Preparation of fluorinated polyesters by reversible addition-fragmentation chain transfer step-growth polymerization

被引:2
|
作者
Mei, Gaohuai [1 ]
Lei, Shujing [1 ]
Li, Qili [1 ]
Xu, Jianquan [1 ]
Huo, Meng [1 ]
机构
[1] Zhejiang Sci Tech Univ, Dept Chem, Hangzhou 310018, Peoples R China
关键词
COPOLYMERS; POLYMERS; LACTONES; LIQUID; WATER;
D O I
10.1039/d4py00156g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Fluorinated polyesters have demonstrated significant research value and application prospects, while their traditional synthetic strategies were restrained by harsh reaction conditions, low monomer activity, and limited polymer topology. Herein, we exploited reversible addition-fragmentation chain transfer (RAFT) step-growth polymerization to prepare fluorinated polyesters with tailor-made chemical compositions and correlated their thermal and surface properties with chemical structures. A model polymerization was first performed using the fluorinated bifunctional chain transfer agent (CTA) BDMAT8F and N,N '-(1,4-phenylene)dimaleimide as the monomers, and the polymerization kinetics was monitored through nuclear magnetic resonance (NMR) spectroscopy and size exclusion chromatography (SEC), which suggested a step-growth polymerization mechanism. With this method, fluorinated polyesters with different chemical structures were synthesized by varying the molecular structures of the bifunctional CTA and the bismaleimide monomer. The chemical structure and molecular weight of the synthesized fluorinated polyesters were characterized by 1H NMR, 19F NMR, and SEC, the thermal properties were characterized by thermogravimetric analyses and differential scanning calorimetry, and the surface properties were characterized by water contact angle (WCA) measurements. The glass transition temperature (Tg) of these fluorinated polyesters was correlated with their chemical structures, where a rigid backbone favored a high Tg, while a flexible pendant group decreased the Tg. However, neither the backbone rigidity nor the fluorine content had an obvious effect on the WCA of the fluorinated polyesters. Instead, the pendant group showed a significant influence on their WCA. The unique advantage of RAFT step-growth polymerization for preparing fluorinated polyesters was demonstrated by the preparation of a novel fluorinated polyester brush by grafting copolymerization of acryloylmorpholine through RAFT radical polymerization from an as-synthesized fluorinated polyester. Both the thermal and surface properties of this fluorinated polyester brush were strongly correlated with the properties of the poly(acryloylmorpholine) sidechains. This method has provided a new platform for the preparation of fluorinated polyesters and will provide new insight for tailoring the properties of polyesters. Reversible addition-fragmentation chain transfer (RAFT) step-growth polymerization was exploited to prepare fluorinated polyesters, and their thermal and surface properties were correlated with the chemical structures.
引用
收藏
页码:1234 / 1243
页数:10
相关论文
共 50 条
  • [31] Detailed study of the reversible addition-fragmentation chain transfer polymerization and co-polymerization of 2-methacryloyloxyethyl phosphorylcholine
    Bhuchar, Neha
    Deng, Zhicheng
    Ishihara, Kazuhiko
    Narain, Ravin
    POLYMER CHEMISTRY, 2011, 2 (03) : 632 - 639
  • [32] Quantitative preparation of multiblock glycopolymers bearing glycounits at the terminal segments by aqueous reversible addition-fragmentation chain transfer polymerization of acrylamide monomers
    Nagao, Masanori
    Hoshino, Yu
    Miura, Yoshiko
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2019, 57 (08) : 857 - 861
  • [33] Preparation of core-shell molecularly imprinted polymer via the combination of reversible addition-fragmentation chain transfer polymerization and click reaction
    Chang, Limin
    Li, Ying
    Chu, Jia
    Qi, Jingyao
    Li, Xin
    ANALYTICA CHIMICA ACTA, 2010, 680 (1-2) : 65 - 71
  • [34] Controlled Synthesis of Block Copolymers containing N-isopropylacrylamide by Reversible Addition-Fragmentation Chain-Transfer (RAFT) Polymerization
    Vega-Rios, Alejandro
    Licea-Claverie, Angel
    JOURNAL OF THE MEXICAN CHEMICAL SOCIETY, 2011, 55 (01) : 21 - 32
  • [35] Reversible Addition-Fragmentation Chain Transfer Polymerization Implemented as Continuous Process in CSTR and PFR at Elevated Reaction Conditions
    Koch, Sara C.
    Busch, Markus
    CHEMIE INGENIEUR TECHNIK, 2011, 83 (10) : 1720 - 1727
  • [36] Direct Radical Polymerization of Vinyl Ethers: Reversible Addition-Fragmentation Chain Transfer Polymerization of Hydroxy-Functional Vinyl Ethers
    Sugihara, Shinji
    Kawamoto, Yuki
    Maeda, Yasushi
    MACROMOLECULES, 2016, 49 (05) : 1563 - 1574
  • [37] Visible Light Induced Rapid Reversible Addition-fragmentation Chain Transfer Polymerization (RAFT) of Styrene at Room Temperature
    Luo Juxiang
    Cheng Deshu
    Li Mingchun
    Xin Meihua
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2018, 39 (04): : 800 - 806
  • [38] Switchable Reversible Addition-Fragmentation Chain Transfer (RAFT) Polymerization in Aqueous Solution, N,N-Dimethylacrylamide
    Keddie, Daniel J.
    Guerrero-Sanchez, Carlos
    Moad, Graeme
    Rizzardo, Ezio
    Thang, San H.
    MACROMOLECULES, 2011, 44 (17) : 6738 - 6745
  • [39] Enabling Reversible Addition-Fragmentation Chain-Transfer Polymerization for Brush Copolymers with a Poly(2-oxazoline) Backbone
    Kim, Jungyeon
    Cattoz, Beatrice
    Leung, Alice H. M.
    Parish, James D.
    Becer, C. Remzi
    MACROMOLECULES, 2022, 55 (11) : 4411 - 4419
  • [40] Chiral Self-Assembly of Nanoparticles Induced by Polymers Synthesized via Reversible Addition-Fragmentation Chain Transfer Polymerization
    Cheng, Guiqing
    Xu, Duo
    Lu, Zhongyuan
    Liu, Kun
    ACS NANO, 2019, 13 (02) : 1479 - 1489