Has Click Chemistry Lead to a Paradigm Shift in Polymer Material Design?

被引:108
作者
Barner-Kowollik, Christopher [1 ]
Inglis, Andrew J. [1 ]
机构
[1] Univ Karlsruhe TH, Inst Tech Chem & Polymerchem, KIT, D-76128 Karlsruhe, Germany
关键词
Click Chemistry; material design; polymer design; ONE-POT SYNTHESIS; BLOCK-COPOLYMERS; TRIBLOCK COPOLYMERS; FUNCTIONALIZED POLYMERS; MODULAR SYNTHESIS; AMIDE SYNTHESIS; VINYL-ACETATE; CYCLOADDITION; COMBINATION; ALKYNE;
D O I
10.1002/macp.200900139
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Has the introduction of the click chemistry concept by Sharpless and colleagues in 2001 lead to a paradigm shift in how we approach the design of macromolecular materials; or is it simply a relatively inconsequential re-branding exercise of already existing and slightly optimized but well-tried and tested reactions as some critics would have it? The current Trend Article analyses the situation by examining a series of select macromolecular research fields to shed light on this question, providing an unambiguous answer: The focusing of polymer chemists through the click concept on what constitutes a powerful modular chemical transformation to generate a specific polymeric material is a defining element in contemporary synthetic polymer chemistry, transcending a specific reaction. Without the introduction of the click philosophy several classes of innovative materials and polymer designs would not have been realized.
引用
收藏
页码:987 / 992
页数:6
相关论文
共 29 条
  • [1] A versatile synthetic approach to polypeptide based rod-coil block copolymers by click chemistry
    Agut, Willy
    Taton, Daniel
    Lecommandoux, Sebastien
    [J]. MACROMOLECULES, 2007, 40 (16) : 5653 - 5661
  • [2] [Anonymous], ANGEW CHEM
  • [3] [Anonymous], 1962, The structure of scientifc revolutions
  • [4] 'Click' chemistry in polymer and material science: An update
    Binder, Wolfgang H.
    Sachsenhofer, Robert
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2008, 29 (12-13) : 952 - 981
  • [5] Practical synthesis of amides from in situ generated copper(I) acetylides and sulfonyl azides
    Cassidy, Michael P.
    Raushel, Jessica
    Fokin, Valery V.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (19) : 3154 - 3157
  • [6] Rate-accelerated nonconventional amide synthesis in water: A practical catalytic aldol-surrogate reaction
    Cho, Seung Hwan
    Chang, Sukbok
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (11) : 1897 - 1900
  • [7] Copper-catalyzed hydrative amide synthesis with terminal alkyne, sulfonyl azide, and water
    Cho, SH
    Yoo, EJ
    Bae, L
    Chang, S
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (46) : 16046 - 16047
  • [8] Addition-fragmentation kinetics of fluorodithioformates (F-RAFT) in styrene, vinyl acetate, and ethylene polymerization: An ab initio investigation
    Coote, Michelle L.
    Izgorodina, Ekaterina I.
    Cavigliasso, German E.
    Roth, Marion
    Busch, Markus
    Barner-Kowollik, Christopher
    [J]. MACROMOLECULES, 2006, 39 (13) : 4585 - 4591
  • [9] Preparation of block copolymers via diels alder reaction of maleimide- and anthracene-end functionalized polymers
    Durmaz, H
    Colakoclu, B
    Tunca, U
    Hizal, G
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (05) : 1667 - 1675
  • [10] One-pot synthesis of ABC type triblock copolymers via in situ click [3+2] and Diels-Alder [4+2] reactions
    Durmaz, Hakan
    Dag, Aydan
    Altintas, Ozcan
    Erdogan, Tuba
    Hizal, Gurkan
    Tunca, Umit
    [J]. MACROMOLECULES, 2007, 40 (02) : 191 - 198