Fate of the RAFT End-Group in the Thermal Depolymerization of Polymethacrylates

被引:19
作者
Hafliger, Florian [1 ]
Truong, Nghia P. [1 ,2 ]
Wang, Hyun Suk [1 ]
Anastasaki, Athina [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Mat, Lab Polymer Mat, CH-8093 Zurich, Switzerland
[2] Monash Univ, Monash Inst Pharmaceut Sci, Parkville, Vic 3152, Australia
基金
欧洲研究理事会;
关键词
FRAGMENTATION CHAIN TRANSFER; RADICAL POLYMERIZATION; POLYMERS;
D O I
10.1021/acsmacrolett.3c00418
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Thermal RAFT depolymerization has recently emerged as a promising methodology for the chemical recycling of polymers. However, while much attention has been given to the regeneration of monomers, the fate of the RAFT end-group after depolymerization has been unexplored. Herein, we identify the dominant small molecules derived from the RAFT end-group of polymethacrylates. The major product was found to be a unimer (DP = 1) RAFT agent, which is not only challenging to synthesize using conventional single-unit monomer insertion strategies, but also a highly active RAFT agent for methyl methacrylate, exhibiting faster consumption and yielding polymers with lower dispersities compared to the original, commercially available 2-cyano-2-propyl dithiobenzoate. Solvent-derived molecules were also identified predominantly at the beginning of the depolymerization, thus suggesting a significant mechanistic contribution from the solvent. Notably, the formation of both the unimer and the solvent-derived products remained consistent regardless of the RAFT agent, monomer, or solvent employed.
引用
收藏
页码:1207 / 1212
页数:6
相关论文
共 37 条
  • [1] [Anonymous], 2008, HDB RAFT POLYM
  • [2] Elucidation of the 1,4-dioxane decomposition pathway at discrete ultrasonic frequencies
    Beckett, MA
    Hua, I
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (18) : 3944 - 3953
  • [3] Light-accelerated depolymerization catalyzed by Eosin Y
    Bellotti, Valentina
    Parkatzidis, Kostas
    Wang, Hyun Suk
    Watuthanthrige, Nethmi De Alwis
    Orfano, Matteo
    Monguzzi, Angelo
    Truong, Nghia P. P.
    Simonutti, Roberto
    Anastasaki, Athina
    [J]. POLYMER CHEMISTRY, 2023, 14 (03) : 253 - 258
  • [4] Fast Bulk Depolymerization of Polymethacrylates by ATRP
    Bossa, Ferdinando De Luca
    Yilmaz, Gorkem
    Matyjaszewski, Krzysztof
    [J]. ACS MACRO LETTERS, 2023, 12 (08) : 1173 - 1178
  • [5] Bioapplications of RAFT Polymerization
    Boyer, Cyrille
    Bulmus, Volga
    Davis, Thomas P.
    Ladmiral, Vincent
    Liu, Jingquan
    Perrier, Sebastien
    [J]. CHEMICAL REVIEWS, 2009, 109 (11) : 5402 - 5436
  • [6] 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
  • [7] Sequence-definition from controlled polymerization: the next generation of materials
    De Neve, Jeroen
    Haven, Joris J.
    Maes, Lowie
    Junkers, Tanja
    [J]. POLYMER CHEMISTRY, 2018, 9 (38) : 4692 - 4705
  • [8] Hydroperoxide Traces in Common Cyclic Ethers as Initiators for Controlled RAFT Polymerizations
    Eggers, Steffen
    Abetz, Volker
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2018, 39 (07)
  • [9] Reversible-addition fragmentation chain transfer (RAFT) mediated depolymerization of brush polymers
    Flanders, Michael J.
    Gramlich, William M.
    [J]. POLYMER CHEMISTRY, 2018, 9 (17) : 2328 - 2335
  • [10] RAFT-mediated, visible light-initiated single unit monomer insertion and its application in the synthesis of sequence-defined polymers
    Fu, Changkui
    Huang, Zixuan
    Hawker, Craig J.
    Moad, Graeme
    Xu, Jiangtao
    Boyer, Cyrille
    [J]. POLYMER CHEMISTRY, 2017, 8 (32) : 4637 - 4643