Construction of Autonomic Self-Healing CO2-Based Polycarbonates via One-Pot Tandem Synthetic Strategy

被引:44
作者
Yang, Guan-Wen [1 ]
Zhang, Yao-Yao [1 ]
Wang, Yanyan [2 ]
Wu, Guang-Peng [1 ]
Xu, Zhi-Kang [1 ]
Darensbourg, Donald J. [2 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Lab Macromol Synth & Functionalizat Adsorpt, Hangzhou 310027, Zhejiang, Peoples R China
[2] Texas A&M Univ, Dept Chem, 3255 TAMU, College Stn, TX 77843 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; CARBON-DIOXIDE; POLY(PROPYLENE CARBONATE); TRIBLOCK COPOLYMERS; PROPYLENE-OXIDE; CO2; CATALYSTS; EPOXIDES; POLYMERS; WATER;
D O I
10.1021/acs.macromol.7b02715
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The coupling of epoxides and carbon dioxide to polycarbonates (CO2-PCs) has been the subject of intense research for nearly half a century. Although tremendous progress has been achieved, their aliphatic characteristics and lack of timctionalities of CO2-PCs limit the scope of their application in high value-added and functional materials. In this article, the first CO2-based polycarbonate with the ability to autonomously self-heal is constructed via a one-pot synthetic strategy. The key to the success of the synthetic strategy is efficient tandem three different catalytic reactions, i.e., hydrolysis of epoxides, immortal copolymerization of CO2/epoxides, and thiol-ene click reactions one-pot process. Based on the standard tensile testing,, these CO2-based materials show robust self healing properties, where the extensibility maximal strength, and Young's modulus of the specimens can almost entirely recover to their original value under ambient temperature. Our studies demonstrate that the self-healing capability of these CO2-based materials, arises both from the homo-hydrogen bonding (between amide groups) and the hetero-hydrogen bonding (between amide group and carbonate group of polycarbonate backbone). The convenient and atom economic synthesis strategy, combined with the impressive self-healing capability for these materials, should expand the library of high value-added CO2-based polycarbonates and the scope of their applications.
引用
收藏
页码:1308 / 1313
页数:6
相关论文
共 54 条
  • [1] Recent strategies to develop self-healable crosslinked polymeric networks
    An, So Young
    Arunbabu, Dhamodaran
    Noh, Seung Man
    Song, Young Kyu
    Oh, Jung Kwon
    [J]. CHEMICAL COMMUNICATIONS, 2015, 51 (66) : 13058 - 13070
  • [2] Bottenbruch L., 1996, ENG THERMOPLASTICS, P112
  • [3] Metal-Catalyzed Transesterification for Healing and Assembling of Thermosets
    Capelot, Mathieu
    Montarnal, Damien
    Tournilhac, Francois
    Leibler, Ludwik
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (18) : 7664 - 7667
  • [4] Chen YL, 2012, NAT CHEM, V4, P467, DOI [10.1038/NCHEM.1314, 10.1038/nchem.1314]
  • [5] New generation polymers: the role of metal alkoxides as catalysts in the production of polyoxygenates
    Chisholm, MH
    Zhou, ZP
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (21) : 3081 - 3092
  • [6] Discrete metal-based catalysts for the copolymerization CO2 and epoxides:: Discovery, reactivity, optimization, and mechanism
    Coates, GW
    Moore, DR
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (48) : 6618 - 6639
  • [7] Malleable and Self-Healing Covalent Polymer Networks through Tunable Dynamic Boronic Ester Bonds
    Cromwell, Olivia R.
    Chung, Jaeyoon
    Guan, Zhibin
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (20) : 6492 - 6495
  • [8] Copolymerization of CO2 and epoxides catalyzed by metal salen complexes
    Darensbourg, DJ
    Mackiewicz, RM
    Phelps, AL
    Billodeaux, DR
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2004, 37 (11) : 836 - 844
  • [9] Catalysts for the reactions of epoxides and carbon dioxide
    Darensbourg, DJ
    Holtcamp, MW
    [J]. COORDINATION CHEMISTRY REVIEWS, 1996, 153 : 155 - 174
  • [10] Making plastics from carbon dioxide:: Salen metal complexes as catalysts for the production of polycarbonates from epoxides and CO2
    Darensbourg, Donald J.
    [J]. CHEMICAL REVIEWS, 2007, 107 (06) : 2388 - 2410