoples R China
关键词
azobenzene; benzotriazoles; photoisomerization; postfunctionalization; reversible addition-fragmentation chain transfer (RAFT) polymerization;
D O I
10.1002/macp.200700040
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
PBHEMA was prepared by RAFT polymerization in the presence of CPDN and AIBN. Diazobenzene groups were introduced into the sidechains by post-azo-functionalization. The resulting polymers containing benzotriazol and azobenzene groups exhibited higher molecular weight than original polymers, narrow MWD (M-W/M-n=1.17-1.26) degrees of functionality. Thermal stabilities and glass transition temperatures of the polymers increased with the introduction of diazo chromophores. The molecular weight of the polymer had a slight effect on the T-g of the polymer. The polymer showed partial crystallization as the diazo content increased above 36%. [GRAPHICS]
引用
收藏
页码:1101 / 1109
页数:9
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  • [1] Synthesis and characterization of segmented liquid crystalline polymers with the azo group in the main chain
    Acierno, D
    Amendola, E
    Bugatti, V
    Concilio, S
    Giorgini, L
    Iannelli, P
    Piotto, SP
    [J]. MACROMOLECULES, 2004, 37 (17) : 6418 - 6423
  • [2] Complex molecular architecture polymers via RAFT
    Barner, L
    Barner-Kowollik, C
    Davis, TP
    Stenzel, MH
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 2004, 57 (01) : 19 - 24
  • [3] RAFTing down under: Tales of missing radicals, fancy architectures, and mysterious holes
    Barner-Kowollik, C
    Davis, TP
    Heuts, JPA
    Stenzel, MH
    Vana, P
    Whittaker, M
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (03) : 365 - 375
  • [4] Honeycomb-structured porous films from polypyrrole-containing block copolymers prepared via RAFT polymerization as a scaffold for cell growth
    Beattie, D
    Wong, KH
    Williams, C
    Poole-Warren, LA
    Davis, TP
    Barner-Kowollik, C
    Stenzel, MH
    [J]. BIOMACROMOLECULES, 2006, 7 (04) : 1072 - 1082
  • [5] BRAWN CEH, 1960, T FARADAY SOC, V56, P815
  • [6] Mechanism of dithiobenzoate-mediated RAFT polymerization: A missing reaction step
    Buback, Michael
    Vana, Philipp
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2006, 27 (16) : 1299 - 1305
  • [7] Synthesis and characterization of polyurethane anionomers with bisazoaromatic chrornophores and carboxylate groups
    Buruiana, T
    Buruiana, EC
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  • [8] Living free-radical polymerization by reversible addition-fragmentation chain transfer: The RAFT process
    Chiefari, J
    Chong, YK
    Ercole, F
    Krstina, J
    Jeffery, J
    Le, TPT
    Mayadunne, RTA
    Meijs, GF
    Moad, CL
    Moad, G
    Rizzardo, E
    Thang, SH
    [J]. MACROMOLECULES, 1998, 31 (16) : 5559 - 5562
  • [9] Thiocarbonylthio compounds [S=C(Ph)S-R] in free radical polymerization with reversible addition-fragmentation chain transfer (RAFT polymerization). Role of the free-radical leaving group (R)
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    Krstina, J
    Le, TPT
    Moad, G
    Postma, A
    Rizzardo, E
    Thang, SH
    [J]. MACROMOLECULES, 2003, 36 (07) : 2256 - 2272
  • [10] Thermotropic side-chain liquid crystalline copolymers containing both mono- and bisazobenzene mesogens: Synthesis and properties
    Cojocariu, C
    Rochon, P
    [J]. MACROMOLECULES, 2005, 38 (23) : 9526 - 9538