A circular polyester platform based on simple gem-disubstituted valerolactones

被引:84
|
作者
Li, Xin-Lei [1 ]
Clarke, Ryan W. [2 ]
Jiang, Jing-Yang [1 ]
Xu, Tie-Qi [1 ]
Chen, Eugene Y-X [2 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, Dept Chem, State Key Lab Fine Chem, Dalian, Peoples R China
[2] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
基金
中国国家自然科学基金;
关键词
MACROMOLECULAR SCIENCE VIEWPOINT; RING-OPENING POLYMERIZATION; 100TH ANNIVERSARY; FUTURE; POLYMERS; WASTE;
D O I
10.1038/s41557-022-01077-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Geminal disubstitution of cyclic monomers is an effective strategy to enhance the chemical recyclability of their polymers, but it is utilized for that purpose alone and often at the expense of performance properties. Here we present synergistic use of gem-alpha,alpha-disubstitution of available at-scale, bio-based delta-valerolactones to yield gem-dialkyl-substituted valerolactones (VLR2), which generate polymers that solve not only the poor chemical recyclability but also the low melting temperature and mechanical performance of the parent poly(delta-valerolactone); the gem-disubstituted polyesters (PVLR2) therefore not only exhibit complete chemical recyclability but also thermal, mechanical and transport properties that rival or exceed those of polyethylene. Through a fundamental structure-property study that reveals intriguing impacts of the alkyl chain length on materials performance of PVLR2, this work establishes a simple circular, high-performance polyester platform based on VLR2 and highlights the importance of synergistic utilization of gem-disubstitution for enhancing both chemical recyclability and materials performance of sustainable polyesters.
引用
收藏
页码:278 / +
页数:11
相关论文
共 50 条
  • [1] A circular polyester platform based on simple gem-disubstituted valerolactones
    Xin-Lei Li
    Ryan W. Clarke
    Jing-Yang Jiang
    Tie-Qi Xu
    Eugene Y.-X. Chen
    Nature Chemistry, 2023, 15 : 278 - 285
  • [2] REGIOSELECTIVE REDUCTION OF GEM-DISUBSTITUTED SUCCINIMIDES
    WIJNBERG, JBPA
    SCHOEMAKER, HE
    SPECKAMP, WN
    TETRAHEDRON, 1978, 34 (02) : 179 - 187
  • [3] DIENE CONDENSATION OF GEM-DISUBSTITUTED BUTADIENES
    SOPOV, NP
    KOVNER, ML
    JOURNAL OF GENERAL CHEMISTRY USSR, 1964, 34 (05): : 1502 - &
  • [4] SYNTHESIS OF UNSYMMETRICAL, gem-DISUBSTITUTED BISAMIDES
    Schafer, Gabriel
    Len, Lukas
    Bode, Jeffrey W.
    HETEROCYCLES, 2015, 90 (02) : 1375 - 1386
  • [5] A Modular Approach to the Synthesis of gem-Disubstituted Cyclopropanes
    Harris, Michael R.
    Wisniewska, Hanna M.
    Jiao, Wenhua
    Wang, Xiaochun
    Bradow, James N.
    ORGANIC LETTERS, 2018, 20 (10) : 2867 - 2871
  • [6] REMARKABLY REGIOSELECTIVE REDUCTION OF GEM-DISUBSTITUTED SUCCINIMIDES
    WIJNBERG, JB
    SPECKAMP, WN
    SCHOEMAK.HE
    TETRAHEDRON LETTERS, 1974, (46) : 4073 - 4076
  • [7] NMR . STUDY OF STEREOCHEMISTRY OF SOME GEM-DISUBSTITUTED CYCLOPROPANES
    PLAT, M
    SEYDENPE.J
    STRZALKO, T
    BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, 1967, (10): : 3664 - &
  • [8] STEREOSELECTIVE SYNTHESIS OF GEM-DISUBSTITUTED CYCLOPROPANES FROM GEM-DIBROMOCYCLOPROPANES
    HARADA, T
    KATSUHIRA, T
    HATTORI, K
    OKU, A
    TETRAHEDRON LETTERS, 1989, 30 (44) : 6039 - 6040
  • [9] GEM-DISUBSTITUTED AMINO-ETHER BASED SUBSTANCE-P ANTAGONISTS
    HARRISON, T
    WILLIAMS, BJ
    SWAIN, CJ
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (23) : 2733 - 2734
  • [10] REACTIONS OF NITRILE YLIDS WITH OLEFINS GEM-DISUBSTITUTED WITH WITHDRAWING GROUPS
    PERROCHEAU, J
    DANIONBOUGOT, R
    CARRIE, R
    BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, 1994, 131 (09): : 973 - 985